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环磷酸腺苷(cAMP)信号在心肌细胞中的功能定位

Functional localization of cAMP signalling in cardiac myocytes.

作者信息

Vandecasteele G, Rochais F, Abi-Gerges A, Fischmeister R

机构信息

INSERM U769, Faculté de Pharmacie, Université de Paris-Sud 11, Châtenay-Malabry, France.

出版信息

Biochem Soc Trans. 2006 Aug;34(Pt 4):484-8. doi: 10.1042/BST0340484.

Abstract

The cAMP pathway is of cardinal importance for heart physiology and pathology. The spatial organization of the various components of the cAMP pathway is thought to allow the segregation of functional responses triggered by the different neuromediators and hormones that use this pathway. PDEs (phosphodiesterases) hydrolyse cAMP (and cGMP) and play a major role in this process by preventing cAMP diffusion to the whole cytosol and inadequate target activation. The development of olfactory cyclic nucleotide-gated channels to directly monitor cAMP beneath the plasma membrane in real time allows us to gain new insights into the molecular mechanisms responsible for cAMP homoeostasis and hormonal specificity in cardiac cells. The present review summarizes the recent results we obtained using this approach in adult rat ventricular myocytes. In particular, the role of PDEs in the maintenance of specific cAMP signals generated by beta-adrenergic receptors and other G(s)-coupled receptors will be discussed.

摘要

环磷酸腺苷(cAMP)信号通路对心脏生理和病理过程至关重要。cAMP信号通路各组分的空间组织被认为能够使利用该通路的不同神经介质和激素所触发的功能反应得以分离。磷酸二酯酶(PDEs)水解cAMP(和cGMP),并通过阻止cAMP扩散至整个细胞质溶胶以及防止靶点过度激活,在这一过程中发挥主要作用。嗅觉环核苷酸门控通道的开发可实时直接监测质膜下的cAMP,这使我们能够对负责心脏细胞中cAMP稳态和激素特异性的分子机制获得新的认识。本综述总结了我们使用这种方法在成年大鼠心室肌细胞中获得 的最新研究结果。特别地 将讨论PDEs在维持由β-肾上腺素能受体和其他G(s)偶联受体产生的特定cAMP信号方面的作用。

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