1. Trang chủ
  2. » Giáo Dục - Đào Tạo

Role of phospholipase a2 in orofacial pain and synaptic transmission 4

41 303 0

Đang tải... (xem toàn văn)

Tài liệu hạn chế xem trước, để xem đầy đủ mời bạn chọn Tải xuống

THÔNG TIN TÀI LIỆU

Thông tin cơ bản

Định dạng
Số trang 41
Dung lượng 1,27 MB

Nội dung

Chapter Role of lysophospholipids in synaptic transmission LysoPI MBCD+lysoPI Normalized Capacitance(%) 1.08 1.04 * 1.00 0.96 30 Time(s) A LysoPI 0Ca+lysoPI Normalized Capacitance(%) 1.08 1.04 * 1.00 0.96 B 30 Time(s) Fig.2.5.3. Capacitance measurements. A: Treatment of cells with MBCD prior to addition of lysoPI resulted in attenuation of lysoPI induced exocytosis. B: Cells pre-treated with thapsigargin and recorded in zero external Ca2+ solution showed no induction of exocytosis after addition of lysoPI. *: significant difference (P < 0.05, analyzed by Student’s t-test). 5.3.3. Amperometry measurements (Fig. 2.5.4.) Infusion of lysoPI in the external solution resulted in an immediate increase in catecholamine release from PC-12 cells (132.7 ± 32.94 spikes) (Fig. 2.5.4A). This increase was markedly attenuated in cells that were pre-incubated with MBCD (3.5 ± 3.4 spikes) (Fig. 2.5.4B) or pre-treated with thapsigargin and recorded in zero Ca2+ conditions (2 ± 0.19 spikes) (Fig. 2.5.4C). These results 141 Chapter Role of lysophospholipids in synaptic transmission show that neurotransmitter release triggered by lysoPI was dependent on the integrity of cholesterol rich domains on the cell membrane and [Ca2+]i. 80 4pA 5s 60 -12 x10pA LysoPI, 10mM Ca2+ 40 20 0A 2+ LysoPI, , 20 10mM Ca40 MBCD treated 60 time (s) 80 100 120 B LysoPI, 0mM Ca2+, EGTA, thapsigargin Number of Events C D 190 150 110 70 30 -10 LysoPI MBCD+lysoPI 0Ca+lysoPI Fig.2.5.4. Amperometry measurements. A: infusion of lysoPI in the external solution resulted in an immediate increase in catecholamine release from PC-12 cells. B, C: this increase was completely abolished in cells that had been pre-incubated with MBCD (B) or Ca2+ free external solution containing the Ca2+ chelator EGTA and thapsigargin (C). D: summary results of experiments (A–C). Events are selected with spikes >2 pA for the first application of lysoPI. *: significant difference (P < 0.05, analyzed by Student’s t-test). 142 Chapter Role of lysophospholipids in synaptic transmission 5.3.4. Fura-2 measurements (Fig. 2.5.5.) LysoPI induced a sustained increase in [Ca2+]i in PC-12 cells of 1.06 ± 0.06 of normalized 340/380 ratio compared to the resting state. The increase in [Ca2+]i was markedly attenuated in cells that were pre-incubated with MBCD (1.0 ± 0.002 of normalized 340/380 ratio) or pre-treated with thapsigargin and recorded in zero Ca2+ conditions (1.0 ± 0.02 of normalized 340/380 ratio) (Fig. 2.5.5). LysoPI 0Ca+lysoPI MBCD+lysoPI Ethanol Normalized 340/380 1.10 1.06 1.02 0.98 400 800 Time(s) 1200 1600 Fig.2.5.5. Fura-2 imaging. LysoPI induced a sustained increase in [Ca2+]i in PC-12 cells. The lysoPI induced increase in [Ca2+]i was attenuated by pretreatment of cells with MBCD and by pre2+ incubation of cells with thapsigargin. No change in [Ca ]i concentration was detected after addition of ethanol (vehicle control). Arrow indicates time of addition of lysoPI. 143 Chapter Role of lysophospholipids in synaptic transmission 5.4. Discussion The present study demonstrated possible effects of lysophospholipids on exocytosis. An increase in vesicle fusion, indicating exocytosis, was observed in PC-12 cells after external infusion of the lysoPI, but not lysoPC or lysoPS by TIRFM. Similarly, external infusion of lysoPI, but not lysoPC or lysoPS induced significant increases in capacitance, or number of spikes detected by carbon fiber electrodes at amperometry, indicating exocytosis. Depletion of cholesterol by pre-incubation of cells with MBCD and depletion of Ca2+ by thapsigargin and incubation in zero external Ca2+ resulted in attenuation of lysoPI induced exocytosis, indicating that exocytosis was dependent on the integrity of lipid rafts and [Ca2+]i. Moreover, lysoPI induced a rise in [Ca2+]i suggesting that this could be the trigger for exocytosis. It is possible that lysoPI exerts it effects through binding to a lysoPI specific receptor on the cell membrane or by its physical properties on the cell membrane. A lysoPI specific receptor (GPR55) has been identified in the frontal cortex, striatum, hypothalamus, caudate putamen of the brain (Sawzdargo et al. 1999; Johns et al. 2007; Ryberg et al. 2007). In addition, lysoPI has ‘‘detergent like’’ actions and could affect the functions of ion channels or receptors on the cell membrane to cause an increase in [Ca2+]i concentration and exocytosis. The present results are consistent with previous studies which showed that lysoPI causes Ca2+ influx via store operated Ca2+ entry channels (Singaravelu et al. 2008). Moreover, lysoPI has been shown to mediate the release of insulin upon melittin (induced sPLA2) stimulation, a process which 144 Chapter Role of lysophospholipids in synaptic transmission exhibits the characteristics of physiologic exocytosis, i.e., it is reversible, saturable and does not influence subsequent islet functioning (Metz 1986). Besides lysoPI, phosphatidylinositol 4,5-bisphosphate (PtdIns (4,5)P2), a phosphoinositide found mainly in the plasma membrane also regulates exocytosis and synaptic transmission (Valtorta and Meldolesi 1994; Holz et al. 2000). PtdIns (4,5)P2 is thought to have multiple roles in exocytosis, including the establishment of secretory granule docking sites on the plasma membrane as well as participating in a step linked to fusion (Martin 2001). Moreover, glycosylphosphatidylinositol-anchored proteins in the lipid rafts of neurons are able to activate signaling pathways affecting exocytosis (Brown 2006). Previous studies have suggested a link between PLA2 and lysophospholipids in pancreatic secretion and mast cell degranulation. PLA2 and acyltransferase activities were identified in membranes associated with purified pancreatic zymogen granules. PLA2 activity was correlated to protein concentration and was Ca2+-dependent, consistent with a sPLA2 isoform. The intact zymogen granules and granule membranes demonstrated reacylating activity which was related to the concentration of lysophospholipid (Rubin et al. 1990). Similarly, PLA2 which prefers PI over PC as substrate has been detected in mast cell secretory granules. As with pancreatic zymogen granules, mast cell granules contain an active acylating system which rapidly reacylate lysoPI to form PI. These findings provide a basis for linking PLA2 activity and formation of lysophospholipids, to granule exocytosis (Chock et al. 1991). Besides lysoPI, lysoPS also provoked degranulation and histamine release in mast cells (Smith et al. 1979; Bigon et al. 145 Chapter Role of lysophospholipids in synaptic transmission 1980; Bruni et al. 1984) by enhancing stimulus-dependent Ca2+ ion influx through a specific membrane receptor (Inoue K et al. 1989). LysoPS did not cause exocytosis in PC-12 cells however. Another lysophospholipid, lysoPC also did not cause any exocytosis in PC-12 but it able to stimulate cell motility and releases pro-inflammatory cytokines. LysoPC modulates ion channel permeability in various brain preparations through at