Kambe T, Murakami M, Kudo I
Department of Health Chemistry, School of Pharmaceutical Sciences, Showa University, Tokyo, Japan.
FEBS Lett. 1999 Jun 18;453(1-2):81-4. doi: 10.1016/s0014-5793(99)00702-4.
By analyzing human embryonic kidney 293 cell transfectants stably overexpressing various types of phospholipase A2 (PLA2), we have shown that polyunsaturated fatty acids (PUFAs) preferentially activate type IIA secretory PLA2 (sPLA2-IIA)-mediated arachidonic acid (AA) release from interleukin-1 (IL-1)-stimulated cells. When 293 cells prelabeled with 13H]AA were incubated with exogenous PUFAs in the presence of IL-1 and serum, there was a significant increase in [3H]AA release (in the order AA > linoleic acid > oleic acid), which was augmented markedly by sPLA2-IIA and modestly by type IV cytosolic PLA2 (cPLA2), but only minimally by type VI Ca2(+)-independent PLA2, overexpression. Transfection of cPLA2 into sPLA2-IIA-expressing cells produced a synergistic increase in IL-1-dependent [3H]AA release and subsequent prostaglandin production. Our results support the proposal that prior production of AA by cPLA2 in cytokine-stimulated cells destabilizes the cellular membranes, thereby rendering them more susceptible to subsequent hydrolysis by sPLA2-IIA.
通过分析稳定过表达各种类型磷脂酶A2(PLA2)的人胚肾293细胞转染子,我们发现多不饱和脂肪酸(PUFA)优先激活IIA型分泌型磷脂酶A2(sPLA2-IIA)介导的花生四烯酸(AA)从白细胞介素-1(IL-1)刺激的细胞中释放。当用[3H]AA预标记的293细胞在IL-1和血清存在下与外源性PUFA一起孵育时,[3H]AA释放显著增加(顺序为AA>亚油酸>油酸),sPLA2-IIA显著增强,IV型胞质磷脂酶A2(cPLA2)适度增强,但VI型不依赖Ca2+的磷脂酶A2过表达仅轻微增强。将cPLA2转染到表达sPLA2-IIA的细胞中,导致IL-1依赖性[3H]AA释放和随后前列腺素产生协同增加。我们的结果支持以下提议:细胞因子刺激的细胞中cPLA2先前产生的AA使细胞膜不稳定,从而使其更容易受到随后sPLA2-IIA的水解作用。