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反馈调节因子对腺苷酸环化酶的作用。

Action of feedback regulator on adenylate cyclase.

作者信息

Ho R J, Sutherland E W

出版信息

Proc Natl Acad Sci U S A. 1975 May;72(5):1773-7. doi: 10.1073/pnas.72.5.1773.

Abstract

A factor [the feedback regulator (FR)] formed by adipocytes after the stimulation of a cAMP raising hormone has been found to be a potent inhibitor of membrane-bound adenylate cyclase [EC 4.6.1.1.; ATP pyrophosphate-lyase (cyclizing)]. In a standard assay system using rat adipocyte plasma membrane as the source of adenylate cyclase, the FR inhibited adenylate cyclase by lowering the Vmax without affecting the apparent Km for ATP (0.3-0.6 mM). The apparent Ka for epinephrine (5-6 muM) was also not affected by FR. The inhibitory action of FR was partially countered by Mg2+ ions. An increase in phosphorylation of plasma membrane was observed when FR was present in the incubation system. The concentration required for a 50% inhibition was four times higher when adenosine 5-(beta,gamma-imino) triphosphate [AMP-P(NH)P] replaced ATP as the substrate for adenylate cyclase, implying that adenylate cyclase was inactivated by phosphorylation caused by FR. Increase in FR inhibition obtained by adding low concentrations of adenosine 5-(alpha,beta-methylene) triphosphate or ATP to AMP-(NH)P as the substrate supports this view. The inhibitory action was reversible. These results are consistent with the previously reported phenomena that (1) the undue to the formation of FR, and (2) the recovery of responsiveness of the stimulated cells by washing the cells with regular buffer medium is a result of the removal of FR. The hormone-initiated biphasic curve of cAMP levels in adipocytes is believed to be due to the negative feedback action of FR on adenylate cyclase. The mechanism of action of FR on inhibition of adenylate cyclase appears to be related to the phosphorylation of certain membrane components.

摘要

已发现一种由脂肪细胞在环磷酸腺苷(cAMP)升高激素刺激后形成的因子[反馈调节因子(FR)]是膜结合腺苷酸环化酶(EC 4.6.1.1;ATP焦磷酸裂解酶(环化))的强效抑制剂。在以大鼠脂肪细胞质膜作为腺苷酸环化酶来源的标准测定系统中,FR通过降低Vmax来抑制腺苷酸环化酶,而不影响ATP(0.3 - 0.6 mM)的表观Km。FR对肾上腺素(5 - 6 μM)的表观Ka也没有影响。FR的抑制作用部分被Mg2 +离子抵消。当孵育系统中存在FR时,观察到质膜磷酸化增加。当腺苷5 -(β,γ - 亚氨基)三磷酸[AMP - P(NH)P]替代ATP作为腺苷酸环化酶的底物时,50%抑制所需的浓度高出四倍,这意味着腺苷酸环化酶因FR引起的磷酸化而失活。通过向作为底物的AMP -(NH)P中添加低浓度的腺苷5 -(α,β - 亚甲基)三磷酸或ATP获得的FR抑制作用增强支持了这一观点。抑制作用是可逆的。这些结果与先前报道的现象一致,即(1)FR形成的影响,以及(2)用常规缓冲介质洗涤细胞后受刺激细胞反应性的恢复是FR去除的结果。脂肪细胞中cAMP水平的激素引发的双相曲线被认为是由于FR对腺苷酸环化酶的负反馈作用。FR抑制腺苷酸环化酶的作用机制似乎与某些膜成分的磷酸化有关。

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Action of feedback regulator on adenylate cyclase.反馈调节因子对腺苷酸环化酶的作用。
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