least three different mechanisms. By incorporating into neural membranes, it can perturb the orderly packing of phospholipid bilayers inducing alterations of the normal conformation of integral membrane proteins such as ion channels. Secondly, lysoPC can interact directly with ion channel proteins, and finally, lysoPC can modulate the ion channel by modulating signal transduction processes. Thus, in neurons, lysoPC produces prolonged hyperpolarization of K+ channels (Maingret et al. 2000). Under certain conditions, lysoPC also causes cell fusion. Thus, lysoPC may be involved in cell-cell and membrane-membrane interactions and neurotransmitter release (Farooqui and Horrocks 2006). The findings of a role of lysoPI in exocytosis may be important from the standpoint of the function of sPLA2 in neuroendocrine cells. Previous studies showed that external application of sPLA2-IIA (crotoxin B or purified human synovial sPLA2) to PC-12 cells and cultured rat hippocampal neurons resulted in an immediate increase in exocytosis and neurotransmitter release. EGTA and a specific inhibitor of sPLA2 activity, 12-epi-scalaradial, completely abolished the increase in neurotransmitter release, indicating that the effect of sPLA2 was dependent on Ca2+ and sPLA2 enzymatic activity (Wei et al. 2003). These 146 Chapter Role of lysophospholipids in synaptic transmission findings suggest that sPLA2 may have a role in exocytosis and neurotransmitter release in neuroendocrine cells and neurons. In recent findings (in chapter 4), it showed high levels of sPLA2-IIA expression in the brainstem and spinal cord. sPLA2-IIA protein was found in the brainstem, cervical, thoracic and lumbar spinal segments by Western blots. The enzyme was localized by immunohistochemistry to neuronal cell bodies and dendrites in the spinal trigeminal nucleus and the dorsal and ventral horns of the spinal cord. Electron microscopy of the spinal cord showed that sPLA2-IIA was localized in dendrites or dendritic spines that were postsynaptic to unlabeled axon terminals. sPLA2-IIA contains a strong secretory signal peptide, and it is probable that this isoform is actually secreted from neurons. In view of the effects of lysoPI on exocytosis mentioned above, it is possible that sPLA2-mediated effects on exocytosis could be partly due to the generation of lysoPI from hydrolysis of phosphatidylinositol which is located on the exofacial aspect of the cell membrane/or the inner leaflet of synaptic vesicles. It is postulated that secretion of sPLA2 from neurons and action on neuronal membranes to generate lysoPI from PI may play a role in neural transmission. If this is the case, a rapid reacylating enzyme such as lysoPI acyltransferase (Gijon et al. 2008) might also be expected to be present in CNS regions with high levels of sPLA2, and future studies are needed to evaluate this possibility. The contribution of another lysophospholipid, lysoPE to exocytosis could not be excluded, although these were not analyzed in this study due to 147 Chapter Role of lysophospholipids in synaptic transmission their insolubility in ethanol or aqueous solutions. Further work is necessary to elucidate possible sPLA2 and/or lysophospholipid mediated signaling in the CNS. 148 Section IV Conclusion SECTION IV CONCLUSION 149 Section IV Conclusion PLA2 isoforms play different roles in the CNS. Currently, there is still a lack of information regarding changes in PLA2 activity and expression after hyperalgesia and the role of PLA2 in the synaptic transmission. This study therefore, elucidated the role of PLA2, sPLA2 in particular, after orofacial pain. The changes in brain lipids indicating an increased PLA2 activity was accompanied by an increased expression of sPLA2-III. The study also demonstrated sPLA2-III function in neurotransmission using PC-12 cells. In elucidating the changes in brain lipids, it was observed that there was a decrease in phospholipids including PE and PI species, and an increase in corresponding lysophospholipids which included lysoPE, lysoPI and lysoPS in the CM after facial CA injection. These results indicated an elevated PLA2 activity and release of AA due to PLA2 enzymatic action on the phospholipids of the membrane. AA and its metabolites such as PEG2 and leukotrienes are shown to be biologically active and cause inflammation at nanomolar and micromolar concentrations (Saxena 2000; Mechiche et al. 2003; Wise 2006). These findings indicated increased CNS PLA2 activity, resulting in generation of metabolites that contribute to allodynia after peripheral inflammation. Having shown in previous studies that PLA2 inhibitors reduced nociception, the changes in expression of PLA2 isoforms including cPLA2, iPLA2, sPLA2 (sPLA2-IB, -IIA, -IIC, -IID, -IIE, -IIF, -III, -V, -X, -XIIA) were elucidated after facial CA injection. These changes likely take place in the spinal trigeminal nucleus which relays nociceptive inputs which originate from the orofacial region, and occupies a large proportion of the CM in rats. sPLA2-III mRNA expression was 150 Section V References neurotoxic phospholipase from the taipan venom. J Biol Chem 264: 11503-11510 Lambeau G, Cupillard L, Lazdunski M (1997) Membrane receptors for venom phospholipases A2. In: Kini RM (ed) Venom phospholipase A2 enzymes: structure, function and mechanism. John Wiley & Sons, Chichester, pp 389–412 Lambeau G, Lazdunski M (1999) Receptors for a growing family of secreted phospholipases A2. Trends Pharmacol Sci 20: 162-170 Lambeau G, Lazdunski M, Barhanin J (1991b) Properties of receptors for neurotoxic phospholipases A2 in different tissues. Neurochem Res 16: 651-658 Lambeau G, Schmid-Alliana A, Lazdunski M, Barhanin J (1990) Identification and purification of a very high affinity binding protein for toxic phospholipases A2 in skeletal muscle. J Biol Chem 265: 9526-9532 Lang DM, Lommel S, Jung M, Ankerhold R, Petrausch B, Laessing U, Wiechers MF, Plattner H, Stuermer CA (1998) Identification of reggie-1 and reggie-2 as plasmamembrane-associated proteins which cocluster with activated GPI-anchored cell adhesion molecules in non-caveolar micropatches in neurons. J Neurobiol 37: 502-523 Lariviere WR, Melzack R (2000) The bee venom test: comparisons with the formalin test with injection of different venoms. Pain 84: 111-112 Lariviere WR, Wilson SG, Laughlin TM, Kokayeff A, West EE, Adhikari SM, Wan Y, Mogil JS (2002) Heritability of nociception. III. Genetic relationships among commonly used assays of nociception and hypersensitivity. Pain 97: 75-86 Larsson PK, Claesson HE, Kennedy BP (1998) Multiple splice variants of the human calcium-independent phospholipase A2 and their effect on enzyme activity. J Biol Chem 273: 207-214 Lauritzen I, Heurteaux C, Lazdunski M (1994) Expression of group II phospholipase A2 in rat brain after severe forebrain ischemia and in endotoxic shock. Brain Res 651: 353-356 Lee LY, Farooqui AA, Dawe GS, Burgunder JM, Ong WY (2009) Role of phospholipase A(2) in prepulse inhibition of the auditory startle reflex in rats. Neurosci Lett 453: 6-8 Lee LY, Ong WY, Farooqui AA, Burgunder JM (2007) Role of calciumindependent phospholipase A2 in cortex striatum thalamus cortex circuitry-enzyme inhibition causes vacuous chewing movements in rats. Psychopharmacology (Berl) 195: 387-395 Lehtonen