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细胞毒性T淋巴细胞相关抗原4基因敲除(CTLA-4-/-)小鼠表现出T细胞凋亡抗性,类似于自身免疫易感的非肥胖糖尿病(NOD)小鼠的情况。

CTLA-4-/- mice display T cell-apoptosis resistance resembling that ascribed to autoimmune-prone non-obese diabetic (NOD) mice.

作者信息

Bergman M L, Cilio C M, Penha-Gonçalves C, Lamhamedi-Cherradi S E, Löfgren A, Colucci F, Lejon K, Garchon H J, Holmberg D

机构信息

Department of Cell and Molecular Biology, University of Umeå, S-901 87 Umeå Sweden.

出版信息

J Autoimmun. 2001 Mar;16(2):105-13. doi: 10.1006/jaut.2000.0474.

Abstract

The genes conferring susceptibility to autoimmune (insulin-dependent) diabetes mellitus (IDDM) are, in most cases, not defined. Among the loci so far identified as associated with murine IDDM (Idd1-19), only the nature of Idd1 has been assessed. Here we show that thymocytes and peripheral lymphocytes of the non-obese diabetic (NOD) mouse are relatively resistant to apoptosis induced by gamma-irradiation. By linkage analysis of F2 progeny mice, we map this trait to a locus on chromosome 1 containing the Idd5 diabetes susceptibility region. By the use of congenic mice, we confirm the linkage data and map this locus to a 6 cM region on proximal chromosome 1. Ctla4, being localized in this chromosomal region and mediating crucial functions in T cell biology, is a logical candidate gene in the Idd5 susceptibility region. In line with this, we demonstrate that T cells from Ctla4(-/-)deficient mice show a similar resistance to gamma-irradiation-induced apoptosis as observed in the NOD mice. This reinforces the notion that CTLA-4 contributes to the pathogenesis of autoimmune diabetes.

摘要

在大多数情况下,赋予自身免疫性(胰岛素依赖型)糖尿病(IDDM)易感性的基因尚未明确。在迄今已确定与小鼠IDDM相关的基因座(Idd1 - 19)中,仅对Idd1的性质进行了评估。在此我们表明,非肥胖糖尿病(NOD)小鼠的胸腺细胞和外周淋巴细胞对γ射线诱导的凋亡具有相对抗性。通过对F2代子代小鼠进行连锁分析,我们将此性状定位到1号染色体上包含Idd5糖尿病易感区域的一个基因座。通过使用近交系小鼠,我们证实了连锁数据,并将此基因座定位到近端1号染色体上的一个6 cM区域。Ctla4位于该染色体区域并在T细胞生物学中发挥关键作用,是Idd5易感区域中一个合理的候选基因。与此一致的是,我们证明来自Ctla4(-/-)缺陷小鼠的T细胞对γ射线诱导的凋亡表现出与NOD小鼠中观察到的类似抗性。这强化了CTLA - 4参与自身免疫性糖尿病发病机制的观点。

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