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肌醇三磷酸受体与细胞内钙离子信号传导

The InsP3 receptor and intracellular Ca2+ signaling.

作者信息

Mikoshiba K

机构信息

Department of Molecular Neurobiology, Institute of Medical Science University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo, 108, Japan.

出版信息

Curr Opin Neurobiol. 1997 Jun;7(3):339-45. doi: 10.1016/s0959-4388(97)80061-x.

Abstract

The inositol 1,4,5-trisphosphate receptor (InsP3R) is a ligand-gated Ca2+-release channel on intracellular Ca2+ store sites (such as the endoplasmic reticulum), and plays an important role in intracellular Ca2+ signaling in a wide variety of cell types. Recent studies have shown that binding of inositol 1,4,5-trisphosphate (InsP3) to InsP3R isoforms is differentially regulated by Ca2+, and that InsP3R functions are finely regulated by phosphorylation via tyrosine kinases and protein kinase C, by dephosphorylation via calcineurin, and by binding to FKBP (FK506-binding protein). In addition, transient receptor potential (TRP) and TRP-like proteins appear to couple conformationally with the InsP3R for capacitative Ca2+ entry. The importance of InsP3R signaling in neuronal function has been demonstrated by gene targeting in mice and by studies of T-cell receptor signaling, apoptosis, meiotic maturation, and cytokinesis.

摘要

肌醇1,4,5-三磷酸受体(InsP3R)是细胞内钙储存位点(如内质网)上的一种配体门控钙释放通道,在多种细胞类型的细胞内钙信号传导中发挥重要作用。最近的研究表明,肌醇1,4,5-三磷酸(InsP3)与InsP3R亚型的结合受Ca2+的差异调节,并且InsP3R的功能通过酪氨酸激酶和蛋白激酶C的磷酸化、钙调神经磷酸酶的去磷酸化以及与FKBP(FK506结合蛋白)的结合而受到精细调节。此外,瞬时受体电位(TRP)和TRP样蛋白似乎在构象上与InsP3R偶联,以实现容量性钙内流。通过小鼠基因靶向以及对T细胞受体信号传导、细胞凋亡、减数分裂成熟和胞质分裂的研究,已证明InsP3R信号传导在神经元功能中的重要性。

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