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白细胞介素-4对促炎细胞因子和表皮生长因子刺激的羊膜来源WISH细胞中前列腺素的产生具有差异性调节作用。

Interleukin-4 differentially regulates prostaglandin production in amnion-derived WISH cells stimulated with pro-inflammatory cytokines and epidermal growth factor.

作者信息

Keelan J A, Sato T A, Hansen W R, Gilmour J S, Gupta D K, Helsby N A, Mitchell M D

机构信息

University of Auckland School of Medicine, Department of Pharmacology and Clinical Pharmacology, New Zealand.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 1999 Apr;60(4):255-62. doi: 10.1054/plef.1999.0033.

Abstract

Cytokines and growth factors have been proposed to act as in vivo modulators of amnion prostaglandin production at parturition. To characterize the effects of the 'anti-inflammatory' cytokine interleukin (IL)-4 on amnion prostaglandin production, amnion epithelium-derived WISH cells were treated with IL-4 in the presence/absence of IL-1beta, tumour necrosis factor-alpha (TNF-alpha) or epidermal growth factor (EGF). IL-4 (0.08-10 ng/ml) potently inhibited cytokine-stimulated PGE2 production over 16 h (maximal inhibition approximately 66% at 2.0 ng/ml IL-4). Delaying addition of IL-4 (1 ng/ml) by up to 8 h after IL-1beta addition only slightly attenuated its inhibitory effects, from approximately 65% to approximately 50%. EGF-stimulated PGE2 production was either not inhibited or slightly stimulated by IL-4. Immunoblotting studies revealed that IL-4 (10 ng/ml) significantly suppressed prostaglandin-H synthase-2 (PGHS-2) levels in cells stimulated with IL-1beta and TNF-alpha over 16 h, but had no consistent effects on cytosolic phospholipase A2 (cPLA2) levels under any condition. In the presence of arachidonic acid (10 microM), IL-4 again inhibited cytokine-stimulated, but not EGF-stimulated, PGE2 production. The presence of IL-4 also failed to alter the amount of arachidonic acid released in response to EGF. These findings suggest a role and potential therapeutic application for IL-4 in inhibiting amnion PGHS-2 expression and hence prostaglandin production in infection-driven preterm labour, but not labour in the absence of inflammatory initiators.

摘要

细胞因子和生长因子被认为在分娩时是羊膜前列腺素产生的体内调节剂。为了表征“抗炎”细胞因子白细胞介素(IL)-4对羊膜前列腺素产生的影响,在存在/不存在IL-1β、肿瘤坏死因子-α(TNF-α)或表皮生长因子(EGF)的情况下,用IL-4处理羊膜上皮来源的WISH细胞。IL-4(0.08 - 10 ng/ml)在16小时内有效抑制细胞因子刺激的PGE2产生(在2.0 ng/ml IL-4时最大抑制约66%)。在添加IL-1β后最多延迟8小时添加IL-4(1 ng/ml)只会轻微减弱其抑制作用,从约65%降至约50%。IL-4对EGF刺激的PGE2产生要么没有抑制作用,要么有轻微刺激作用。免疫印迹研究表明,IL-4(10 ng/ml)在16小时内显著抑制IL-1β和TNF-α刺激的细胞中前列腺素-H合成酶-2(PGHS-2)水平,但在任何条件下对细胞质磷脂酶A2(cPLA2)水平均无一致影响。在存在花生四烯酸(10 μM)的情况下,IL-4再次抑制细胞因子刺激的而非EGF刺激的PGE2产生。IL-4的存在也未能改变对EGF反应释放的花生四烯酸量。这些发现表明IL-4在抑制感染驱动的早产中羊膜PGHS-2表达从而抑制前列腺素产生方面具有作用和潜在治疗应用,但在无炎症引发因素的分娩中则不然。

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