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钙敏感受体与钙振荡:作为第一信使的钙

Calcium sensing receptors and calcium oscillations: calcium as a first messenger.

作者信息

Breitwieser Gerda E

机构信息

Weis Center for Research, Geisinger Clinic, Danville, Pennsylvania 17822, USA.

出版信息

Curr Top Dev Biol. 2006;73:85-114. doi: 10.1016/S0070-2153(05)73003-9.

Abstract

Calcium sensing receptors (CaR) are unique among G-protein-coupled receptors (GPCRs) since both the first (extracellular) and second (intracellular) messengers are Ca(2+). CaR serves to translate small fluctuations in extracellular Ca(2+) into intracellular Ca(2+) oscillations. In many cells and tissues, CaR also acts as a coincidence detector, sensing both changes in extracellular Ca(2+) plus the presence of various allosteric activators including amino acids, polyamines, and/or peptides. CaR oscillations are uniquely shaped by the activating agonist, that is, Ca(2+) triggers sinusoidal oscillations while Ca(2+) plus phenylalanine trigger transient oscillations of lower frequency. The distinct oscillation patterns generated by Ca(2+)versus Ca(2+) plus phenylalanine are the results of activation of distinct signal transduction pathways. CaR is a member of Family C GPCRs, having a large extracellular agonist binding domain, and functioning as a disulfide-linked dimer. The CaR dimer likely can be driven to distinct active conformations by various Ca(2+) plus modulator combinations, which can drive preferential coupling to divergent signaling pathways. Such plasticity with respect to both agonist and signaling outcomes allows CaR to uniquely contribute to the physiology of organs and tissues where it is expressed. This chapter will examine the structural features of CaR, which contribute to its unique properties, the nature of CaR-induced intracellular Ca(2+) signals and the potential role(s) for CaR in development and differentiation.

摘要

钙敏感受体(CaR)在G蛋白偶联受体(GPCR)中独具特色,因为第一信使(细胞外)和第二信使(细胞内)均为Ca²⁺。CaR可将细胞外Ca²⁺的微小波动转化为细胞内Ca²⁺振荡。在许多细胞和组织中,CaR还充当一种巧合探测器,既能感知细胞外Ca²⁺的变化,又能检测包括氨基酸、多胺和/或肽在内的各种变构激活剂的存在。CaR振荡由激活激动剂独特塑造,即Ca²⁺触发正弦振荡,而Ca²⁺加苯丙氨酸触发低频瞬态振荡。Ca²⁺与Ca²⁺加苯丙氨酸产生的不同振荡模式是不同信号转导途径激活的结果。CaR是C类GPCR成员,具有大的细胞外激动剂结合结构域,以二硫键连接的二聚体形式发挥作用。CaR二聚体可能会被各种Ca²⁺加调节剂组合驱动到不同的活性构象,这可驱动其优先偶联到不同的信号转导途径。这种在激动剂和信号转导结果方面的可塑性使CaR能够独特地影响其表达所在器官和组织的生理学。本章将探讨CaR的结构特征,这些特征促成了其独特性质、CaR诱导的细胞内Ca²⁺信号的性质以及CaR在发育和分化中的潜在作用。

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