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β细胞破坏起始的自身免疫研究。X. 糖尿病易感性BB大鼠中,在胰岛炎和糖尿病之前出现的一种膜结合胰岛细胞特异性38 kDa自身抗原的延迟表达。

Studies on autoimmunity for initiation of beta-cell destruction. X. Delayed expression of a membrane-bound islet cell-specific 38 kDa autoantigen that precedes insulitis and diabetes in the diabetes-prone BB rat.

作者信息

Ko I Y, Jun H S, Kim G S, Yoon J W

机构信息

Laboratory of Viral and Immunopathogenesis of Diabetes, University of Calgary, Alberta, Canada.

出版信息

Diabetologia. 1994 May;37(5):460-5. doi: 10.1007/s001250050132.

Abstract

The diabetic syndrome in the DP-BB rat results from progressive beta-cell destruction by autoimmune responses. However, the initial events causing the autoimmune destruction of beta cells remain largely unknown. Our recent experimental results suggest that the delayed expression of a beta-cell-specific autoantigen may result in the initiation of beta-cell-specific autoimmunity. The present investigation was initiated to identify such an autoantigen. Islets were isolated from DP-BB rats of several different ages, and protein extracts from the membrane fraction of the islet preparations were immunoprecipitated with sera from diabetic DP-BB rats. We have found that a membrane-bound islet cell-specific 38 kDa autoantigen is not expressed early in the life of DP-BB rats, but is delayed-expressed by approximately 30 days of age, the time at which immunological effectors begin to recognize beta cells. In contrast, a 64 kDa islet cell protein is expressed from birth in DP-BB rats. On the basis of these observations, we suggest that delayed expression of a gene encoding for the membrane-bound islet cell-specific 38 kDa autoantigen may result in a breakdown of self-tolerance, leading to beta-cell-specific autoimmune IDDM in the BB rat.

摘要

DP - BB大鼠的糖尿病综合征是由自身免疫反应导致的胰岛β细胞进行性破坏引起的。然而,引发β细胞自身免疫破坏的初始事件在很大程度上仍不清楚。我们最近的实验结果表明,一种β细胞特异性自身抗原的延迟表达可能导致β细胞特异性自身免疫的启动。本研究旨在鉴定这样一种自身抗原。从几只不同年龄的DP - BB大鼠中分离胰岛,并用糖尿病DP - BB大鼠的血清对胰岛制备物膜部分的蛋白质提取物进行免疫沉淀。我们发现,一种与膜结合的胰岛细胞特异性38 kDa自身抗原在DP - BB大鼠生命早期不表达,而是在大约30日龄时延迟表达,此时免疫效应器开始识别β细胞。相比之下,一种64 kDa的胰岛细胞蛋白在DP - BB大鼠出生时就已表达。基于这些观察结果,我们认为编码与膜结合的胰岛细胞特异性38 kDa自身抗原的基因的延迟表达可能导致自身耐受性的破坏,从而在BB大鼠中引发β细胞特异性自身免疫性胰岛素依赖型糖尿病。

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