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SRC家族激酶的表达降低会降低NBS1基因敲除淋巴母细胞中的PI3K活性。

Reduced expression of SRC family kinases decreases PI3K activity in NBS1-/- lymphoblasts.

作者信息

Sagan Daniel, Eckardt-Schupp Friederike, Eichholtz-Wirth Hedda

机构信息

Institute of Radiation Biology, Helmholtz Centre Munich, Neuherberg, Germany.

出版信息

Biochem Biophys Res Commun. 2008 Dec 5;377(1):181-6. doi: 10.1016/j.bbrc.2008.09.098. Epub 2008 Oct 1.

Abstract

SRC family kinases (SFKs) are involved in the activation of phosphatidylinositol-3-kinase (PI3K). In addition, the activity of this lipid kinase can be regulated by the DNA repair protein NBS1. Here, we describe a disturbed expression of some members of the non-receptor tyrosine kinase family in lymphoblastoid cell lines generated from cells of Nijmegen breakage syndrome (NBS) patients. Especially, only minor amounts of the kinases LCK and HCK are expressed in the NBS1(-/-) cell lines as compared to the consanguineous NBS1(+/-) cells. We demonstrate that SFK activity is important for a proper activation of PI3K in these cells and that it is reduced in NBS1(-/-) cells. We provide evidence that the observed reduced PI3K activity in NBS lymphoblasts is caused by an impaired expression of the SFKs LCK and/or HCK. Thus, our data establish a new function for the NBS1 protein as a regulator of PI3K activity via SFK members.

摘要

Src家族激酶(SFKs)参与磷脂酰肌醇-3-激酶(PI3K)的激活。此外,这种脂质激酶的活性可受DNA修复蛋白NBS1的调节。在此,我们描述了在尼曼-匹克氏症(NBS)患者细胞产生的淋巴母细胞系中非受体酪氨酸激酶家族某些成员的表达紊乱。尤其是,与近亲的NBS1(+/-)细胞相比,NBS1(-/-)细胞系中仅表达少量的LCK和HCK激酶。我们证明,SFK活性对于这些细胞中PI3K的适当激活很重要,并且在NBS1(-/-)细胞中其活性降低。我们提供的证据表明,在NBS淋巴细胞中观察到的PI3K活性降低是由SFKs LCK和/或HCK的表达受损所致。因此,我们的数据确立了NBS1蛋白作为通过SFK成员调节PI3K活性的新功能。

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