Mechanisms that account for the selective release of arachidonic acid from intact cells by secretory phospholipase A2

被引:30
|
作者
Fonteh, AN
Samet, JM
Surette, M
Reed, W
Chilton, FH
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Internal Med, Div Pulm & Crit Care Med, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27157 USA
[3] Univ N Carolina, Ctr Environm Med & Lung Biol, Chapel Hill, NC 27599 USA
关键词
arachidonic acid; mast cell; secretory phospholipase A(2); secretory phospholipase A(2) receptor;
D O I
10.1016/S0005-2760(98)00079-4
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
The current study examined mechanisms that account for the selective release of arachidonic acid (AA) from cells by secretory phospholipase A(2) (sPLA(2)). Initial studies demonstrated that low concentrations of group I and group III PLA(2) isotypes and an sPLA(2)-enriched extract from bone marrow-derived mast cells (BMMC) selectively released AA from mast cells. Much higher concentrations of group II PLA(2) were required to release comparable quantities of AA. Group I PLA(2) also selectively released AA from another mast cell line (CFTL-15) and a monocytic cell line (THP-1). In contrast, high concentrations of group I PLA(2) were required to release fatty acids from a promyelocytic cell line (HL-60) and this release was not selective for AA. Binding studies revealed that cell types (BMMC, CFTL-15 and THP-I) which selectively released AA also had the capacity to specifically bind group I PLA(2). However, group II PLA(2), which did not selectively release AA from cells, also did not specifically bind to these same cell types. Additional studies revealed that sPLA(2) binding to the mast cell receptor was attenuated after stimulation with antigen or ionophore A23187. Reverse transcriptase-polymerase chain reaction analyses indicated the presence of mRNA for the sPLA(2) receptor in BMMC, CFTL-15 and THP-1 and the absence of this mRNA in HL-60. Final studies demonstrated that p-aminophenyl-alpha-D-mannopyranoside BSA, a known ligand of the sPLA(2) receptor, also selectively released AA from mast cells but not from HL-60 cells. These experiments indicated that receptor occupancy alone (without PLA(2) activity) is sufficient to induce the release of AA from mast cells. Together, these data reveal that specific isotypes of sPLA(2) have the capacity to selectively release AA from certain cells by their capacity to bind to sPLA(2) receptors on the cell surface. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:253 / 266
页数:14
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