Nucleotide-binding oligomerization domain-containing protein 2 (Nod2) modulates T1DM susceptibility by gut microbiota

被引:23
|
作者
Li, Yang-yang [1 ,2 ]
Pearson, James A. [1 ]
Chao, Chen [1 ,3 ]
Peng, Jian [1 ]
Zhang, Xiaojun [1 ]
Zhou, Zhiguang [3 ]
Liu, Yu [2 ,4 ]
Wong, F. Susan [5 ]
Wen, Li [1 ,3 ]
机构
[1] Yale Univ, Sch Med, Endocrinol Sect, 333 Cedar St, New Haven, CT 06519 USA
[2] Jilin Univ, Hosp 2, Dept Endocrinol, Changchun 130041, Jilin, Peoples R China
[3] Cent S Univ, Xiangya Hosp 2, Dept Metab & Endocrinol, Key Lab Diabet Immunol, Changsha 410011, Hunan, Peoples R China
[4] Nanjing Med Univ, Sir Run Run Shaw Hosp, Dept Endocrinol, Nanjing 211100, Jiangsu, Peoples R China
[5] Cardiff Univ, Sch Med, Div Infect & Immun, Diabet Res Grp, Cardiff CF14 4XN, S Glam, Wales
关键词
Type 1 diabetes mellitus; NOD; Nod2; Innate immunity; Gut microbiota; CD103(+) DENDRITIC CELLS; PANCREATIC LYMPH-NODES; BACTERIAL-ANTIGENS; ADAPTIVE IMMUNITY; IMMUNOGLOBULIN-A; SMALL-INTESTINE; CROHNS-DISEASE; T-CELLS; MICE; CHILDHOOD;
D O I
10.1016/j.jaut.2017.05.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nucleotide-binding oligomerization domain-containing protein 2 (Nod2) is an innate immune receptor. To investigate the role of Nod2 in susceptibility to the autoimmune disease, type 1 diabetes mellitus (T1DM), we generated Nod2(-/-) non-obese diabetic (NOD) mice. The Nod2(-/-)NOD mice had different composition of the gut microbiota compared to Nod2(+/+)NOD mice and were significantly protected from diabetes, but only when housed separately from Nod2(+/+) NOD mice. This suggested that T1DM susceptibility in Nod2(-/-)NOD mice is dependent on the alteration of gut microbiota, which modulated the frequency and function of IgA-secreting B-cells and IL-10 promoting T-regulatory cells. Finally, colonizing germ-free NOD mice with Nod2(-/-)NOD gut microbiota significantly reduced pro-inflammatory cytokinesecreting immune cells but increased T-regulatory cells. Thus, gut microbiota modulate the immune system and T1D susceptibility. Importantly, our study raises a critical question about the housing mode in the interpretation of the disease phenotype of genetically-modified mouse strains in T1DM studies. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:85 / 95
页数:11
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