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在非肥胖糖尿病(NOD)小鼠自身免疫性糖尿病进展过程中,会产生抵抗免疫攻击的β细胞。

β Cells that Resist Immunological Attack Develop during Progression of Autoimmune Diabetes in NOD Mice.

作者信息

Rui Jinxiu, Deng Songyan, Arazi Arnon, Perdigoto Ana Luisa, Liu Zongzhi, Herold Kevan C

机构信息

Department of Immunobiology, Yale University, New Haven, CT 06520, USA.

Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, MA 02142, USA.

出版信息

Cell Metab. 2017 Mar 7;25(3):727-738. doi: 10.1016/j.cmet.2017.01.005. Epub 2017 Feb 9.

Abstract

Type 1 diabetes (T1D) is a chronic autoimmune disease that involves immune-mediated destruction of β cells. How β cells respond to immune attack is unknown. We identified a population of β cells during the progression of T1D in non-obese diabetic (NOD) mice that survives immune attack. This population develops from normal β cells confronted with islet infiltrates. Pathways involving cell movement, growth and proliferation, immune responses, and cell death and survival are activated in these cells. There is reduced expression of β cell identity genes and diabetes antigens and increased immune inhibitory markers and stemness genes. This new subpopulation is resistant to killing when diabetes is precipitated with cyclophosphamide. Human β cells show similar changes when cultured with immune cells. These changes may account for the chronicity of the disease and the long-term survival of β cells in some patients.

摘要

1型糖尿病(T1D)是一种慢性自身免疫性疾病,涉及免疫介导的β细胞破坏。β细胞如何应对免疫攻击尚不清楚。我们在非肥胖糖尿病(NOD)小鼠的T1D进展过程中鉴定出一群在免疫攻击中存活下来的β细胞。这群细胞由面对胰岛浸润的正常β细胞发育而来。涉及细胞运动、生长和增殖、免疫反应以及细胞死亡和存活的信号通路在这些细胞中被激活。β细胞身份基因和糖尿病抗原的表达降低,免疫抑制标志物和干性基因的表达增加。当用环磷酰胺诱发糖尿病时,这个新的亚群对杀伤具有抗性。人β细胞与免疫细胞共培养时也表现出类似变化。这些变化可能解释了该疾病的慢性病程以及某些患者中β细胞的长期存活。

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