JY, Holopainen JM, Kinnunen PK (1996) Activation of phospholipase A2 by amyloid beta-peptides in vitro. Biochemistry 35: 9407-9414 Leslie CC (2004) Regulation of arachidonic acid availability for eicosanoid production. Biochem Cell Biol 82: 1-17 Leu BH, Schmidt JT (2008) Arachidonic acid as a retrograde signal controlling growth and dynamics of retinotectal arbors. Dev Neurobiol 68: 18-30 166 Section V References Lin TN, Wang Q, Simonyi A, Chen JJ, Cheung WM, He YY, Xu J, Sun AY, Hsu CY, Sun GY (2004) Induction of secretory phospholipase A2 in reactive astrocytes in response to transient focal cerebral ischemia in the rat brain. J Neurochem 90: 637-645 Liu NK, Xu XM (2010) Phospholipase A2 and its molecular mechanism after spinal cord injury. Mol Neurobiol 41: 197-205 Liu NK, Zhang YP, Han S, Pei J, Xu LY, Lu PH, Shields CB, Xu XM (2007) Annexin A1 reduces inflammatory reaction and tissue damage through inhibition of phospholipase A2 activation in adult rats following spinal cord injury. J Neuropathol Exp Neurol 66: 932-943 Liu NK, Zhang YP, Titsworth WL, Jiang X, Han S, Lu PH, Shields CB, Xu XM (2006) A novel role of phospholipase A2 in mediating spinal cord secondary injury. Ann Neurol 59: 606-619 Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25: 402-408 Lodish H BA, Kaiser CA, Krieger M, Scott MP, Bretscher A, Ploegh H, Matsudaira P (2007) Molecular cell biology. WH Freeman and Company, New York Lucas KK, Svensson CI, Hua XY, Yaksh TL, Dennis EA (2005) Spinal phospholipase A2 in inflammatory hyperalgesia: role of group IVA cPLA2. Br J Pharmacol 144: 940-952 Lukacova N, Halat G, Chavko M, Marsala J (1996) Ischemia-reperfusion injury in the spinal cord of rabbits strongly enhances lipid peroxidation and modifies phospholipid profiles. Neurochem Res 21: 869-873 Lukiw WJ, Bazan NG (2006) Survival signalling in Alzheimer's disease. Biochem Soc Trans 34: 1277-1282 Lukiw WJ, Bazan NG (2008) Docosahexaenoic acid and the aging brain. J Nutr 138: 2510-2514 Lundbaek JA, Andersen OS (1994) Lysophospholipids modulate channel function by altering the mechanical properties of lipid bilayers. J Gen Physiol 104: 645-673 Ma L, Uchida H, Nagai J, Inoue M, Aoki J, Ueda H (2010) Evidence for de novo synthesis of lysophosphatidic acid in the spinal cord through phospholipase A2 and autotaxin in nerve injury-induced neuropathic pain. J Pharmacol Exp Ther 333: 540-546 Maingret F, Patel AJ, Lesage F, Lazdunski M, Honore E (2000) Lysophospholipids open the two-pore domain mechano-gated K(+) channels TREK-1 and TRAAK. J Biol Chem 275: 10128-10133 Makela A, Sternby B, Kuusi T, Puolakkainen P, Schroder T (1990) Phospholipase A2 activity and concentration in several body fluids in patients with acute pancreatitis. Scand J Gastroenterol 25: 944-950 Martin TF (2001) PI(4,5)P(2) regulation of surface membrane traffic. Curr Opin Cell Biol 13: 493-499 167 Section V References Masuda S, Yamamoto K, Hirabayashi T, Ishikawa Y, Ishii T, Kudo I, Murakami M (2008) Human group III secreted phospholipase A2 promotes neuronal outgrowth and survival. Biochem J 409: 429-438 Matsuzawa A, Murakami M, Atsumi G, Imai K, Prados P, Inoue K, Kudo I (1996) Release of secretory phospholipase A2 from rat neuronal cells and its possible function in the regulation of catecholamine secretion. Biochem J 318 ( Pt 2): 701-709 Matthews B, Sessle BJ (2001) Peripheral mechanisms of orofacial pain. In: Lund JP, Lavigne GJ, Dubner R (eds) Orofacial pain : from basic science to clinical management ; the transfer of knowledge in pain research to education Quintessence Publishing Co, Inc, Illinois, pp 37-46 Mattson MP, Chan SL (2003) Neuronal and glial calcium signaling in Alzheimer's disease. Cell Calcium 34: 385-397 Maxfield FR, Tabas I (2005) Role of cholesterol and lipid organization in disease. Nature 438: 612-621 Mayer RJ, Marshall LA (1993) New insights on mammalian phospholipase A2(s); comparison of arachidonoyl-selective and -nonselective enzymes. FASEB J 7: 339-348 McGahon B, Clements MP, Lynch MA (1997) The ability of aged rats to sustain long-term potentiation is restored when the age-related decrease in membrane arachidonic acid concentration is reversed. Neuroscience 81: 9-16 McNeill C, Dubner R (2001) What is pain and how we classify orofacial pain? In: Lund JP, Lavigne GJ, Dubner R, Sessle BJ (eds) Orofacial pain : from basic science to clinical management ; the transfer of knowledge in pain research to education Quintessence Publishing Co, Inc, Illinois, pp 3-14 Mechiche H, Naline E, Candenas L, Pinto FM, Birembault P, Advenier C, Devillier P (2003) Effects of cysteinyl leukotrienes in small human bronchus and antagonist activity of montelukast and its metabolites. Clin Exp Allergy 33: 887-894 Merskey H, Bogduk N (1994) Classification of Chronic Pain. In: Merskey H, Bogduk N (eds). IASP Press, Seattle, pp 59-76 Metz SA (1986) Lysophosphatidylinositol, but not lysophosphatidic acid, stimulates insulin release. A possible role for phospholipase A2 but not de novo synthesis of lysophospholipid in pancreatic islet function. Biochem Biophys Res Commun 138: 720-727 Meves H (2008) Arachidonic acid and ion channels: an update. Br J Pharmacol 155: 4-16 Millanvoye-Van Brussel E, Topal G, Brunet A, Do Pham T, Deckert V, Rendu F, David-Dufilho M (2004) Lysophosphatidylcholine and 7-oxocholesterol modulate Ca2+ signals and inhibit the phosphorylation of endothelial NO synthase and cytosolic phospholipase A2. Biochem J 380: 533-539 Mogil JS, Wilson SG, Bon K, Lee SE, Chung K, Raber P, Pieper JO, Hain HS, Belknap JK, Hubert L, Elmer GI, Chung JM, Devor M (1999) Heritability of 168 Section V References nociception I: responses of 11 inbred mouse strains on 12 measures of nociception. Pain 80: 67-82 Molloy GY, Rattray M, Williams RJ (1998) Genes encoding multiple forms of phospholipase A2 are expressed in rat brain. Neurosci Lett 258: 139-142 Moolenaar WH (1999) Bioactive lysophospholipids and their G protein-coupled receptors. Exp Cell Res 253: 230-238 Moolenaar WH, van Meeteren LA, Giepmans BN (2004) The ins and outs of lysophosphatidic acid signaling. Bioessays 26: 870-881 Morgan NV, Westaway SK, Morton JE, Gregory A, Gissen P, Sonek S, Cangul H, Coryell J, Canham N, Nardocci N, Zorzi G, Pasha S, Rodriguez D, Desguerre I, Mubaidin A, Bertini E, Trembath RC, Simonati A, Schanen C, Johnson CA, Levinson B, Woods CG, Wilmot B, Kramer P, Gitschier J, Maher ER, Hayflick SJ (2006) PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron. Nat Genet 38: 752-754 Morioka N, Takeda K, Kumagai K, Hanada T, Ikoma K, Hide I, Inoue A, Nakata Y (2002) Interleukin-1beta-induced substance P release from rat cultured primary afferent neurons driven by two phospholipase A2 enzymes: secretory type IIA and cytosolic type IV. J Neurochem 80: 989-997 Morioka Y, Ikeda M, Saiga A, Fujii N, Ishimoto Y, Arita H, Hanasaki K (2000a) Potential role of group X secretory phospholipase A(2) in cyclooxygenase2-dependent PGE(2) formation during colon tumorigenesis. FEBS Lett 487: 262-266 Morioka Y, Saiga A, Yokota Y, Suzuki N, Ikeda M, Ono T, Nakano K, Fujii N, Ishizaki J, Arita H, Hanasaki K (2000b) Mouse group X secretory phospholipase A2 induces a potent release of arachidonic acid from spleen cells and acts as a ligand for the phospholipase A2 receptor. Arch Biochem Biophys 381: 