Lim L K, Hunt N H, Eichner R D, Weidemann M J
Biochem Biophys Res Commun. 1983 Jul 18;114(1):248-54. doi: 10.1016/0006-291x(83)91620-0.
The ionophore A23187 (6.7 microM) increased the rates of formation of prostaglandins and cyclic AMP in suspensions of thioglycollate-elicited rat peritoneal macrophages. Both effects were inhibited by the calmodulin blocker trifluoperazine (50 microM) and the calcium channel blocker verapamil (500 microM). Inhibitors of phospholipase A2 and cyclo-oxygenase also blocked both actions of A23187. The stimulated prostaglandin formation was markedly reduced when the cells were preincubated with 8-bromo-cyclic AMP (1mM), dibutyryl cyclic AMP (1mM) or cholera toxin (500ng/ml). Addition of exogenous arachidonic acid (30 microM) alleviated this inhibition. We propose that the effect of A23187 on macrophages includes a 'self-limiting' mechanism whereby newly-synthesized prostaglandins can inhibit, via cyclic AMP, a step(s) prior to the transformation of arachidonic acid and thus modulate their own production.
离子载体A23187(6.7微摩尔)可提高巯基乙酸诱导的大鼠腹腔巨噬细胞悬液中前列腺素和环磷酸腺苷(cAMP)的生成速率。这两种效应均被钙调蛋白阻滞剂三氟拉嗪(50微摩尔)和钙通道阻滞剂维拉帕米(500微摩尔)所抑制。磷脂酶A2和环氧化酶的抑制剂也可阻断A23187的这两种作用。当细胞预先与8-溴环磷酸腺苷(1毫摩尔)、二丁酰环磷酸腺苷(1毫摩尔)或霍乱毒素(500纳克/毫升)孵育时,刺激的前列腺素生成明显减少。添加外源性花生四烯酸(30微摩尔)可减轻这种抑制作用。我们提出,A23187对巨噬细胞的作用包括一种“自我限制”机制,即新合成的前列腺素可通过环磷酸腺苷抑制花生四烯酸转化之前的一个或多个步骤,从而调节其自身的产生。