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Shp2参与海马前体细胞的神经元分化。

Shp2 is involved in neuronal differentiation of hippocampal precursor cells.

作者信息

Kim Hak-Jae, Han Ah Mi, Shim Jae Hwan, Yoon Hye Hyun, Kwon Hyockman, Kwon Yunhee Kim

机构信息

Department of Biology, Kyunghee University, Dongdaemun-Gu, Seoul 130-701, Korea.

出版信息

Arch Pharm Res. 2007 Jun;30(6):750-4. doi: 10.1007/BF02977638.

Abstract

HiB5 is a multipotent hippocampal stem cell line whose differentiation into cells of a neuronal phenotype is promoted by neurotrophic factors such as PDGF and brain-derived neurotrophic factor (BDNF). We examined the potential role of Src homology 2 (SH2)-containing protein tyrosine phosphatase (Shp2) in this differentiation process. We found that Shp2 became tyrosine phosphorylated following PDGF treatment. Wild-type Shp2 enhanced the expression of neurofilament, synapsin I and PSD95 by PDGF and BDNF, whereas their expression was attenuated by the catalytically inactive mutants Shp2C/S and Shp2DeltaP. Formation of dendritic spine-like structures increased with wild-type Shp2, but diminished with Shp2C/S and Shp2DeltaP. PSD95, localized in the post-synaptic density region of dendritic spines, PDGFRbeta and TrkB were co-immunoprecipitated with Shp2 antibodies. These results suggest that Shp2 plays a positive role in mediating PDGF- and BDNF-activated signaling which promotes the formation of dendritic spines.

摘要

HiB5是一种多能海马干细胞系,其向神经元表型细胞的分化受到诸如血小板衍生生长因子(PDGF)和脑源性神经营养因子(BDNF)等神经营养因子的促进。我们研究了含Src同源2(SH2)结构域的蛋白酪氨酸磷酸酶(Shp2)在这一分化过程中的潜在作用。我们发现,PDGF处理后Shp2发生酪氨酸磷酸化。野生型Shp2增强了PDGF和BDNF诱导的神经丝、突触素I和PSD95的表达,而其表达在催化失活的突变体Shp2C/S和Shp2DeltaP作用下减弱。野生型Shp2使树突棘样结构的形成增加,但Shp2C/S和Shp2DeltaP使其减少。定位于树突棘突触后致密区的PSD95、PDGFRβ和TrkB与Shp2抗体进行了共免疫沉淀。这些结果表明,Shp2在介导PDGF和BDNF激活的信号传导中起积极作用,该信号传导促进树突棘的形成。

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