31-42 Moses GS, Jensen MD, Lue LF, Walker DG, Sun AY, Simonyi A, Sun GY (2006) Secretory PLA2-IIA: a new inflammatory factor for Alzheimer's disease. J Neuroinflammation 3: 28 Moskowitz N, Puszkin S, Schook W (1983) Characterization of brain synaptic vesicle phospholipase A2 activity and its modulation by calmodulin, prostaglandin E2, prostaglandin F2 alpha, cyclic AMP, and ATP. J Neurochem 41: 1576-1586 Moskowitz N, Spiera H, Lahita RG, Puszkin S (1986) Brain protein kinase in synaptic vesicles is inhibited by a factor in sera from systemic lupus erythematosus patients with central nervous system manifestations. Brain Res 370: 38-43 Mounier CM, Wendum D, Greenspan E, Flejou JF, Rosenberg DW, Lambeau G (2008) Distinct expression pattern of the full set of secreted phospholipases A2 in human colorectal adenocarcinomas: sPLA2-III as a biomarker candidate. Br J Cancer 98: 587-595 Murakami M, Kambe T, Shimbara S, Higashino K, Hanasaki K, Arita H, Horiguchi M, Arita M, Arai H, Inoue K, Kudo I (1999) Different functional aspects of 169 Section V References the group II subfamily (Types IIA and V) and type X secretory phospholipase A(2)s in regulating arachidonic acid release and prostaglandin generation. Implications of cyclooxygenase-2 induction and phospholipid scramblase-mediated cellular membrane perturbation. J Biol Chem 274: 31435-31444 Murakami M, Kudo I (2001) Diversity and regulatory functions of mammalian secretory phospholipase A2s. Adv Immunol 77: 163-194 Murakami M, Kudo I (2002) Phospholipase A2. J Biochem 131: 285-292 Murakami M, Kudo I (2004) Secretory phospholipase A2. Biol Pharm Bull 27: 1158-1164 Murakami M, Kudo I, Inoue K (1995) Secretory phospholipases A2. J Lipid Mediat Cell Signal 12: 119-130 Murakami M, Kudo I, Nakamura H, Yokoyama Y, Mori H, Inoue K (1990) Exacerbation of rat adjuvant arthritis by intradermal injection of purified mammalian 14-kDa group II phospholipase A2. FEBS Lett 268: 113-116 Murakami M, Masuda S, Shimbara S, Bezzine S, Lazdunski M, Lambeau G, Gelb MH, Matsukura S, Kokubu F, Adachi M, Kudo I (2003) Cellular arachidonate-releasing function of novel classes of secretory phospholipase A2s (groups III and XII). J Biol Chem 278: 10657-10667 Murakami M, Masuda S, Shimbara S, Ishikawa Y, Ishii T, Kudo I (2005) Cellular distribution, post-translational modification, and tumorigenic potential of human group III secreted phospholipase A(2). J Biol Chem 280: 2498724998 Murakami M, Nakatani Y, Atsumi G, Inoue K, Kudo I (1997) Regulatory functions of phospholipase A2. Crit Rev Immunol 17: 225-283 Murakami M, Shimbara S, Kambe T, Kuwata H, Winstead MV, Tischfield JA, Kudo I (1998) The functions of five distinct mammalian phospholipase A2S in regulating arachidonic acid release. Type IIa and type V secretory phospholipase A2S are functionally redundant and act in concert with cytosolic phospholipase A2. J Biol Chem 273: 14411-14423 Murphy EJ, Behrmann D, Bates CM, Horrocks LA (1994) Lipid alterations following impact spinal cord injury in the rat. Mol Chem Neuropathol 23: 13-26 Nakano T, Ohara O, Teraoka H, Arita H (1990) Glucocorticoids suppress group II phospholipase A2 production by blocking mRNA synthesis and posttranscriptional expression. J Biol Chem 265: 12745-12748 Nakashima S, Ikeno Y, Yokoyama T, Kuwana M, Bolchi A, Ottonello S, Kitamoto K, Arioka M (2003) Secretory phospholipases A2 induce neurite outgrowth in PC12 cells. Biochem J 376: 655-666 Nanda BL, Nataraju A, Rajesh R, Rangappa KS, Shekar MA, Vishwanath BS (2007) PLA2 mediated arachidonate free radicals: PLA2 inhibition and neutralization of free radicals by anti-oxidants--a new role as antiinflammatory molecule. Curr Top Med Chem 7: 765-777 Naraba H, Murakami M, Matsumoto H, Shimbara S, Ueno A, Kudo I, Oh-ishi S (1998) Segregated coupling of phospholipases A2, cyclooxygenases, and 170 Section V References terminal prostanoid synthases in different phases of prostanoid biosynthesis in rat peritoneal macrophages. J Immunol 160: 2974-2982 Nathan RD, Kanai K, Clark RB, Giles W (1988) Selective block of calcium current by lanthanum in single bullfrog atrial cells. J Gen Physiol 91: 549-572 Nevalainen TJ, Haapamaki MM, Gronroos JM (2000) Roles of secretory phospholipases A(2) in inflammatory diseases and trauma. Biochim Biophys Acta 1488: 83-90 Ng CH, Ong WY (2001) Increased expression of gamma-aminobutyric acid transporters GAT-1 and GAT-3 in the spinal trigeminal nucleus after facial carrageenan injections. Pain 92: 29-40 Nicolas JP, Lin Y, Lambeau G, Ghomashchi F, Lazdunski M, Gelb MH (1997) Localization of structural elements of bee venom phospholipase A2 involved in N-type receptor binding and neurotoxicity. J Biol Chem 272: 7173-7181 Nicolau DV, Jr., Burrage K, Parton RG, Hancock JF (2006) Identifying optimal lipid raft characteristics required to promote nanoscale protein-protein interactions on the plasma membrane. Mol Cell Biol 26: 313-323 Nieva JL, Goni FM, Alonso A (1989) Liposome fusion catalytically induced by phospholipase C. Biochemistry 28: 7364-7367 Nomura T, Nishizaki T, Enomoto T, Itoh H (2001) A long-lasting facilitation of hippocampal neurotransmission via a phospholipase A2 signaling pathway. Life Sci 68: 2885-2891 Nyman KM, Ojala P, Laine VJ, Nevalainen TJ (2000) Distribution of group II phospholipase A2 protein and mRNA in rat tissues. J Histochem Cytochem 48: 1469-1478 O'Regan MH, Alix S, Woodbury DJ (1996) Phospholipase A2-evoked destabilization of planar lipid membranes. Neurosci Lett 202: 201-203 O'Regan MH, Perkins LM, Phillis JW (1995a) Arachidonic acid and lysophosphatidylcholine modulate excitatory transmitter amino acid release from the rat cerebral cortex. Neurosci Lett 193: 85-88 O'Regan MH, Smith-Barbour M, Perkins LM, Phillis JW (1995b) A possible role for phospholipases in the release of neurotransmitter amino acids from ischemic rat cerebral cortex. Neurosci Lett 185: 191-194 Oka S, Arita H (1991) Inflammatory factors stimulate expression of group II phospholipase A2 in rat cultured astrocytes. Two distinct pathways of the gene expression. J Biol Chem 266: 9956-9960 Oliveira AC, Bertollo CM, Rocha LT, Nascimento EB, Jr., Costa KA, Coelho MM (2007) Antinociceptive and antiedematogenic activities of fenofibrate, an agonist of PPAR alpha, and pioglitazone, an agonist of PPAR gamma. Eur J Pharmacol 561: 194-201 Ong WY, Farooqui T, Farooqui AA (2010) Involvement of cytosolic phospholipase A(2), calcium independent phospholipase A(2) and plasmalogen selective phospholipase A(2) in neurodegenerative and neuropsychiatric conditions. Curr Med Chem 17: 2746-2763 171 Section V References Ong WY, Horrocks LA, Farooqui AA (1999a) Immunocytochemical localization of cPLA2 in rat and monkey spinal cord. J Mol Neurosci 12: 123-130 Ong WY, Sandhya TL, Horrocks LA, Farooqui AA (1999b) Distribution of cytoplasmic phospholipase A2 in the normal rat brain. J Hirnforsch 39: 391-400 Ong WY, Yeo JF, Ling SF, Farooqui AA (2005) Distribution of calciumindependent phospholipase A2 (iPLA 2) in monkey brain. J Neurocytol 34: 447-458 Ono T, Tojo H, Kuramitsu S, Kagamiyama H, Okamoto M (1988) Purification and characterization of a membrane-associated phospholipase A2 from rat spleen. Its comparison with a cytosolic phospholipase A2 S-1. J Biol Chem 263: 5732-5738 Orr JW, Newton AC (1992) Interaction of protein kinase C with phosphatidylserine. 