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晚期糖基化终产物受体(RAGE)在神经元分化中的作用。

The role of receptor for advanced glycation end products (RAGE) in neuronal differentiation.

机构信息

Department of Anatomy with Radiology, Centre for Brain Research, Faculty of Medical and Health Science, University of Auckland, Auckland, New Zealand.

出版信息

J Neurosci Res. 2012 Jun;90(6):1136-47. doi: 10.1002/jnr.23014. Epub 2012 Feb 16.

Abstract

The receptor for advanced glycation end products (RAGE) is a multiligand receptor protein thought to play an important role in neuronal differentiation. RAGE can bind a number of ligands and activate a variety of signalling pathways that lead to diverse downstream effects. Amphoterin and S100B are endogenous ligands, the interaction of which with RAGE is known to be involved in defined physiological processes. The present study investigated the spatiotemporal pattern of the expression for RAGE and its ligands, amphoterin and S100B, during neuronal differentiation of NT2/D1 cells. In this study, all three proteins were shown to increase with progression of neuronal differentiation as determined by Western blotting, raising the possibility that both amphoterin and S100B may interact with RAGE and have important functions during the process of cell differentiation. Moreover, blocking the activation of RAGE with neutralizing antibody in the presence of retinoic acid disrupted the progression of normal neuronal differentiation. Immunocytochemistry (ICC) studies showed that amphoterin partially colocalized with RAGE within differentiating NT2 cells, whereas S100B showed a high degree of colocalization. This result suggests that S100B is more likely to be the principal ligand for RAGE during the differentiation process and that RAGE and amphoterin might have both independent and combined roles. Moreover, RAGE was expressed only in cells that were committed to a neuronal phenotype, suggesting direct involvement of RAGE in mediating cellular changes within differentiating neuronal cells. Further detailed studies are now required to characterize fully the role of RAGE during the neuronal differentiation period.

摘要

晚期糖基化终产物受体(RAGE)是一种多配体受体蛋白,被认为在神经元分化中发挥重要作用。RAGE 可以结合许多配体并激活多种信号通路,从而导致不同的下游效应。两性蛋白和 S100B 是内源性配体,已知它们与 RAGE 的相互作用参与了特定的生理过程。本研究调查了 RAGE 及其配体两性蛋白和 S100B 在 NT2/D1 细胞神经元分化过程中的时空表达模式。在这项研究中,通过 Western blot 确定,所有三种蛋白都随着神经元分化的进展而增加,这表明两性蛋白和 S100B 可能与 RAGE 相互作用,并在细胞分化过程中具有重要功能。此外,在用维甲酸存在的情况下用中和抗体阻断 RAGE 的激活会破坏正常神经元分化的进展。免疫细胞化学(ICC)研究表明,在分化的 NT2 细胞中,两性蛋白部分与 RAGE 共定位,而 S100B 则高度共定位。这一结果表明,在分化过程中,S100B 更有可能是 RAGE 的主要配体,而 RAGE 和两性蛋白可能具有独立和联合的作用。此外,RAGE 仅在向神经元表型分化的细胞中表达,这表明 RAGE 直接参与介导分化神经元细胞内的细胞变化。现在需要进行更详细的研究,以充分表征 RAGE 在神经元分化期间的作用。

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