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首页> 外文期刊>Molecular and Cellular Endocrinology >Leptin promotes the tyrosine phosphorylation of SHC proteins and SHC association with GRB2.
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Leptin promotes the tyrosine phosphorylation of SHC proteins and SHC association with GRB2.

机译:瘦蛋白促进SHC蛋白的酪氨酸磷酸化以及SHC与GRB2的缔合。

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摘要

The identification and characterization of proteins that become tyrosine phosphorylated in response to growth factor stimulation is critical for furthering our understanding of the signal transduction pathways involved in the regulation of cell proliferation, differentiation as well as metabolic activities. In this report, we demonstrate for the first time, that leptin is able to induce the tyrosine phosphorylation of the SH(2) containing protein SHC. These studies have been carried out on a human embryonic cell line (HEK 293) transfected with the cDNA encoding for the long form of the leptin receptor and stably expressing the receptor itself. We also shown that upon tyrosine phosphorylation, SHC associated with the adaptor protein, Grb(2). The formation of this complex may directly link tyrosine phosphorylation events to Ras activation and may be a critical step in proliferation and/or differentiation of cells. In conclusion, these results indicate that leptin receptor, after binding the ligand, activates several pathways for signal transduction that might lead to mitogenic effect.
机译:酪氨酸响应生长因子刺激而被磷酸化的蛋白质的鉴定和表征,对于进一步增进我们对涉及细胞增殖,分化以及代谢活性调节的信号转导途径的理解至关重要。在此报告中,我们首次证明,瘦素能够诱导SH(2)包含蛋白SHC的酪氨酸磷酸化。这些研究已在人类胚胎细胞系(HEK 293)上进行,该细胞系已被编码长形式的瘦素受体并稳定表达该受体本身的cDNA转染。我们还显示,酪氨酸磷酸化后,SHC与衔接蛋白Grb(2)相关。该复合物的形成可以直接将酪氨酸磷酸化事件与Ras活化联系起来,并且可能是细胞增殖和/或分化的关键步骤。总之,这些结果表明,瘦素受体在结合配体后激活了信号转导的几种途径,这可能导致促有丝分裂作用。

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