1. Cooperativity in lipid binding. Biochemistry 31: 4661-4667 Orr SK, Bazinet RP (2008) The emerging role of docosahexaenoic acid in neuroinflammation. Curr Opin Investig Drugs 9: 735-743 Pal S, Sombati S, Limbrick DD, Jr., DeLorenzo RJ (1999) In vitro status epilepticus causes sustained elevation of intracellular calcium levels in hippocampal neurons. Brain Res 851: 20-31 Pan CY, Lee H, Chen CL (2006) Lysophospholipids elevate [Ca2+]i and trigger exocytosis in bovine chromaffin cells. Neuropharmacology 51: 18-26 Patrick CB, Krzywkowski P, Ramassamy C, Poirier J, Rapoport SI, Murphy EJ (2000) Phospholipase A2 activity is decreased selectively in the hippocampus of aged apolipoprotein E deficient mice. Neurosci Lett 288: 211-214 Phillis JW, O'Regan MH (2004) A potentially critical role of phospholipases in central nervous system ischemic, traumatic, and neurodegenerative disorders. Brain Res Brain Res Rev 44: 13-47 Pinto F, Brenner T, Dan P, Krimsky M, Yedgar S (2003) Extracellular phospholipase A2 inhibitors suppress central nervous system inflammation. Glia 44: 275-282 Piomelli D, Astarita G, Rapaka R (2007) A neuroscientist's guide to lipidomics. Nat Rev Neurosci 8: 743-754 Poh KW, Lutfun N, Manikandan J, Ong WY, Yeo JF (2009) Global gene expression analysis in the mouse brainstem after hyperalgesia induced by facial carrageenan injection--evidence for a form of neurovascular coupling? Pain 142: 133-141 Popoli M, Venegoni A, Buffa L, Racagni G (1997) Ca2+/phospholipid-binding and syntaxin-binding of native synaptotagmin I. Life Sci 61: 711-721 Pruzanski W, Bogoch E, Wloch M, Vadas P (1991) The role of phospholipase A2 in the physiopathology of osteoarthritis. J Rheumatol Suppl 27: 117-119 Pruzanski W, Lin KS, Vadas P (1995) Secretory phospholipase A2 in rheumatic diseases In: Glacer KB, Vadas P (eds) Phospholipase A2 in clinical inflammation. CRC Press, Boca Raton, pp 127-147 172 Section V References Quetglas S, Iborra C, Sasakawa N, De Haro L, Kumakura K, Sato K, Leveque C, Seagar M (2002) Calmodulin and lipid binding to synaptobrevin regulates calcium-dependent exocytosis. EMBO J 21: 3970-3979 Raichel L, Berger S, Hadad N, Kachko L, Karter M, Szaingurten-Solodkin I, Williams RO, Feldmann M, Levy R (2008) Reduction of cPLA2alpha overexpression: an efficient anti-inflammatory therapy for collageninduced arthritis. Eur J Immunol 38: 2905-2915 Ramanadham S, Hsu FF, Bohrer A, Ma Z, Turk J (1999) Studies of the role of group VI phospholipase A2 in fatty acid incorporation, phospholipid remodeling, lysophosphatidylcholine generation, and secretagogueinduced arachidonic acid release in pancreatic islets and insulinoma cells. J Biol Chem 274: 13915-13927 Rao JS, Ertley RN, Lee HJ, DeMar JC, Jr., Arnold JT, Rapoport SI, Bazinet RP (2007) n-3 polyunsaturated fatty acid deprivation in rats decreases frontal cortex BDNF via a p38 MAPK-dependent mechanism. Mol Psychiatry 12: 36-46 Rastogi P, McHowat J (2009) Inhibition of calcium-independent phospholipase A2 prevents inflammatory mediator production in pulmonary microvascular endothelium. Respir Physiol Neurobiol 165: 167-174 Rausell E, Jones EG (1991) Chemically distinct compartments of the thalamic VPM nucleus in monkeys relay principal and spinal trigeminal pathways to different layers of the somatosensory cortex. J Neurosci 11: 226-237 Ray P, Millard CB, Petrali JP, Berman JD, Ray R (1997) Acetylcholine exocytosis in PC12 cells deficient in SNAP-25. Neuroreport 8: 2271-2274 Raza M, Pal S, Rafiq A, DeLorenzo RJ (2001) Long-term alteration of calcium homeostatic mechanisms in the pilocarpine model of temporal lobe epilepsy. Brain Res 903: 1-12 Resnick DK, Nguyen P, Cechvala CF (2001) Regional and temporal changes in prostaglandin E2 and thromboxane B2 concentrations after spinal cord injury. Spine J 1: 432-436 Rigoni M, Caccin P, Gschmeissner S, Koster G, Postle AD, Rossetto O, Schiavo G, Montecucco C (2005) Equivalent effects of snake PLA2 neurotoxins and lysophospholipid-fatty acid mixtures. Science 310: 1678-1680 Rodriguez De Turco EB, Jackson FR, DeCoster MA, Kolko M, Bazan NG (2002) Glutamate signalling and secretory phospholipase A2 modulate the release of arachidonic acid from neuronal membranes. J Neurosci Res 68: 558-567 Roshak A, Sathe G, Marshall LA (1994) Suppression of monocyte 85-kDa phospholipase A2 by antisense and effects on endotoxin-induced prostaglandin biosynthesis. J Biol Chem 269: 25999-26005 Rossi V, Leoncini S, Signorini C, Buonocore G, Paffetti P, Tanganelli D, Ciccoli L, Comporti M (2006) Oxidative stress and autologous immunoglobulin G binding to band dimers in newborn erythrocytes. Free Radic Biol Med 40: 907-915 173 Section V References Rubin RP, Thompson RH, Laychock SG (1990) Characterization of phospholipase A2 and acyltransferase activities in purified zymogen granule membranes. Biochim Biophys Acta 1045: 245-251 Ryberg E, Larsson N, Sjogren S, Hjorth S, Hermansson NO, Leonova J, Elebring T, Nilsson K, Drmota T, Greasley PJ (2007) The orphan receptor GPR55 is a novel cannabinoid receptor. Br J Pharmacol 152: 1092-1101 Samad TA, Moore KA, Sapirstein A, Billet S, Allchorne A, Poole S, Bonventre JV, Woolf CJ (2001) Interleukin-1beta-mediated induction of Cox-2 in the CNS contributes to inflammatory pain hypersensitivity. Nature 410: 471-475 Sandhya TL, Ong WY, Horrocks LA, Farooqui AA (1998) A light and electron microscopic study of cytoplasmic phospholipase A2 and cyclooxygenase2 in the hippocampus after kainate lesions. Brain Res 788: 223-231 Sato H, Kato R, Isogai Y, Saka G, Ohtsuki M, Taketomi Y, Yamamoto K, Tsutsumi K, Yamada J, Masuda S, Ishikawa Y, Ishii T, Kobayashi T, Ikeda K, Taguchi R, Hatakeyama S, Hara S, Kudo I, Itabe H, Murakami M (2008) Analyses of group III secreted phospholipase A2 transgenic mice reveal potential participation of this enzyme in plasma lipoprotein modification, macrophage foam cell formation, and atherosclerosis. J Biol Chem 283: 33483-33497 Sato H, Taketomi Y, Isogai Y, Masuda S, Kobayashi T, Yamamoto K, Murakami M (2009) Group III secreted phospholipase A2 transgenic mice spontaneously develop inflammation. Biochem J 421: 17-27 Sawada H, Murakami M, Enomoto A, Shimbara S, Kudo I (1999) Regulation of type V phospholipase A2 expression and function by proinflammatory stimuli. Eur J Biochem 263: 826-835 Sawzdargo M, Nguyen T, Lee DK, Lynch KR, Cheng R, Heng HH, George SR, O'Dowd BF (1999) Identification and cloning of three novel human G protein-coupled receptor genes GPR52, PsiGPR53 and GPR55: GPR55 is extensively expressed in human brain. Brain Res Mol Brain Res 64: 193198 Saxena NC (2000) Inhibition of GABA(A) receptor (GABAR) currents by arachidonic acid in HEK 293 cells stably transfected with alpha1beta2gamma2 GABAR subunits. Pflugers Arch 440: 380-392 Schaefers HJ, Haselmann J, Goppelt-Struebe M (1996) Regulation of prostaglandin synthesis in Madin Darby canine kidney cells: role of prostaglandin G/H synthase and secreted phospholipase A2. Biochim Biophys Acta 1300: 197-202 Schaloske RH, Dennis EA (2006) The phospholipase A2 superfamily and its group numbering system. Biochim Biophys Acta 1761: 1246-1259 Schroeder TJ, Jankowski JA, Kawagoe KT, Wightman RM, Lefrou C, Amatore C (1992) Analysis of diffusional broadening of vesicular