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胰岛中白细胞介素12信使核糖核酸的表达与非肥胖糖尿病小鼠的β细胞破坏相关。

Interleukin 12 mRNA expression in islets correlates with beta-cell destruction in NOD mice.

作者信息

Rabinovitch A, Suarez-Pinzon W L, Sorensen O

机构信息

Department of Medicine, University of Alberta, Edmonton, Canada.

出版信息

J Autoimmun. 1996 Oct;9(5):645-51. doi: 10.1006/jaut.1996.0084.

Abstract

Interferon-gamma (IFN-gamma) is implicated as a mediator of islet beta-cell destruction in autoimmune, insulin-dependent diabetes mellitus (IDDM). Because interleukin 12 (IL-12) is a potent inducer of IFN-gamma production, we sought evidence implicating IL-12 in IDDM development. In the present study, we used a reverse transcriptase polymerase chain reaction (RT-PCR) assay to measure IL-12 mRNA expression levels in islets from nonobese diabetic (NOD) mice. Expression of mRNA encoding the p40 chain of IL-12 (IL-12 p40) in mono-nuclear leukocytes isolated from islets of female NOD mice increased progressively from age 5 weeks to diabetes onset (> 13 weeks). By contrast, IL-12 p40 mRNA levels were significantly decreased in islet mononuclear leukocytes, but not spleens, from female NOD mice protected from diabetes by administration of complete Freund's adjuvant (CFA) in early life. In addition, mRNA levels of IL-12 p40, IFN-gamma and IL-2 were significantly decreased in syngeneic islet grafts, but not spleens, from female NOD mice protected from diabetes recurrence by CFA administration at the time of islet transplantation. These findings show that IL-12 gene expression in the insulitis lesion correlates with both primary and recurrent diabetes development in NOD mice, possibly via induction of T helper (Th) 1-type cytokines, IL-2 and IFN-gamma.

摘要

干扰素-γ(IFN-γ)被认为是自身免疫性胰岛素依赖型糖尿病(IDDM)中胰岛β细胞破坏的介质。由于白细胞介素12(IL-12)是IFN-γ产生的强效诱导剂,我们寻找了与IDDM发病相关的IL-12的证据。在本研究中,我们使用逆转录聚合酶链反应(RT-PCR)测定法来测量非肥胖糖尿病(NOD)小鼠胰岛中IL-12 mRNA的表达水平。从雌性NOD小鼠胰岛中分离出的单核白细胞中,编码IL-12 p40链的mRNA表达从5周龄到糖尿病发病(>13周龄)逐渐增加。相比之下,在幼年时通过给予完全弗氏佐剂(CFA)而免受糖尿病影响的雌性NOD小鼠的胰岛单核白细胞中,IL-12 p40 mRNA水平显著降低,但脾脏中未降低。此外,在胰岛移植时通过CFA给药而免受糖尿病复发影响的雌性NOD小鼠的同基因胰岛移植中,IL-12 p40、IFN-γ和IL-2的mRNA水平显著降低,但脾脏中未降低。这些发现表明,胰岛炎病变中的IL-12基因表达与NOD小鼠原发性和复发性糖尿病的发展相关,可能是通过诱导T辅助(Th)1型细胞因子IL-2和IFN-γ实现的。

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