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与原钙黏蛋白γ相互作用可调节原钙黏蛋白α的细胞表面表达。

Interaction with protocadherin-gamma regulates the cell surface expression of protocadherin-alpha.

作者信息

Murata Yoji, Hamada Shun, Morishita Hirofumi, Mutoh Tetsuji, Yagi Takeshi

机构信息

KOKORO Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, 565-0871, Japan.

出版信息

J Biol Chem. 2004 Nov 19;279(47):49508-16. doi: 10.1074/jbc.M408771200. Epub 2004 Sep 3.

Abstract

The protocadherin-alpha (CNR/Pcdhalpha) and protocadherin-gamma (Pcdhgamma) proteins, members of the cadherin superfamily, are putative cell recognition/adhesion molecules in the brain. Overexpressed cadherins are generally expressed on the cell surface and elicit cell adhesion activity in several cell lines, although hardly any overexpressed CNR/Pcdhalpha proteins are expressed on the cell surface, except on HEK293T cells, which show low expression. We analyzed the expression of CNR/Pcdhalpha and Pcdhgamma in HEK293T cells and found that they formed a protein complex and that Pcdhgamma enhanced the surface expression of CNR/Pcdhalpha. This enhanced surface expression was confirmed by flow cytometry analysis and by marking cell surface proteins with biotin. The enhancement was observed using different combinations of CNR/Pcdhalpha and Pcdhgamma proteins. The surface expression activity was enhanced by the extracellular domains of the proteins, which could bind each other. Their cytoplasmic domains also had binding activity and influenced their localization. Their protein-protein interaction was also detected in extracts of mouse brain and two neuroblastoma cell lines. Thus, interactions between CNR/Pcdhalpha and Pcdhgamma regulate their surface expression and contribute to the combinatorial diversity of cell recognition proteins in the brain.

摘要

原钙黏蛋白α(CNR/Pcdhalpha)和原钙黏蛋白γ(Pcdhgamma)蛋白是钙黏蛋白超家族的成员,被认为是大脑中的细胞识别/黏附分子。过表达的钙黏蛋白通常在细胞表面表达,并在多种细胞系中引发细胞黏附活性,然而,除了在低表达的HEK293T细胞上,几乎没有过表达的CNR/Pcdhalpha蛋白在细胞表面表达。我们分析了CNR/Pcdhalpha和Pcdhgamma在HEK293T细胞中的表达,发现它们形成了一种蛋白质复合物,并且Pcdhgamma增强了CNR/Pcdhalpha的表面表达。通过流式细胞术分析以及用生物素标记细胞表面蛋白证实了这种增强的表面表达。使用不同组合的CNR/Pcdhalpha和Pcdhgamma蛋白均观察到了这种增强作用。蛋白质的细胞外结构域可相互结合,从而增强了表面表达活性。它们的细胞质结构域也具有结合活性并影响其定位。在小鼠脑提取物和两种神经母细胞瘤细胞系中也检测到了它们的蛋白质-蛋白质相互作用。因此,CNR/Pcdhalpha和Pcdhgamma之间的相互作用调节它们的表面表达,并有助于大脑中细胞识别蛋白的组合多样性。

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