packets of catecholamines released from biological cells during exocytosis. Anal Chem 64: 3077-3083 Schwab JM, Chiang N, Arita M, Serhan CN (2007) Resolvin E1 and protectin D1 activate inflammation-resolution programmes. Nature 447: 869-874 174 Section V References Scott DL, Otwinowski Z, Gelb MH, Sigler PB (1991) Crystal structure of beevenom phospholipase A2: correction. Science 252: 764 Seibert K, Zhang Y, Leahy K, Hauser S, Masferrer J, Perkins W, Lee L, Isakson P (1994) Pharmacological and biochemical demonstration of the role of cyclooxygenase in inflammation and pain. Proc Natl Acad Sci U S A 91: 12013-12017 Seilhamer JJ, Pruzanski W, Vadas P, Plant S, Miller JA, Kloss J, Johnson LK (1989) Cloning and recombinant expression of phospholipase A2 present in rheumatoid arthritic synovial fluid. J Biol Chem 264: 5335-5338 Seleznev K, Zhao C, Zhang XH, Song K, Ma ZA (2006) Calcium-independent phospholipase A2 localizes in and protects mitochondria during apoptotic induction by staurosporine. J Biol Chem 281: 22275-22288 Senisterra G, Epand RM (1993) Role of membrane defects in the regulation of the activity of protein kinase C. Arch Biochem Biophys 300: 378-383 Sessle BJ (2000) Acute and chronic craniofacial pain: brainstem mechanisms of nociceptive transmission and neuroplasticity, and their clinical correlates. Crit Rev Oral Biol Med 11: 57-91 Sessle BJ (2005) Peripheral and central mechanisms of orofacial pain and their clinical correlates. Minerva Anestesiol 71: 117-136 Seybold VS, Jia YP, Abrahams LG (2003) Cyclo-oxygenase-2 contributes to central sensitization in rats with peripheral inflammation. Pain 105: 47-55 Sharir H, Abood ME (2010) Pharmacological characterization of GPR55, a putative cannabinoid receptor. Pharmacol Ther 126: 301-313 Shen AY, Huang MH, Wang TS, Wu HM, Kang YF, Chen CL (2009) Thymolevoked Ca+ mobilization and ion currents in pituitary GH3 cells. Nat Prod Commun 4: 749-752 Sherman SE, Luo L, Dostrovsky JO (1997) Spinal strychnine alters response properties of nociceptive-specific neurons in rat medial thalamus. J Neurophysiol 78: 628-637 Shiono S, Kawamoto K, Yoshida N, Kondo T, Inagami T (1993) Neurotransmitter release from lysophosphatidic acid stimulated PC12 cells: involvement of lysophosphatidic acid receptors. Biochem Biophys Res Commun 193: 667-673 Shirai Y, Ito M (2004) Specific differential expression of phospholipase A2 subtypes in rat cerebellum. J Neurocytol 33: 297-307 Shui G, Bendt AK, Pethe K, Dick T, Wenk MR (2007) Sensitive profiling of chemically diverse bioactive lipids. J Lipid Res 48: 1976-1984 Shvartsman DE, Gutman O, Tietz A, Henis YI (2006) Cyclodextrins but not compactin inhibit the lateral diffusion of membrane proteins independent of cholesterol. Traffic 7: 917-926 Simons K, Toomre D (2000) Lipid rafts and signal transduction. Nat Rev Mol Cell Biol 1: 31-39 Singaravelu K, Lohr C, Deitmer JW (2008) Calcium-independent phospholipase A2 mediates store-operated calcium entry in rat cerebellar granule cells. Cerebellum 7: 467-481 175 Section V References Siqueira RS, Bonjardim LR, Araujo AA, Araujo BE, Melo MG, Oliveira MG, Gelain DP, Silva FA, DeSantana JM, Albuquerque-Junior RL, Rocha RF, Moreira JC, Antoniolli AR, Quintans-Junior LJ (2010) Antinociceptive activity of atranorin in mice orofacial nociception tests. Z Naturforsch C 65: 551-561 Six DA, Barbayianni E, Loukas V, Constantinou-Kokotou V, Hadjipavlou-Litina D, Stephens D, Wong AC, Magrioti V, Moutevelis-Minakakis P, Baker SF, Dennis EA, Kokotos G (2007) Structure-activity relationship of 2-oxoamide inhibition of group IVA cytosolic phospholipase A2 and group V secreted phospholipase A2. J Med Chem 50: 4222-4235 Six DA, Dennis EA (2000) The expanding superfamily of phospholipase A(2) enzymes: classification and characterization. Biochim Biophys Acta 1488: 1-19 Smalheiser NR, Swanson DR (1998) Calcium-independent phospholipase A2 and schizophrenia. Arch Gen Psychiatry 55: 752-753 Smith GA, Hesketh TR, Plumb RW, Metcalfe JC (1979) The exogenous lipid requirement for histamine release from rat peritoneal mast cells stimulated by concanavalin A. FEBS Lett 105: 58-62 Snitko Y, Han SK, Lee BI, Cho W (1999) Differential interfacial and substrate binding modes of mammalian pancreatic phospholipases A2: a comparison among human, bovine, and porcine enzymes. Biochemistry 38: 7803-7810 Stiles MA, Mitrirattanakul S, Evans JJ (2007), Clinical Manual of Trigeminal Neuralgia, Informa Healthcare, UK, p36. Strokin M, Chechneva O, Reymann KG, Reiser G (2006) Neuroprotection of rat hippocampal slices exposed to oxygen-glucose deprivation by enrichment with docosahexaenoic acid and by inhibition of hydrolysis of docosahexaenoic acid-containing phospholipids by calcium independent phospholipase A2. Neuroscience 140: 547-553 Strokin M, Sergeeva M, Reiser G (2007) Prostaglandin synthesis in rat brain astrocytes is under the control of the n-3 docosahexaenoic acid, released by group VIB calcium-independent phospholipase A2. J Neurochem 102: 1771-1782 Sugo T, Tachimoto H, Chikatsu T, Murakami Y, Kikukawa Y, Sato S, Kikuchi K, Nagi T, Harada M, Ogi K, Ebisawa M, Mori M (2006) Identification of a lysophosphatidylserine receptor on mast cells. Biochem Biophys Res Commun 341: 1078-1087 Sun GY, Horrocks LA, Farooqui AA (2007) The roles of NADPH oxidase and phospholipases A2 in oxidative and inflammatory responses in neurodegenerative diseases. J Neurochem 103: 1-16 Sun GY, MacQuarrie RA (1989) Deacylation-reacylation of arachidonoyl groups in cerebral phospholipids. Ann N Y Acad Sci 559: 37-55 Sun GY, Shelat PB, Jensen MB, He Y, Sun AY, Simonyi A (2010) Phospholipases A2 and inflammatory responses in the central nervous system. Neuromolecular Med 12: 133-148 176 Section V References Sun GY, Xu J, Jensen MD, Simonyi A (2004) Phospholipase A2 in the central nervous system: implications for neurodegenerative diseases. J Lipid Res 45: 205-213 Sun JY, Wu LG (2001) Fast kinetics of exocytosis revealed by simultaneous measurements of presynaptic capacitance and postsynaptic currents at a central synapse. Neuron 30: 171-182 Sun ZX, Zhou QH, Sui SF (2005) Cholesterol depletion inhibits the degradation of amyloid beta-peptide in rat pheochromocytoma (PC12) cells. Neurosci Lett 391: 71-75 Sundstrom E, Mo LL (2002) Mechanisms of glutamate release in the rat spinal cord slices during metabolic inhibition. J Neurotrauma 19: 257-266 Suvinen TI, Reade PC, Kemppainen P, Kononen M, Dworkin SF (2005) Review of aetiological concepts of temporomandibular pain disorders: towards a biopsychosocial model for integration of physical disorder factors with psychological and psychosocial illness impact factors. Eur J Pain 9: 613633 Suzuki N, Ishizaki J, Yokota Y, Higashino K, Ono T, Ikeda M, Fujii N, Kawamoto K, Hanasaki K (2000) Structures, enzymatic properties, and expression of novel human and mouse secretory phospholipase A(2)s. J Biol Chem 275: 5785-5793 Svensson CI, Lucas KK, Hua XY, Powell HC, Dennis EA, Yaksh TL (2005) Spinal phospholipase A2 in inflammatory hyperalgesia: role of the small, secretory phospholipase A2. Neuroscience 133: 543-553 Svensson CI, Yaksh TL (2002) The spinal phospholipase-cyclooxygenaseprostanoid cascade in nociceptive processing. Annu Rev Pharmacol Toxicol 42: 553-583 Tachikawa M, Tsuji K, Ikeda S, Hosoya