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磷脂酰肌醇磷酸激酶从细胞膜转移至细胞核。

PIP kinases from the cell membrane to the nucleus.

作者信息

Schramp Mark, Hedman Andrew, Li Weimin, Tan Xiaojun, Anderson Richard

机构信息

Department of Pharmacology, School of Medicine and Public Health, 3710 Medical Sciences Center, University of Wisconsin Medical School, 1300 University Ave., 53706, Madison, WI, USA.

出版信息

Subcell Biochem. 2012;58:25-59. doi: 10.1007/978-94-007-3012-0_2.

Abstract

Phosphatidylinositol 4,5-bisphosphate (PIP(2)) is a membrane bound lipid molecule with capabilities to affect a wide array of signaling pathways to regulate very different cellular processes. PIP(2) is used as a precursor to generate the second messengers PIP(3), DAG and IP(3), indispensable molecules for signaling events generated by membrane receptors. However, PIP(2) can also directly regulate a vast array of proteins and is emerging as a crucial messenger with the potential to distinctly modulate biological processes critical for both normal and pathogenic cell physiology. PIP(2) directly associates with effector proteins via unique phosphoinositide binding domains, altering their localization and/or enzymatic activity. The spatial and temporal generation of PIP(2) synthesized by the phosphatidylinositol phosphate kinases (PIPKs) tightly regulates the activation of receptor signaling pathways, endocytosis and vesicle trafficking, cell polarity, focal adhesion dynamics, actin assembly and 3' mRNA processing. Here we discuss our current understanding of PIPKs in the regulation of cellular processes from the plasma membrane to the nucleus.

摘要

磷脂酰肌醇 -4,5- 二磷酸(PIP₂)是一种膜结合脂质分子,能够影响多种信号通路,以调节截然不同的细胞过程。PIP₂用作生成第二信使PIP₃、二酰基甘油(DAG)和肌醇三磷酸(IP₃)的前体,这些是膜受体产生信号事件所必需的分子。然而,PIP₂也可以直接调节大量蛋白质,并且正成为一种关键信使,有可能显著调节对正常和致病细胞生理学都至关重要的生物学过程。PIP₂通过独特的磷酸肌醇结合结构域直接与效应蛋白结合,改变它们的定位和 / 或酶活性。由磷脂酰肌醇磷酸激酶(PIPK)合成的PIP₂的时空产生严格调节受体信号通路的激活、内吞作用和囊泡运输、细胞极性、粘着斑动态、肌动蛋白组装以及3' mRNA加工。在这里,我们讨论了目前我们对PIPK在从质膜到细胞核的细胞过程调节中的理解。

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