SIRT1 Regulates the Inflammatory Response of Vascular Adventitial Fibroblasts through Autophagy and Related Signaling Pathway

被引:31
作者
Wang, Wei-Rong [1 ,2 ]
Li, Ting-Ting [3 ]
Jing, Ting [4 ]
Li, Yan-Xiang [4 ]
Yang, Xiao-Feng [4 ]
He, Yan-Hao [4 ]
Zhang, Wei [4 ]
Zhang, Ji-Ye [5 ]
Lin, Rong [4 ]
机构
[1] Xi An Jiao Tong Univ, Cardiovasc Res Ctr, Res Inst Atherosclerot Dis, Xian, Peoples R China
[2] Xi An Jiao Tong Univ, Hlth Sci Ctr, Lab Anim Ctr, Xian, Peoples R China
[3] Xian Chest Hosp, Dept Pharm, Xian, Peoples R China
[4] Xi An Jiao Tong Univ, Hlth Sci Ctr, Dept Pharmacol, 76 Yanta West Rd, Xian 710061, Shaanxi, Peoples R China
[5] Xi An Jiao Tong Univ, Hlth Sci Ctr, Sch Pharm, Xian, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
SIRT1; Vascular adventitial fibroblasts; Autophagy; Inflammation; Akt/mTOR; ENDOTHELIAL-CELLS; ACTIVATION; DEACETYLATION; MODULATION; EXPRESSION; APOPTOSIS; DISEASE; STRESS; INJURY;
D O I
10.1159/000457878
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: Autophagy is a lysosomal degradation pathway that is essential for cellular survival, differentiation, and homeostasis. Sirtuin 1 (SIRT1), a NAD(+) -dependent deacetylase, plays a pivotal role in modulation of autophagy. Recent studies found that autophagy was involved in the regulation of inflammatory response. In this study, we aimed to determine the effect of SIRT1 on autophagy and inflammation, and whether autophagy can regulate the inflammatory response in vascular adventitial fibroblasts (VAFs). Methods: Cell autophagy was evaluated by fluorescence microscope and transmission electron microscopy. The expression of protein and mRNA were determined by Western blot analysis and real time-PCR. The production of cytokine was detected by ELISA. Results: TNF-alpha induced autophagy and increased SIRT1 expression in VAFs. SIRT1 activator resveratrol enhanced TNF-alpha-induced VAF autophagy. In contrast, SIRT1 knockdown attenuated VAF autophagy. Both the Akt inhibitor MK2206 and mTOR inhibitor rapamycin further increased TNF-alpha-induced VAF autophagy. Furthermore. SIRT1 knockdown increased Akt phosphorylation and inhibited the autophagy in VAFs. However, MK2206 attenuated the effect of SIRT1 knockdown on VAF autophagy. In addition, ingenuity pathway analysis showed that there is a relationship between cell autophagy and inflammation. We found that SIRT1 knockdown increased the expression of NLRP3 and interleukin (IL)-6 and promoted the production of IL-1 beta in VAFs. Further study showed that autophagy activation decreased the expression of NLRP3 and IL-6 and inhibited the production of IL-1 beta, whereas autophagy inhibition increased the inflammatory response of VAFs. More importantly, our study showed that autophagy was involved in the degradation of NLRP3 through the autophagy-lysosome pathway. Conclusion: SIRT1 not only regulates VAF autophagy through the Akt/mTOR signaling pathway but also suppresses the inflammatory (C) 2017 The Author(s) response of VAFs through autophagy. Published by S. Karger AG, Basel
引用
收藏
页码:569 / 582
页数:14
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