K (2009) Lysophospholipids enhance taurine release from rat retinal vascular endothelial cells under hypoosmotic stress. Microvasc Res 78: 332-337 Takemura M, Sugiyo S, Moritani M, Kobayashi M, Yonehara N (2006) Mechanisms of orofacial pain control in the central nervous system. Arch Histol Cytol 69: 79-100 Tanaka M, Cummins TR, Ishikawa K, Dib-Hajj SD, Black JA, Waxman SG (1998) SNS Na+ channel expression increases in dorsal root ganglion neurons in the carrageenan inflammatory pain model. Neuroreport 9: 967-972 Tang N, Ong WY, Zhang EM, Chen P, Yeo JF (2007) Differential effects of ceramide species on exocytosis in rat PC12 cells. Exp Brain Res 183: 241-247 Telleria-Diaz A, Schmidt M, Kreusch S, Neubert AK, Schache F, Vazquez E, Vanegas H, Schaible HG, Ebersberger A (2010) Spinal antinociceptive effects of cyclooxygenase inhibition during inflammation: Involvement of prostaglandins and endocannabinoids. Pain 148: 26-35 Than A, Tan Y, Ong WY, Farooqui AA, Chen P (2011) Kainate receptors mediate regulated secretion and exocytosis of secretory phospholipase A2 in SHSY5Y neuroblastoma cells. 177 Section V References Thwin MM, Ong WY, Fong CW, Sato K, Kodama K, Farooqui AA, Gopalakrishnakone P (2003) Secretory phospholipase A2 activity in the normal and kainate injected rat brain, and inhibition by a peptide derived from python serum. Exp Brain Res 150: 427-433 Tischfield JA (1997) A reassessment of the low molecular weight phospholipase A2 gene family in mammals. J Biol Chem 272: 17247-17250 Titsworth WL, Cheng X, Ke Y, Deng L, Burckardt KA, Pendleton C, Liu NK, Shao H, Cao QL, Xu XM (2009) Differential expression of sPLA2 following spinal cord injury and a functional role for sPLA2-IIA in mediating oligodendrocyte death. Glia 57: 1521-1537 Titsworth WL, Liu NK, Xu XM (2008) Role of secretory phospholipase a(2) in CNS inflammation: implications in traumatic spinal cord injury. CNS Neurol Disord Drug Targets 7: 254-269 Titsworth WL, Onifer SM, Liu NK, Xu XM (2007) Focal phospholipases A2 group III injections induce cervical white matter injury and functional deficits with delayed recovery concomitant with Schwann cell remyelination. Exp Neurol 207: 150-162 Tonai T, Taketani Y, Ueda N, Nishisho T, Ohmoto Y, Sakata Y, Muraguchi M, Wada K, Yamamoto S (1999) Possible involvement of interleukin-1 in cyclooxygenase-2 induction after spinal cord injury in rats. J Neurochem 72: 302-309 Trushina E, Du Charme J, Parisi J, McMurray CT (2006) Neurological abnormalities in caveolin-1 knock out mice. Behav Brain Res 172: 24-32 Uchiyama Y, Maxson MM, Sawada T, Nakano A, Ewing AG (2007) Phospholipid mediated plasticity in exocytosis observed in PC12 cells. Brain Res 1151: 46-54 Vadas P, Pruzanski W (1984) Role of extracellular phospholipase A2 in inflammation. Adv Inflamm Res: 52-59 Vadas P, Pruzanski W, Kim J, Fornasier V (1989) The proinflammatory effect of intra-articular injection of soluble human and venom phospholipase A2. Am J Pathol 134: 807-811 Vahidy WH, Ong WY, Farooqui AA, Yeo JF (2006) Effects of intracerebroventricular injections of free fatty acids, lysophospholipids, or platelet activating factor in a mouse model of orofacial pain. Exp Brain Res 174: 781-785 Valentin E, Ghomashchi F, Gelb MH, Lazdunski M, Lambeau G (1999a) On the diversity of secreted phospholipases A(2). Cloning, tissue distribution, and functional expression of two novel mouse group II enzymes. J Biol Chem 274: 31195-31202 Valentin E, Ghomashchi F, Gelb MH, Lazdunski M, Lambeau G (2000) Novel human secreted phospholipase A(2) with homology to the group III bee venom enzyme. J Biol Chem 275: 7492-7496 Valentin E, Koduri RS, Scimeca JC, Carle G, Gelb MH, Lazdunski M, Lambeau G (1999b) Cloning and recombinant expression of a novel mousesecreted phospholipase A2. J Biol Chem 274: 19152-19160 178 Section V References Valentin E, Lambeau G (2000) Increasing molecular diversity of secreted phospholipases A(2) and their receptors and binding proteins. Biochim Biophys Acta 1488: 59-70 Valtorta F, Meldolesi J (1994) The presynaptic compartment: signals and targets. Semin Cell Biol 5: 211-219 Volterra A, Trotti D, Racagni G (1994) Glutamate uptake is inhibited by arachidonic acid and oxygen radicals via two distinct and additive mechanisms. Mol Pharmacol 46: 986-992 Vos BP, Strassman AM, Maciewicz RJ (1994) Behavioral evidence of trigeminal neuropathic pain following chronic constriction injury to the rat's infraorbital nerve. J Neurosci 14: 2708-2723 Walker HK (1990) Cranial Nerve V: The Trigeminal Nerve. Wang G, Zhou D, Wang C, Gao Y, Zhou Q, Qian G, DeCoster MA (2010) Hypoxic preconditioning suppresses group III secreted phospholipase A2induced apoptosis via JAK2-STAT3 activation in cortical neurons. J Neurochem 114: 1039-1048 Watson AD (2006) Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res 47: 2101-2111 Wei S, Ong WY, Thwin MM, Fong CW, Farooqui AA, Gopalakrishnakone P, Hong W (2003) Group IIA secretory phospholipase A2 stimulates exocytosis and neurotransmitter release in pheochromocytoma-12 cells and cultured rat hippocampal neurons. Neuroscience 121: 891-898 Weltzien HU (1979) Cytolytic and membrane-perturbing properties of lysophosphatidylcholine. Biochim Biophys Acta 559: 259-287 Wenk MR (2005) The emerging field of lipidomics. Nat Rev Drug Discov 4: 594610 Wenk MR, De Camilli P (2004) Protein-lipid interactions and phosphoinositide metabolism in membrane traffic: insights from vesicle recycling in nerve terminals. Proc Natl Acad Sci U S A 101: 8262-8269 Wheeler-Aceto H, Porreca F, Cowan A (1990) The rat paw formalin test: comparison of noxious agents. Pain 40: 229-238 Williams MN, Zahm DS, Jacquin MF (1994) Differential foci and synaptic organization of the principal and spinal trigeminal projections to the thalamus in the rat. Eur J Neurosci 6: 429-453 Wise H (2006) Lack of interaction between prostaglandin E2 receptor subtypes in regulating adenylyl cyclase activity in cultured rat dorsal root ganglion cells. Eur J Pharmacol 535: 69-77 Wolfe LS, Horrocks LA (1994) Eicosanoids. In: Siegel GJ, Agranoff BW, Albers RW, Molinoff PB (eds) Basic Neurochemistry. Raven Press, New York, pp 475-490 Won JS, Im YB, Khan M, Singh AK, Singh I (2005) Involvement of phospholipase A2 and lipoxygenase in lipopolysaccharide-induced inducible nitric oxide synthase expression in glial cells. Glia 51: 13-21 179 Section V References Xu J, Chalimoniuk M, Shu Y, Simonyi A, Sun AY, Gonzalez FA, Weisman GA, Wood WG, Sun GY (2003a) Prostaglandin E2 production in astrocytes: regulation by cytokines, extracellular ATP, and oxidative agents. Prostaglandins Leukot Essent Fatty Acids 69: 437-448 Xu J, Yu S, Sun AY, Sun GY (2003b) Oxidant-mediated AA release from astrocytes involves cPLA(2) and iPLA(2). Free Radic Biol Med 34: 15311543 Yagami T, Ueda K, Asakura K, Hata S, Kuroda T, Sakaeda T, Takasu N, Tanaka K, Gemba T, Hori Y (2002) Human group IIA secretory phospholipase A2 induces neuronal cell death via apoptosis. Mol Pharmacol 61: 114-126 Yagami T, Ueda K, Asakura K, Nakazato H, Hata S, Kuroda T, Sakaeda T, Sakaguchi G, Itoh N, Hashimoto Y, Hori Y (2003a) Human group IIA secretory phospholipase A2 potentiates Ca2+ influx through L-type voltage-sensitive Ca2+ channels in cultured rat cortical neurons. J Neurochem 85: 749-758 Yagami T, Ueda K, Asakura