Mühl H, Geiger T, Pignat W, Märki F, van den Bosch H, Vosbeck K, Pfeilschifter J
Research Department, Ciba-Geigy Ltd., Basel, Switzerland.
FEBS Lett. 1991 Oct 21;291(2):249-52. doi: 10.1016/0014-5793(91)81295-j.
Treatment of rat mesangial cells with interleukin 1 beta (IL-1 beta) and forskolin greatly enhanced the expression of group II phospholipase A2 (PLA2) mRNA, with subsequent increased synthesis and secretion of PLA2, as detected by PLA2 activity measurements and immunoprecipitation of culture media of [35S]methionine-labelled mesangial cells. PDGF-BB dose-dependently suppressed the IL-1 beta- and forskolin-induced elevation of PLA2 mRNA, as well as PLA2 synthesis and secretion. In contrast, PDGF-AA had no inhibitory effect. The tyrosine kinase inhibitor genistein dose-dependently antagonized the inhibitory effect of PDGF-BB on IL-1 beta-stimulated PLA2 secretion, thus suggesting that tyrosine phosphorylation may be required for PDGF-BB inhibition of PLA2 gene expression in mesangial cells.
用白细胞介素1β(IL - 1β)和福斯高林处理大鼠系膜细胞,可极大地增强II型磷脂酶A2(PLA2)mRNA的表达,随后PLA2的合成和分泌增加,这通过PLA2活性测量以及对[35S]甲硫氨酸标记的系膜细胞培养基进行免疫沉淀检测得出。血小板衍生生长因子BB(PDGF - BB)剂量依赖性地抑制IL - 1β和福斯高林诱导的PLA2 mRNA升高以及PLA2的合成和分泌。相比之下,血小板衍生生长因子AA(PDGF - AA)没有抑制作用。酪氨酸激酶抑制剂染料木黄酮剂量依赖性地拮抗PDGF - BB对IL - 1β刺激的PLA2分泌的抑制作用,因此表明酪氨酸磷酸化可能是PDGF - BB抑制系膜细胞中PLA2基因表达所必需的。