1998
DOI: 10.1074/jbc.273.23.14411
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The Functions of Five Distinct Mammalian Phospholipase A2s in Regulating Arachidonic Acid Release

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Cited by 352 publications
(299 citation statements)
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“…Unlike sPLA 2 IIa, however, sPLA 2 V binds efficiently to the major phospholipid (PC) in membranes and lipoproteins [10], and therefore may be physiologically more relevant in phospholipid turnover and eicosanoid synthesis. Balboa et al [8] showed that the arachidonate release and prostaglandin production in mouse macrophage cell line P388D was dependent upon the presence of sPLA 2 V. Similarly, Murakami et al [11] reported that in fibroblasts and CHO cells, sPLA 2 V acts in concert with the cytosolic PLA 2 in the release of arachidonate. sPLA 2 V also has strong affinity to proteoglycans on the cell surface, and this property appears to be critical for its function [11].…”
Section: Discussionmentioning
confidence: 96%
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“…Unlike sPLA 2 IIa, however, sPLA 2 V binds efficiently to the major phospholipid (PC) in membranes and lipoproteins [10], and therefore may be physiologically more relevant in phospholipid turnover and eicosanoid synthesis. Balboa et al [8] showed that the arachidonate release and prostaglandin production in mouse macrophage cell line P388D was dependent upon the presence of sPLA 2 V. Similarly, Murakami et al [11] reported that in fibroblasts and CHO cells, sPLA 2 V acts in concert with the cytosolic PLA 2 in the release of arachidonate. sPLA 2 V also has strong affinity to proteoglycans on the cell surface, and this property appears to be critical for its function [11].…”
Section: Discussionmentioning
confidence: 96%
“…Balboa et al [8] showed that the arachidonate release and prostaglandin production in mouse macrophage cell line P388D was dependent upon the presence of sPLA 2 V. Similarly, Murakami et al [11] reported that in fibroblasts and CHO cells, sPLA 2 V acts in concert with the cytosolic PLA 2 in the release of arachidonate. sPLA 2 V also has strong affinity to proteoglycans on the cell surface, and this property appears to be critical for its function [11]. The enzyme has been reported to be present in atherosclerotic lesions [28], and may be involved in the conversion of LDL to a more atherogenic particle [29].…”
Section: Discussionmentioning
confidence: 96%
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“…These chimeras were expressed in Chinese hamster ovary (CHO) cells overproducing the G-protein-coupled a 2B adrenergic receptor (CHO-2B cells). CHO cells contain three forms of PLA 2 s, like many other cell types, and they seem to play different roles in D 4 Ach release: an sPLA 2 , which is not involved in rapid receptor-mediated D 4 Ach release [4,21], an iPLA 2 [22], which q FEBS 1999 is mainly involved in the remodeling of membrane phospholipids [23], and cPLA 2 , which is responsible for D 4 Ach release after stimulation by extracellular agonists or an increase in intracellular Ca 2+ [4,5]. In CHO-2B cells it was possible to separately induce receptor-mediated phosphorylation and activation of cPLA 2 by Ca 2 [24].…”
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confidence: 99%
“…Recent evidence indicates that cPLA 2 plays a major role in the overproduction of lipid mediators during inflammation [2,3]. cPLA 2 activated by extracellular stimuli triggers the rapid hydrolysis of membrane phospholipids to give free arachidonic acid (D 4 Ach), which is the rate-limiting step of eicosanoid production [4,5]. This activation is dependent on at least two mechanisms: the phosphorylation of cPLA 2 by various kinases and its translocation to membrane phospholipids by a Ca 2+ -dependent lipid-binding domain (CaLB domain) [6], following an increase in intracellular Ca 2+.…”
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confidence: 99%