K, Okamura N, Sakaeda T, Sakaguchi G, Itoh N, Hashimoto Y, Nakano T, Fujimoto M (2003b) Effect of Gas6 on secretory phospholipase A(2)-IIA-induced apoptosis in cortical neurons. Brain Res 985: 142-149 Yamashita A, Sugiura T, Waku K (1997) Acyltransferases and transacylases involved in fatty acid remodeling of phospholipids and metabolism of bioactive lipids in mammalian cells. J Biochem 122: 1-16 Yang CS, Yuk JM, Shin DM, Kang J, Lee SJ, Jo EK (2009) Secretory phospholipase A2 plays an essential role in microglial inflammatory responses to Mycobacterium tuberculosis. Glia 57: 1091-1103 Yang X, Sheng W, He Y, Cui J, Haidekker MA, Sun GY, Lee JC (2010) Secretory phospholipase A2 type III enhances alpha-secretase-dependent amyloid precursor protein processing through alterations in membrane fluidity. J Lipid Res 51: 957-966 Yeo JF, Ong WY, Ling SF, Farooqui AA (2004) Intracerebroventricular injection of phospholipases A2 inhibitors modulates allodynia after facial carrageenan injection in mice. Pain 112: 148-155 You HJ, Colpaert FC, Arendt-Nielsen L (2008) Long-lasting descending and transitory short-term spinal controls on deep spinal dorsal horn nociceptive-specific neurons in response to persistent nociception. Brain Res Bull 75: 34-41 Zack M, Boyanovsky BB, Shridas P, Bailey W, Forrest K, Howatt DA, Gelb MH, de Beer FC, Daugherty A, Webb NR (2011) Group X secretory phospholipase A(2) augments angiotensin II-induced inflammatory responses and abdominal aortic aneurysm formation in apoE-deficient mice. Atherosclerosis 214: 58-64 Zhang C, Zhou Z (2002) Ca(2+)-independent but voltage-dependent secretion in mammalian dorsal root ganglion neurons. Nat Neurosci 5: 425-430 Zhang F, Sha J, Wood TG, Galindo CL, Garner HR, Burkart MF, Suarez G, Sierra JC, Agar SL, Peterson JW, Chopra AK (2008) Alteration in the 180 Section V References activation state of new inflammation-associated targets by phospholipase A2-activating protein (PLAA). Cell Signal 20: 844-861 Zhang FY, Wan Y, Zhang ZK, Light AR, Fu KY (2007) Peripheral formalin injection induces long-lasting increases in cyclooxygenase expression by microglia in the spinal cord. J Pain 8: 110-117 Zhang J, Xue R, Ong WY, Chen P (2009) Roles of cholesterol in vesicle fusion and motion. Biophys J 97: 1371-1380 Zhu X, Munoz NM, Rubio N, Herrnreiter A, Mayer D, Douglas I, Leff AR (1996) Quantitation of the cytosolic phospholipase A2 (type IV) in isolated human peripheral blood eosinophils by sandwich-ELISA. J Immunol Methods 199: 119-126 181 [...]... metabolism in brain injury and disorders Subcell Biochem 49 : 241 -268 Adibhatla RM, Hatcher JF, Dempsey RJ (2006) Lipids and lipidomics in brain injury and diseases AAPS J 8: E3 14- 321 Akiba S, Hayama M, Sato T (1998) Inhibition of Ca2+-independent phospholipase A2 by bromoenol lactone attenuates prostaglandin generation induced by interleukin-1 beta and dibutyryl cAMP in rat mesangial cells FEBS Lett 43 7:... classify orofacial pain? In: Lund JP, Lavigne GJ, Dubner R, Sessle BJ (eds) Orofacial pain : from basic science to clinical management ; the transfer of knowledge in pain research to education Quintessence Publishing Co, Inc, Illinois, pp 3- 14 Mechiche H, Naline E, Candenas L, Pinto FM, Birembault P, Advenier C, Devillier P (2003) Effects of cysteinyl leukotrienes in small human bronchus and antagonist... G (1997) Ca2+/phospholipid-binding and syntaxin-binding of native synaptotagmin I Life Sci 61: 711-721 Pruzanski W, Bogoch E, Wloch M, Vadas P (1991) The role of phospholipase A2 in the physiopathology of osteoarthritis J Rheumatol Suppl 27: 117-119 Pruzanski W, Lin KS, Vadas P (1995) Secretory phospholipase A2 in rheumatic diseases In: Glacer KB, Vadas P (eds) Phospholipase A2 in clinical inflammation... effects of snake venom phospholipases A2 Toxicon 27: 613-635 Kinsey GR, Blum JL, Covington MD, Cummings BS, McHowat J, Schnellmann RG (2008) Decreased iPLA2gamma expression induces lipid peroxidation and cell death and sensitizes cells to oxidant-induced apoptosis J Lipid Res 49 : 147 7- 148 7 Kinsey GR, McHowat J, Patrick KS, Schnellmann RG (2007) Role of Ca2+independent phospholipase A2gamma in Ca2+-induced... sPLA2 isozyme, sPLA2-IIA was also observed to be highly involved in nociception Using sPLA2-V as a comparison, the expression profiles of multiple sPLA2 isoforms with the strong secretory signals which included sPLA2-IB, -IIA, -IIC and –X, showed that both mRNA and protein expression of sPLA2-IIA were at high levels in the brainstem and spinal cord Moreover, sPLA2-IIA was also localized in the spinal... at the highest level in the brainstem and spinal cord It was localized in the spinal trigeminal nucleus, further supporting its role in the nociceptive pathway Functionally, sPLA2-III was observed to be involved in pain transmission as the external application of purified form of sPLA2-III, the bee venom, showed an increased membrane capacitance indicating exocytosis sPLA2-III induced exocytosis could... upon orofacial pain induced by facial CA injection Both sPLA2-III and sPLA2-IIA were observed to be the isozymes which play critical roles in the ascending pain pathway Moreover, evidence from this study has shown that sPLA2 could participate in pain transmission via the release of itself or through its enzymatic product, lysophospholipid This study therefore has provided a better understanding of this... Dubner R (eds) Orofacial pain : from basic science to clinical management ; the transfer of knowledge in pain research to education Quintessence Publishing Co, Inc, Illinois, pp 37 -46 Mattson MP, Chan SL (2003) Neuronal and glial calcium signaling in Alzheimer's disease Cell Calcium 34: 385-397 Maxfield FR, Tabas I (2005) Role of cholesterol and lipid organization in disease Nature 43 8: 612-621 Mayer... consistent with an increase in enzyme activity without any changes in enzyme protein expression Together, these findings showed enhanced PLA2 activity in the CM after inflammatory orofacial pain Further study on the expression profile of sPLA2-III in the CNS showed that the enzyme was expressed at the highest level in the medulla oblongata Both mRNA and protein expression of sPLA2-III in normal rat CNS... membrane-associated phospholipase A2 from rat spleen Its comparison with a cytosolic phospholipase A2 S-1 J Biol Chem 263: 5732-5738 Orr JW, Newton AC (1992) Interaction of protein kinase C with phosphatidylserine 1 Cooperativity in lipid binding Biochemistry 31: 46 61 -46 67 Orr SK, Bazinet RP (2008) The emerging role of docosahexaenoic acid in neuroinflammation Curr Opin Investig Drugs 9: 735- 743 Pal S, Sombati . exocytosis and neurotransmitter release in neuroendocrine cells and neurons. In recent findings (in chapter 4) , it showed high levels of sPLA 2 -IIA expression in the brainstem and spinal cord elucidated the role of PLA 2 , sPLA 2 in particular, after orofacial pain. The changes in brain lipids indicating an increased PLA 2 activity was accompanied by an increased expression of sPLA 2 -III in neurotransmission using PC-12 cells. In elucidating the changes in brain lipids, it was observed that there was a decrease in phospholipids including PE and PI species, and an increase in

Ngày đăng: 10/09/2015, 08:30

TỪ KHÓA LIÊN QUAN

TÀI LIỆU CÙNG NGƯỜI DÙNG

TÀI LIỆU LIÊN QUAN

w