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G蛋白偶联受体与信号网络:新兴范式

G-protein-coupled receptors and signaling networks: emerging paradigms.

作者信息

Marinissen M J, Gutkind J S

机构信息

Oral and Pharyngeal Cancer Branch, National Institute of Dental and Craniofacial Research/NIH, 30 Convent Drive, Building 30, Room 211, Bethesda, MD 20892-4340, USA.

出版信息

Trends Pharmacol Sci. 2001 Jul;22(7):368-76. doi: 10.1016/s0165-6147(00)01678-3.

Abstract

G-protein-coupled receptors (GPCRs) constitute the largest family of cell-surface molecules involved in signal transmission. These receptors play key physiological roles and their dysfunction results in several diseases. Recently, it has been shown that many of the cellular responses mediated by GPCRs do not involve the sole stimulation of conventional second-messenger-generating systems, but instead result from the functional integration of an intricate network of intracellular signaling pathways. Effectors for GPCRs that are independent of G proteins have now also been identified, thus changing the conventional view of the GPCR-heterotrimeric-G-protein-associated effector. The emerging information is expected to help elucidate the most basic mechanism by which these receptors exert their numerous physiological roles, in addition to determining why the perturbation of their function results in many pathological conditions.

摘要

G蛋白偶联受体(GPCRs)构成参与信号转导的最大细胞表面分子家族。这些受体发挥着关键的生理作用,其功能障碍会导致多种疾病。最近的研究表明,许多由GPCRs介导的细胞反应并不涉及对传统第二信使生成系统的单一刺激,而是源于细胞内信号通路复杂网络的功能整合。现已鉴定出独立于G蛋白的GPCRs效应器,从而改变了GPCR-异源三聚体-G蛋白相关效应器的传统观点。除了确定其功能紊乱为何会导致许多病理状况外,这些新出现的信息有望有助于阐明这些受体发挥众多生理作用的最基本机制。

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