新西兰肥胖(NZO)小鼠品系NZL/Lt小鼠的2型糖尿病发病不需要抗胰岛素受体自身抗体。

Marcia F McInerney, Sonia M Najjar, Deanna Brickley, Mary Lutzke, George A Abou-Rjaily, Peter Reifsnyder, Bradford D Haskell, Kevin Flurkey, Ying-Jian Zhang, Susan L Pietropaolo, Massimo Pietropaolo, James P Byers, Edward H Leiter
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引用次数: 5

摘要

新西兰肥胖(NZO)小鼠品系与相关的新西兰黑(NZB)品系具有许多免疫表型特征。其中有高比例的B-1 B淋巴细胞,这是一种与自身抗体产生相关的亚群。大约50%的NZO/HlLt男性发展为慢性胰岛素抵抗型2型糖尿病综合征,并伴有2个不寻常的特征:富含B淋巴细胞的岛周浸润和抗胰岛素受体自身抗体(AIRAs)的发展。为了确定B淋巴细胞和AIRAs在该模型中的潜在致病作用,将NZB/BlJ背景上的一个被破坏的免疫球蛋白重链基因(Igh-6)回交4代至NZO/HlLt背景,然后进行交叉杂交,产生的小鼠最初分离为野生型和突变的Igh-6等位基因,从而可以比较综合征的发展。一项新的流式细胞分析(AIRA与转染的稳定表达小鼠胰岛素受体的中国仓鼠卵巢细胞结合)显示,Igh-6完整雄性血清中存在IgM和IgG亚类AIRAs,但在Igh-6缺失雄性血清中不存在。然而,B淋巴细胞和抗体的缺失并不能显著影响突变型与野生型男性的无糖尿病生存。高-6null的雄性比野生型的雄性体重增加的速度要慢,这可能解释了高血糖症的延迟,但不是预防。因此,慢性糖尿病患者胰岛素周围炎的AIRA和b淋巴细胞成分对胰岛素抵抗的发展或最终胰腺β细胞衰竭和损失都不是必需的。通过对高-6野生型分离株的近亲杂交,产生了一个新的菌株NZL。目前,在F10代,NZL小鼠表现出与NZO/HlLt雄性相同的青少年发病肥胖,但发生2型糖尿病的频率更高(> 80%)。此外,与难以繁殖的NZO/HlLt小鼠不同,NZL/Lt菌株繁殖良好,因此为肥胖/糖尿病研究人员提供了明显的优势。
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Anti-insulin receptor autoantibodies are not required for type 2 diabetes pathogenesis in NZL/Lt mice, a New Zealand obese (NZO)-derived mouse strain.

The New Zealand obese (NZO) mouse strain shares with the related New Zealand black (NZB) strain a number of immunophenotypic traits. Among these is a high proportion of B-1 B lymphocytes, a subset associated with autoantibody production. Approximately 50% of NZO/HlLt males develop a chronic insulin-resistant type 2 diabetes syndrome associated with 2 unusual features: the presence of B lymphocyte-enriched peri-insular infiltrates and the development of anti-insulin receptor autoantibodies (AIRAs). To establish the potential pathogenic contributions of B lymphocytes and AIRAs in this model, a disrupted immunoglobulin heavy chain gene (Igh-6) congenic on the NZB/BlJ background was backcrossed 4 generations into the NZO/HlLt background and was then intercrossed to produce mice that initially segregated for wild-type versus the mutant Igh-6 allele and thus permitted comparison of syndrome development. A new flow cytometric assay (AIRA binding to transfected Chinese hamster ovary cells stably expressing mouse insulin receptor) showed IgM and IgG subclass AIRAs in serum from Igh-6 intact males, but not in Igh-6null male serum. However, the absence of B lymphocytes and antibodies distinguishing mutant from wild-type males failed to significantly affect diabetes-free survival. The Igh-6null males gained weight less rapidly than wild-type males, probably accounting for a retardation, but not prevention, of hyperglycemia. Thus, AIRA and the B-lymphocyte component of the peri-insulitis in chronic diabetics were not essential either to development of insulin resistance or to eventual pancreatic beta cell failure and loss. A new substrain, designated NZL, was generated by inbreeding Igh-6 wild-type segregants. Currently at the F10 generation, NZL mice exhibit the same juvenile-onset obesity as NZO/HlLt males, but develop type 2 diabetes at a higher frequency (> 80%). Also, unlike NZO/HlLt mice that are difficult to breed, the NZL/Lt strain breeds well and thus offers clear advantages to obesity/diabetes researchers.

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