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垂体腺苷酸环化酶激活多肽通过一条独立于三磷酸肌醇和环磷酸腺苷的新途径,使牛肾上腺髓质细胞中兰尼碱/咖啡因敏感钙库释放钙离子。

Pituitary adenylate cyclase-activating polypeptide causes Ca2+ release from ryanodine/caffeine stores through a novel pathway independent of both inositol trisphosphates and cyclic AMP in bovine adrenal medullary cells.

作者信息

Tanaka K, Shibuya I, Uezono Y, Ueta Y, Toyohira Y, Yanagihara N, Izumi F, Kanno T, Yamashita H

机构信息

Department of Physiology, University of Occupational and Environmental Health School of Medicine, Kitakyusyu, Japan.

出版信息

J Neurochem. 1998 Apr;70(4):1652-61. doi: 10.1046/j.1471-4159.1998.70041652.x.

Abstract

Pituitary adenylate cyclase-activating polypeptide (PACAP) causes both Ca2+ release and Ca2+ influx in bovine adrenal chromaffin cells. To elucidate the mechanisms of PACAP-induced Ca2+ release, we investigated expression of PACAP receptors and measured inositol trisphosphates (IP3), cyclic AMP, and the intracellular Ca2+ concentration in bovine adrenal medullary cells maintained in primary culture. RT-PCR analysis revealed that bovine adrenal medullary cells express the PACAP receptor hop, which is known to couple with both IP3 and cyclic AMP pathways. The two naturally occurring forms of PACAP, PACAP38 and PACAP27, both increased cyclic AMP and IP3, and PACAP38 was more potent than PACAP27 in both effects. Despite the effects of PACAP on IP3 production, the Ca2+ release induced by PA-CAP38 or by PACAP27 was unaffected by cinnarizine, a blocker of IP3 channels. The potencies of the peptides to cause Ca2+ release in the presence of cinnarizine were similar. The Ca2+ release induced by PACAP38 or by PACAP27 was strongly inhibited by ryanodine and caffeine. In the presence of ryanodine and caffeine, PACAP38 was more potent than PACAP27. PACAP-induced Ca2+ release was unaffected by Rp-adenosine 3',5'-cyclic monophosphothioate, an inhibitor of protein kinase A. Ca2+ release induced by bradykinin and angiotensin II was also inhibited by ryanodine and caffeine, but unaffected by cinnarizine. Although IP3 production stimulated by PACAP38 or bradykinin was abolished by the phospholipase C inhibitor, U-73122, Ca2+ release in response to the peptides was unaffected by U-73122. These results suggest that PACAP induces Ca2+ release from ryanodine/caffeine stores through a novel intracellular mechanism independent of both IP3 and cyclic AMP and that the mechanism may be the common pathway through which peptides release Ca2+ in adrenal chromaffin cells.

摘要

垂体腺苷酸环化酶激活多肽(PACAP)可引起牛肾上腺嗜铬细胞内钙离子释放及钙离子内流。为阐明PACAP诱导钙离子释放的机制,我们研究了PACAP受体的表达,并检测了原代培养的牛肾上腺髓质细胞中三磷酸肌醇(IP3)、环磷酸腺苷(cAMP)及细胞内钙离子浓度。逆转录聚合酶链反应(RT-PCR)分析显示,牛肾上腺髓质细胞表达PACAP受体hop,已知该受体可与IP3及环磷酸腺苷途径偶联。两种天然存在的PACAP形式,即PACAP38和PACAP27,均可增加环磷酸腺苷及IP3,且在这两种效应中PACAP38比PACAP27更有效。尽管PACAP对IP3生成有影响,但由PACAP38或PACAP27诱导的钙离子释放不受IP3通道阻滞剂桂利嗪的影响。在存在桂利嗪的情况下,这些肽引起钙离子释放的效力相似。由PACAP38或PACAP27诱导的钙离子释放受到ryanodine和咖啡因的强烈抑制。在存在ryanodine和咖啡因的情况下,PACAP38比PACAP27更有效。PACAP诱导的钙离子释放不受蛋白激酶A抑制剂Rp-腺苷3',5'-环磷酸硫代酯的影响。缓激肽和血管紧张素II诱导的钙离子释放也受到ryanodine和咖啡因的抑制,但不受桂利嗪的影响。尽管PACAP38或缓激肽刺激产生的IP3生成被磷脂酶C抑制剂U-73122消除,但对这些肽的钙离子释放反应不受U-73122影响。这些结果表明,PACAP通过一种独立于IP3和环磷酸腺苷的新型细胞内机制从ryanodine/咖啡因敏感储存库诱导钙离子释放,且该机制可能是肽类在肾上腺嗜铬细胞中释放钙离子的共同途径。

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