1. Sirt6 regulates autophagy in AGE-treated endothelial cells via KLF4
- Author
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Jing Tong, Bing Ji, Yan-Hua Gao, Hao Lin, Fan Ping, Fei Chen, and Xue-Bo Liu
- Subjects
Kruppel-Like Factor 4 ,Mice ,Nutrition and Dietetics ,Endocrinology, Diabetes and Metabolism ,Autophagy ,Animals ,Endothelial Cells ,Sirtuins ,Medicine (miscellaneous) ,Endothelium ,Cardiology and Cardiovascular Medicine ,Diabetes Mellitus, Experimental - Abstract
High glucose and its byproducts are important factors causing dysfunction of endothelial cells. Autophagy is critical for endothelial cellular homeostasis. However, the specific molecular mechanism of how autophagy is regulated in endothelial cells under high-glucose condition remains unknown. We aim to explore the role Sirt6 plays in regulating autophagy in AGE-treated endothelial cells and how this function is exerted via KLF4.Our results indicate that autophagy level increased in AGE-treated endothelial cells alongside with higher Sirt6 and KLF4 expression level. What's more, knock-in of Sirt6 by adenovirus led to augmented autophagy level while knockdown of Sirt6 led to the opposite. We also verified that Sirt6 affected KLF4 expression positively but KLF4 didn't influence Sirt6 expression level while knocking out of KLF4 impaired Sirt6-enhanced autophagy. Finally we found that STZ-induced diabetic mice showed more autophagosomes in endothelium and Sirt6 knockdown by adeno-associated virus reduced the number of autophagosomes. Knockdown of Sirt6 also caused impaired endothelium integrity but echocardiography indicated there were no significant functional differences.Our research reveals more about how Sirt6 regulates autophagy in endothelial cells under high-glucose simulated condition and provides further insight into the relationships between Sirt6 and KLF4.
- Published
- 2022
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