Paeoniflorin protects NOD mice from T1D through regulating gut microbiota and TLR4 mediated myD88/TRIF pathway

被引:7
作者
Luo, Cheng [4 ]
Yang, Danyi [5 ,6 ]
Hou, Can [1 ,2 ,3 ]
Tan, Tingting [7 ]
Chao, Chen [1 ,2 ,3 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Metab & Endocrinol, 139 Renmin Rd, Changsha 410011, Hunan, Peoples R China
[2] Natl Clin Res Ctr Metab Dis, Changsha 410011, Hunan, Peoples R China
[3] Cent South Univ, Key Lab Diabet Immunol, Minist Educ, Changsha 410011, Hunan, Peoples R China
[4] Cent South Univ, Xiangya Hosp 2, Dept Cardiovasc Surg, Changsha 410011, Hunan, Peoples R China
[5] Cent South Univ, Xiangya Hosp 2, Dept Nephrol, Changsha 410011, Hunan, Peoples R China
[6] Cent South Univ, Xiangya Hosp 2, Hunan Key Lab Kidney Dis & Blood, Changsha 410011, Hunan, Peoples R China
[7] Cent South Univ, Sch Basic Med Sci, Dept Immunol, Changsha 410008, Hunan, Peoples R China
关键词
Type 1 diabetes mellitus; Paeoniflorin; NOD mice; Gut microbiota; TLR4; myD88; TRIF; T-CELLS; TYPE-1; INFLAMMATION; DESTRUCTION; SUPPRESSION; PREVENTS; KNOCKOUT; HUMANS;
D O I
10.1016/j.yexcr.2022.113429
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study aimed to explore the effect of PF in regulating the progression of T1D through regulating gut microbiota and inhibiting TLR4-myD88/TRIF pathway. T1D mouse models were established and received PF treatment through intraperitoneal injection. The glucose, sugar tolerance, the incidence of T1D and H&E staining were detected to verify the effect of PF on T1D. Meanwhile, the changes of gut microbiota and the permeability of intestines in mice were also measured. On parallel, the number and function of immune cells were detected by Flow Cytometry. The expressions of ZO-1, ZO-2 and TLR4-myD88/TRIF pathway related proteins were detected by western blotting. Mice received PF treatment had decreased incidence of T1D and inflammatory infiltration in islet tissues compared with those received PBS treatment. In addition to that, PF treated mice had increased Sutterella species and decreased intestinal permeability, in which the decreased ratio of Th1/Th17 and increased Treg cells were also identified. The expression of TLR4-myD88/TRIF pathway was also suppressed in response to PF treatment. Moreover, further treatment with TLR4 agonist, LPS, could reverse the effect of PF on T1D mice. PF can suppress the TLR4 mediated myD88/TRIF pathway to change the distribution of gut microbiota, so as to protect NOD mice from T1D.
引用
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页数:9
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