Identification of a third pathway for arachidonic acid mobilization and prostaglandin production in activated P388D1 macrophage-like cells

被引:63
作者
Balsinde, J [1 ]
Balboa, MA
Dennis, EA
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, Revelle Coll, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, La Jolla, CA 92093 USA
关键词
D O I
10.1074/jbc.M910163199
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies have demonstrated that P388D(1) macrophages are able to mobilize arachidonic acid (AA) and synthesize prostaglandins in two temporally distinct phases. The first phase is triggered by platelet-activating factor within minutes, but needs the cells to be previously exposed to bacterial lipopolysaccharide (LPS) for periods up to 1 h, It is thus a primed immediate phase. The second, delayed phase occurs in response to LPS alone over long incubation periods spanning several hours. Strikingly, the effector enzymes involved in both of these phases are the same, namely the cytosolic group IV phospholipase A(2) (cPLA(2)), the secretory group V phospholipase A(2), and cyclooxygenase-2, although the regulatory mechanisms differ. Here we report that P388D(1) macrophages mobilize AA and produce prostaglandins in response to zymosan particles in a manner that is clearly different from the two described above. Zymosan triggers an immediate AA mobilization response from the macrophages that neither involves the group v phospholipase A(2) nor requires the cells to be primed by LPS, The group VI Ca2+-independent phospholipase A(2) is also not involved. Zymosan appears to signal exclusively through activation of the cPLA(2), which is coupled to the cyclooxygenase-2, These results define a secretory PLA(2)-independent pathway for AA mobilization in the P388D(1) macrophages, and demonstrate that, under certain experimental settings, stimulation of the cPLA(2) is sufficient to generate a prostaglandin biosynthetic response in the P388D(1) macrophages.
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页码:22544 / 22549
页数:6
相关论文
共 41 条
[1]  
AIZOLA E, 1998, J BIOL CHEM, V273, P30208
[2]   Involvement of group VICa2+-independent phospholipase A2 in protein kinase C-dependent arachidonic acid liberation in zymosan-stimulated macrophage-like P388D1 cells [J].
Akiba, S ;
Mizunaga, S ;
Kume, K ;
Hayama, M ;
Sato, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (28) :19906-19912
[3]   Cellular responses to excess phospholipid [J].
Baburina, I ;
Jackowski, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (14) :9400-9408
[4]   Regulation of arachidonic acid mobilization in lipopolysaccharide-activated P388D1 macrophages by adenosine triphosphate [J].
Balboa, MA ;
Balsinde, J ;
Johnson, CA ;
Dennis, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) :36764-36768
[5]   Novel group V phospholipase A(2) involved in arachidonic acid mobilization in murine P388D(1) macrophages [J].
Balboa, MA ;
Balsinde, J ;
Winstead, MV ;
Tischfield, JA ;
Dennis, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :32381-32384
[6]   Identity between the Ca2+-independent phospholipase A(2) enzymes from P388D(1) macrophages and Chinese hamster ovary cells [J].
Balboa, MA ;
Balsinde, J ;
Jones, SS ;
Dennis, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (13) :8576-8580
[7]  
Balsinde J, 1997, ADV EXP MED BIOL, V407, P99
[8]   The incorporation of arachidonic acid into triacylglycerol in P388D(1) macrophage-like cells [J].
Balsinde, J ;
Dennis, EA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 235 (03) :480-485
[9]   Regulation and inhibition of phospholipase A2 [J].
Balsinde, J ;
Balboa, MA ;
Insel, PA ;
Dennis, EA .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1999, 39 :175-189
[10]   PATHWAYS FOR ARACHIDONIC-ACID MOBILIZATION IN ZYMOSAN-STIMULATED MOUSE PERITONEAL-MACROPHAGES [J].
BALSINDE, J ;
FERNANDEZ, B ;
SOLISHERRUZO, JA ;
DIEZ, E .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1136 (01) :75-82