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人β2-微球蛋白可特异性增强转染鼠细胞中HLA I类分子的细胞表面表达。

Human beta 2-microglobulin specifically enhances cell-surface expression of HLA class I molecules in transfected murine cells.

作者信息

Perarnau B M, Gillet A C, Hakem R, Barad M, Lemonnier F A

机构信息

Centre d'Immunologie Institut National de la Santé et de la Recherche Médicale, Marseille, France.

出版信息

J Immunol. 1988 Aug 15;141(4):1383-9.

PMID:2456352
Abstract

Sequential transfections of P815 murine mastocytoma cells with class I gene encoding either HLA-Cw3, HLA-A3, or HLA-B7 H chain and subsequently with a human beta 2-microglobulin gene were performed to evaluate the relative efficiency of human and murine beta 2-microglobulins in promoting the cell-surface expression of HLA-class I molecules. A 6-, 11-, and 40-fold specific enhancement of the cell-surface expression of HLA-Cw3, HLA-A3, and HLA-B7 molecules, respectively, was observed in cells co-transfected with human beta 2-microglobulin gene. This effect was attributed to a more efficient association of HLA H chains with human than with murine beta 2-microglobulin, which apparently allowed a more rapid transport of the HLA molecules from the endoplasmic reticulum to the Golgi apparatus.

摘要

对P815小鼠肥大细胞瘤细胞进行连续转染,先用编码HLA - Cw3、HLA - A3或HLA - B7重链的I类基因转染,随后用人类β2 - 微球蛋白基因转染,以评估人类和小鼠β2 - 微球蛋白在促进HLA - I类分子细胞表面表达方面的相对效率。在用人类β2 - 微球蛋白基因共转染的细胞中,分别观察到HLA - Cw3、HLA - A3和HLA - B7分子的细胞表面表达特异性增强了6倍、11倍和40倍。这种效应归因于HLA重链与人类β2 - 微球蛋白的结合比与小鼠β2 - 微球蛋白更有效,这显然使得HLA分子能更快速地从内质网转运到高尔基体。

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