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酪氨酸磷酸化对肌醇1,4,5-三磷酸受体的调控

Regulation of the inositol 1,4,5-trisphosphate receptor by tyrosine phosphorylation.

作者信息

Jayaraman T, Ondrias K, Ondriasová E, Marks A R

机构信息

Laboratory for Molecular Cardiology, Department of Medicine, Mount Sinai School of Medicine, New York 10029, USA.

出版信息

Science. 1996 Jun 7;272(5267):1492-4. doi: 10.1126/science.272.5267.1492.

Abstract

Tyrosine kinases indirectly raise intracellular calcium concentration ([Ca2+]i) by activating phospholipases that generate inositol 1,4,5-trisphosphate (IP3). IP3 activates the IP3 receptor (IP3R), an intracellular calcium release channel on the endoplasmic reticulum. T cell receptor stimulation triggered a physical association between the nonreceptor protein tyrosine kinase Fyn and the IP3R, which induced tyrosine phosphorylation of the IP3R. Fyn activated an IP3-gated calcium channel in vitro, and tyrosine phosphorylation of the IP3R during T cell activation was reduced in thymocytes from fyn-/- mice. Thus, activation of the IP3R by tyrosine phosphorylation may play a role in regulating [Ca2+]i.

摘要

酪氨酸激酶通过激活产生肌醇1,4,5-三磷酸(IP3)的磷脂酶间接提高细胞内钙浓度([Ca2+]i)。IP3激活IP3受体(IP3R),这是一种位于内质网上的细胞内钙释放通道。T细胞受体刺激引发了非受体蛋白酪氨酸激酶Fyn与IP3R之间的物理结合,从而诱导IP3R的酪氨酸磷酸化。Fyn在体外激活了IP3门控钙通道,并且在fyn-/-小鼠的胸腺细胞中,T细胞激活过程中IP3R的酪氨酸磷酸化减少。因此,酪氨酸磷酸化对IP3R的激活可能在调节[Ca2+]i中发挥作用。

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