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磷脂酰肌醇4,5-二磷酸水平的调控及其在细胞骨架重组和恶性转化中的作用。

Regulation of phosphatidylinositol 4,5-bisphosphate levels and its roles in cytoskeletal re-organization and malignant transformation.

作者信息

Takenawa T, Itoh T, Fukami K

机构信息

Department of Biochemistry, University of Tokyo, Japan.

出版信息

Chem Phys Lipids. 1999 Apr;98(1-2):13-22. doi: 10.1016/s0009-3084(99)00014-6.

Abstract

It is well known that phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) plays important roles not only as a precursor lipid for generating second messengers but also as a regulator of cytoskeletal re-organization. The last step of PtdIns(4,5)P2 synthesis is catalyzed by PtdIns monophosphate(PIP) kinase. So far, three type I PIP kinases(alpha, beta, and gamma), which phosphorylate PtdIns(4) to PtdIns(4,5)P2, and three type II PIP kinases(alpha, beta, gamma), which phosphorylate PtdIns(5)P to PtdIns(4,5)P2 have been found. On the other hand, several inositolpolyphosphate 5-phosphatases which convert PtdIns(4,5)P2 to PtdIns(4) are known. Among them, synaptojanin, which associates with tyrosine kinase receptors through an adaptor protein, Ash/Grb2, in response to growth factors, is capable of hydrolyzing PtdIns(4,5)P2 bound to actin regulatory proteins, resulting in actin filament re-organization downstream of tyrosine kinases.

摘要

众所周知,磷脂酰肌醇-4,5-二磷酸(PtdIns(4,5)P2)不仅作为生成第二信使的前体脂质发挥重要作用,还作为细胞骨架重组的调节剂。PtdIns(4,5)P2合成的最后一步由磷脂酰肌醇单磷酸(PIP)激酶催化。到目前为止,已发现三种I型PIP激酶(α、β和γ),它们将磷脂酰肌醇-4(PtdIns(4))磷酸化为PtdIns(4,5)P2,以及三种II型PIP激酶(α、β、γ),它们将磷脂酰肌醇-5-磷酸(PtdIns(5)P)磷酸化为PtdIns(4,5)P2。另一方面,已知几种将PtdIns(4,5)P2转化为PtdIns(4)的肌醇多磷酸5-磷酸酶。其中,突触素结合蛋白可通过接头蛋白Ash/Grb2与酪氨酸激酶受体结合,以响应生长因子,它能够水解与肌动蛋白调节蛋白结合的PtdIns(4,5)P2,从而导致酪氨酸激酶下游的肌动蛋白丝重组。

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