Abstract |
Interleukin 17 (IL-17) plays an important role in the pathogenesis of cardiac interstitial fibrosis. In this study, we explored the role of interleukin-17 in the development of diabetic cardiomyopathy and the underlying mechanisms. The level of IL-17 increased in both the serum and cardiac tissue of diabetic mice. Knockout of IL-17 improved cardiac function of diabetic mice induced by streptozotocin (STZ), and significantly alleviated interstitial fibrosis as manifested by reduced collagen mRNA expression and collagen deposition evaluated by Masson's staining. High glucose treatment induced collagen production were abolished in cultured IL-17 knockout cardiac fibroblasts (CFs). The levels of long noncoding RNA-AK081284 were increased in the CFs treated with high glucose or IL-17. Knockout of IL-17 abrogated high glucose induced upregulation of AK081284. Overexpression of AK081284 in cultured CFs promoted the production of collagen and TGFβ1. Both high glucose and IL-17 induced collagen and TGFβ1 production were mitigated by the application of the siRNA for AK081284. In summary, deletion of IL-17 is able to mitigate myocardial fibrosis and improve cardiac function of diabetic mice. The IL-17/AK081284/TGFβ1 signaling pathway mediates high glucose induced collagen production. This study indicates the therapeutic potential of IL-17 inhibition on diabetic cardiomyopathy disease associated with fibrosis.
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Authors | Yang Zhang, Yi-Yuan Zhang, Ting-Ting Li, Jin Wang, Yuan Jiang, Yue Zhao, Xue-Xin Jin, Gen-Long Xue, Ying Yang, Xiao-Fang Zhang, Yang-Yang Sun, Zhi-Ren Zhang, Xu Gao, Zhi-Min Du, Yan-Jie Lu, Bao-Feng Yang, Zhen-Wei Pan |
Journal | Journal of molecular and cellular cardiology
(J Mol Cell Cardiol)
Vol. 115
Pg. 64-72
(02 2018)
ISSN: 1095-8584 [Electronic] England |
PMID | 29305939
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2018. Published by Elsevier Ltd. |
Chemical References |
- Interleukin-17
- RNA, Long Noncoding
- Collagen
- Glucose
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Topics |
- Animals
- Cell Proliferation
- Cells, Cultured
- Collagen
(metabolism)
- Diabetes Mellitus, Experimental
(blood, diagnostic imaging, genetics, physiopathology)
- Fibroblasts
(metabolism, pathology)
- Fibrosis
- Glucose
(toxicity)
- Heart Function Tests
- Interleukin-17
(blood, metabolism)
- Male
- Mice, Inbred C57BL
- Mice, Knockout
- Myocardium
(metabolism, pathology)
- RNA, Long Noncoding
(metabolism)
- Up-Regulation
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