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安乐蜥黑素细胞上促黑素细胞激素受体的光亲和标记:儿茶酚胺、钙和福斯高林的作用

Photoaffinity labelling of MSH receptors on Anolis melanophores: effects of catecholamines, calcium and forskolin.

作者信息

Eberle A N, Girard J

出版信息

J Recept Res. 1985;5(1):59-81. doi: 10.3109/10799898509041871.

Abstract

Photoaffinity labelling of MSH receptors on Anolis melanophores was used as a tool for studying the effects of catecholamines, calcium and forskolin on hormone-receptor interaction and receptor-adenylate cyclase coupling. Covalent attachment of photoreactive alpha-MSH to its receptor was suppressed in calcium-free buffer but was hardly influenced by catecholamines or forskolin. The longlasting signal generated by the covalent MSH-receptor complex was readily and reversibly abolished by adrenaline, noradrenaline, dopamine or clonidine or by the absence of calcium. The suppression of pigment dispersion by catecholamines was blocked by the simultaneous presence of yohimbine but not prazosin, indicating that the catecholamines antagonize the alpha-MSH signal by inhibitory action on the adenylate cyclase system through an alpha-2 receptor. Forskolin, which stimulates melanophores by direct action on the catalytic unit of the adenylate cyclase and at about the same speed as alpha-MSH, produced a slower and weaker response in the presence of noradrenaline. If MSH receptors were covalently labelled and then exposed to noradrenaline, the characteristics of the forskolin-induced response were identical to those of unlabelled cells that had not been exposed to noradrenaline. This may point to a partial restoration of receptor-adenylate cyclase coupling by forskolin. The results show that the longlasting stimulation of Anolis melanophores by photoaffinity labelling proceeds via a permanently stimulated adenylate-cyclase system whose coupling to the receptor depends on calcium and is abolished by alpha-2 receptor agonists. Calcium is also essential for hormone-receptor binding.

摘要

利用光亲和标记法标记绿安乐蜥黑素细胞上的促黑素(MSH)受体,作为研究儿茶酚胺、钙和福斯高林对激素-受体相互作用以及受体-腺苷酸环化酶偶联作用的工具。在无钙缓冲液中,光反应性α-MSH与其受体的共价结合受到抑制,但儿茶酚胺或福斯高林对其影响不大。由共价MSH-受体复合物产生的持久信号很容易被肾上腺素、去甲肾上腺素、多巴胺或可乐定或通过去除钙而可逆地消除。育亨宾同时存在时可阻断儿茶酚胺对色素分散的抑制作用,而哌唑嗪则不能,这表明儿茶酚胺通过α-2受体对腺苷酸环化酶系统的抑制作用来拮抗α-MSH信号。福斯高林通过直接作用于腺苷酸环化酶的催化单位来刺激黑素细胞,其作用速度与α-MSH大致相同,在去甲肾上腺素存在的情况下,产生的反应较慢且较弱。如果MSH受体被共价标记,然后暴露于去甲肾上腺素,福斯高林诱导的反应特征与未暴露于去甲肾上腺素的未标记细胞相同。这可能表明福斯高林可部分恢复受体-腺苷酸环化酶的偶联。结果表明,通过光亲和标记对绿安乐蜥黑素细胞进行的长期刺激是通过一个永久受刺激的腺苷酸环化酶系统进行的,该系统与受体的偶联依赖于钙,并被α-2受体激动剂所消除。钙对于激素-受体结合也至关重要。

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