[Gly14]-humanin restores cathepsin D function via FPRL1 and promotes autophagic degradation of Ox-LDL in HUVECs

被引：9

作者：

Ding, Yu ^{[1
,2
]}

Feng, Yue ^{[1
]}

Zou, Yutian ^{[1
]}

Wang, Fen ^{[2
]}

Liu, Huihui ^{[1
]}

Liu, Chunfeng ^{[1
,2
]}

Zhang, Yanlin ^{[1
]}

机构：

[1] Soochow Univ, Dept Neurol, Affiliated Hosp 2, Suzhou 215004, Peoples R China

[2] Soochow Univ, Inst Neurosci, Suzhou 215123, Peoples R China

来源：

NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES | 2020年 / 30卷 / 12期

基金：

中国国家自然科学基金;

关键词：

HNG; Ox-LDL; HUVECs; Cathepsin D; Atherosclerosis; FPRL1; LOW-DENSITY-LIPOPROTEIN; RESCUE FACTOR HUMANIN; ENDOTHELIAL DYSFUNCTION; CELLS; NEUROPROTECTION; RECEPTOR; PROTECTS; INJURY;

D O I：

10.1016/j.numecd.2020.07.022

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Background and aim: Abnormal aggregation of oxidized low-density lipoprotein (OxLDL) in vascular endothelial cells (VECs) is one of the major pathological changes in atherosclerotic lesions. Our research aimed to assess the mechanism of humanin (HN) in promoting autophagic degradation of Ox-LDL in HUVECs. Methods and results: Flow cytometry and lipid quantitation results showed that Ox-LDL caused lipid and cholesterol accumulation in HUVECs. Western blot results showed that Ox-LDL increased the expression of autophagy-related proteins P62 and LC3-II in a concentrationdependent manner. The cathepsin D activity assay showed that Ox-LDL inhibited the function of cathepsin D. HNG pretreatment reduced lipid and cholesterol aggregation in HUVECs induced by Ox-LDL, increased LC3-II protein level, decreased P62 protein content, and reversed Ox-LDLinduced cathepsin D functional impairment. Inhibition of the FPRL1 pathway by FPRL1 siRNA or the FPRL1-specific inhibitor Boc-MLF blocked all HNG's protective effects. These results indicate that HNG could restore cathepsin D activity and protein level in HUVECs to repair lysosomal functional damage induced by Ox-LDL, further repairing Ox-LDL-induced autophagic damage in HUVECs. Conclusion: HNG restores the activity of Ox-LDL-induced damaged lysosomal enzyme cathepsin D through its membrane protein receptor FPRL1 to promote autophagic degradation of Ox-LDL in HUVECs. (C) 2020 The Italian Diabetes Society, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.

引用

页码：2406 / 2416

页数：11