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Src 样衔接蛋白(Slap)是有丝分裂原的负调控因子。

Src-like adaptor protein (Slap) is a negative regulator of mitogenesis.

作者信息

Roche S, Alonso G, Kazlauskas A, Dixit V M, Courtneidge S A, Pandey A

机构信息

CNRS EP612, Faculté de Pharmacie, Montpellier, France.

出版信息

Curr Biol. 1998 Aug 27;8(17):975-8. doi: 10.1016/s0960-9822(98)70400-2.

Abstract

The Src-like adaptor protein (Slap) is a recently identified adaptor protein containing Src homology 3 (SH3) and SH2 domains. Slap is found in a wide range of cell types and was shown to interact with the Eck receptor tyrosine kinase in a yeast two-hybrid interaction screen [1]. Here, we found that Slap is expressed in NIH3T3 cells and could associate with the activated platelet-derived growth factor (PDGF) receptor. Using mutated versions of the PDGF receptor and phosphopeptide competition experiments, we determined that Slap has the highest affinity for the Src-binding site of the PDGF receptor. Our inability to produce cell lines that stably expressed Slap suggested that Slap inhibited cell growth. We further investigated this issue by transiently expressing Slap by microinjection. Overexpression of Slap by this method inhibited DNA synthesis induced by PDGF and serum, whereas overexpression of the adaptor proteins Grb2 and Shc did not. Finally, microinjection of a Slap antibody into NIH3T3 cells that had been stimulated with suboptimal doses of growth factors potentiated the effects of the growth factors. These data suggest that, unlike other adaptor proteins, Slap is a negative regulator of signalling initiated by growth factors.

摘要

Src 样衔接蛋白(Slap)是一种最近鉴定出的含有Src同源结构域3(SH3)和SH2结构域的衔接蛋白。Slap存在于多种细胞类型中,并且在酵母双杂交相互作用筛选中显示与Eck受体酪氨酸激酶相互作用[1]。在此,我们发现Slap在NIH3T3细胞中表达,并且能够与活化的血小板衍生生长因子(PDGF)受体结合。通过使用PDGF受体的突变体和磷酸肽竞争实验,我们确定Slap对PDGF受体的Src结合位点具有最高亲和力。我们无法产生稳定表达Slap的细胞系,这表明Slap抑制细胞生长。我们通过显微注射瞬时表达Slap进一步研究了这个问题。通过这种方法过表达Slap抑制了PDGF和血清诱导的DNA合成,而衔接蛋白Grb2和Shc的过表达则没有。最后,将Slap抗体显微注射到用次优剂量生长因子刺激的NIH3T3细胞中,增强了生长因子的作用。这些数据表明,与其他衔接蛋白不同,Slap是生长因子引发信号传导的负调节因子。

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