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Blimp-1 inhibits Th9 cell differentiation and attenuates diabetic coronary heart disease.

Abstract
Diabetic coronary heart disease (DM-CHD) poses a major threat to the world. The newly described T cell subset-Th9 cells and related cytokine interleukin (IL)-9 play important roles in the pathogenesis of diabetes and atherosclerosis. B lymphocyte-induced maturation protein 1 (Blimp-1) has been indicated to negatively regulate Th9 development in allergic asthma, but its role in DM-CHD remains unclear. Hence, this study was designed to investigate the role of Blimp-1 in DM-CHD and to elucidate whether the mechanism was associated with regulation of Th9 cell differentiation. Our results showed that serum Blimp-1 mRNA level was decreased whereas proportion of Th9 cells (IL-9+ CD4+ T cells) and serum level of Th9-related IL-9 were increased in DM-CHD patients. Furthermore, serum Blimp-1 mRNA level was negatively correlated with IL-9 level in DM-CHD patients. Importantly, administration of lentiviruses expressing Blimp-1 (LV-Blimp-1) significantly inhibited Th9 cell differentiation and alleviated the severity of atherosclerotic lesions in the aorta and coronary artery, dyslipidemia, inflammation, vascular endothelial dysfunction, and oxidative stress in DM-CHD model rats. Collectively, Blimp-1 exerts a protective effect in DM-CHD rats and the mechanism might involve inhibition of Th9 cell differentiation.
AuthorsHaiyan Chen, Fangyuan Gao, Yi Bao, Jiaoyang Zheng, Liangliang Sun, Wei Tang, Junjie Zou, Yongquan Shi
JournalInternational immunopharmacology (Int Immunopharmacol) Vol. 95 Pg. 107510 (Jun 2021) ISSN: 1878-1705 [Electronic] Netherlands
PMID33706054 (Publication Type: Journal Article)
CopyrightCopyright © 2021. Published by Elsevier B.V.
Chemical References
  • Interleukin-9
  • Positive Regulatory Domain I-Binding Factor 1
Topics
  • Adult
  • Aged
  • Animals
  • Cell Differentiation
  • Coronary Disease (immunology)
  • Diabetes Mellitus, Type 2 (immunology)
  • Female
  • Humans
  • Interleukin-9 (immunology)
  • Male
  • Middle Aged
  • Positive Regulatory Domain I-Binding Factor 1 (genetics, immunology)
  • Rats, Sprague-Dawley
  • T-Lymphocyte Subsets (immunology)
  • Rats

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