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Lipopolysaccharide-induced release of arachidonic acid and prostaglandins in liver macrophages: Regulation by Group IV cytosolic phospholipase A(2), but not by Group V and Group IIA secretory phospholipase A(2)

机译:脂多糖诱导肝巨噬细胞中花生四烯酸和前列腺素的释放:由IV组胞质磷脂酶A(2)调节,但不受V组和IIA组分泌型磷脂酶A(2)调节

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Lipopolysaccharide (LPS) induces a delayed release (lag phase of 2-4 h) of arachidonic acid (AA) and prostaglandin (PG) D-2 in rat liver macrophages. Group IV cytosolic phospholipase A(2) (cPLA(2)) becomes phosphorylated within minutes after the addition of LPS. The phosphorylated form of cPLA(2) shows an enhanced in vitro activity. The Ca2+ dependence of cPLA(2) activity is not affected by phosphorylation of the enzyme. In addition, LPS induces an enhanced expression of cPLA(2) mRNA (after 2-4 h) and an enhanced expression of cPLA(2) protein (after 8 h). The cellular cPLA(2) activity is enhanced about twofold 24 h after LPS treatment. Liver macrophages constitutively express mRNAs encoding Groups V and IIA secretory PLA(2) (sPLA,). LPS has no effect on the levels of Groups V and HA sPLA(2) mRNA expression. Despite mRNA expression, Groups V and IIA sPLA(2) protein and sPLA(2) activity are not detectable in unstimulated or LPS-stimulated liver macrophages. Collectively, these and earlier [Mediators Inflammation 8 (1999) 295.] results suggest that in liver macrophages the LPS-induced delayed release of AA and prostanoids is mediated by phosphorylation and an enhanced expression of cPLA(2), a de novo expression of cyclooxygenase (COX)-2, but not by the actions of Group V or Group IIA sPLA(2). (C) 2002 Elsevier Science Inc. All rights reserved. [References: 24]
机译:脂多糖(LPS)诱导大鼠肝巨噬细胞中花生四烯酸(AA)和前列腺素(PG)D-2的延迟释放(延迟阶段为2-4小时)。添加LPS后几分钟内,IV组胞质磷脂酶A(2)(cPLA(2))磷酸化。 cPLA(2)的磷酸化形式表现出增强的体外活性。 CaPLA(2)活动的Ca 2 +依赖不受该酶的磷酸化的影响。此外,LPS诱导cPLA(2)mRNA的增强表达(2-4小时后)和cPLA(2)蛋白的增强表达(8小时后)。 LPS治疗后约24小时,细胞cPLA(2)活性增强。肝巨噬细胞组成性表达编码V组和IIA分泌PLA(2)(sPLA,)的mRNA。 LPS对V组和HA sPLA(2)mRNA表达水平没有影响。尽管mRNA表达,V组和IIA sPLA(2)蛋白和sPLA(2)活性在未刺激或LPS刺激的肝巨噬细胞中均未检出。这些和更早的结果[Mediators Inflammation 8(1999)295.]共同表明,在肝巨噬细胞中,LPS诱导的AA和前列腺素类药物的延迟释放是由磷酸化和cP​​LA(2)的重新表达介导的,从头开始表达环氧化酶(COX)-2,但不受第V组或IIA组sPLA(2)的作用。 (C)2002 Elsevier Science Inc.保留所有权利。 [参考:24]

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