EDIL3/Del-1 prevents aortic dissection through enhancing internalization and degradation of apoptotic vascular smooth muscle cells

被引:6
作者
Yin, Zheng [1 ,2 ,3 ,4 ]
Zhang, Jishou [1 ,2 ,3 ,4 ]
Zhao, Mengmeng [1 ,2 ,3 ,4 ]
Liu, Jianfang [1 ,2 ,3 ,4 ]
Xu, Yao [1 ,2 ,3 ,4 ]
Peng, Shanshan [1 ,2 ,3 ,4 ]
Pan, Wei [1 ,2 ,3 ,4 ]
Wei, Cheng [1 ,2 ,3 ,4 ]
Zheng, Zihui [1 ,2 ,3 ,4 ]
Liu, Siqi [1 ,2 ,3 ,4 ]
Qin, Juan-Juan [1 ,2 ,5 ]
Wan, Jun [1 ,2 ,3 ,4 ]
Wang, Menglong [1 ,2 ,3 ,4 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Cardiol, 238 Jiefang Rd, Wuhan 430060, Peoples R China
[2] Wuhan Univ, Zhongnan Hosp, Dept Geriatr, Wuhan, Peoples R China
[3] Wuhan Univ, Cardiovasc Res Inst, Wuhan, Peoples R China
[4] Hubei Key Lab Cardiol, Wuhan, Peoples R China
[5] Wuhan Univ, Ctr Hlth Aging, Sch Nursing, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
Aortic dissection; apoptotic cell clearance; EDIL3; efferocytosis; inflammation resolution; LC3-associated phagocytosis; DEVELOPMENTAL ENDOTHELIAL LOCUS-1; PHAGOCYTOSIS; DEL-1; OVEREXPRESSION; INHIBITION;
D O I
10.1080/15548627.2024.2367191
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Thoracic aortic dissection (TAD) is a severe disease, characterized by numerous apoptotic vascular smooth muscle cells (VSMCs). EDIL3/Del-1 is a secreted protein involved in macrophage efferocytosis in acute inflammation. Here, we aimed to investigate whether EDIL3 promoted the internalization and degradation of apoptotic VSMCs during TAD. The levels of EDIL3 were decreased in the serum and aortic tissue from TAD mice. Global edil3 knockout (edil3-/-) mice and edil3-/- bone marrow chimeric mice exhibited a considerable exacerbation in beta-aminopropionitrile monofumarate (BAPN)-induced TAD, accompanied with increased apoptotic VSMCs accumulating in the damaged aortic tissue. Two types of phagocytes, RAW264.7 cells and bone marrow-derived macrophages (BMDMs) were used for in vitro efferocytosis assay. edil3-deficient phagocytes exhibited inefficient internalization and degradation of apoptotic VSMCs. Instead, EDIL3 promoted the internalization phase through interacting with phosphatidylserine (PtdSer) on apoptotic VSMCs and binding to the macrophage ITGAV/alpha v-ITGB3/beta 3 integrin. In addition, EDIL3 accelerated the degradation phase through activating LC3-associated phagocytosis (LAP). Mechanically, following the engulfment, EDIL3 enhanced the activity of SMPD1/acid sphingomyelinase in the phagosome through blocking ITGAV-ITGB3 integrin, which facilitates phagosomal reactive oxygen species (ROS) production by NAPDH oxidase CYBB/NOX2. Furthermore, exogenous EDIL3 supplementation alleviated BAPN-induced TAD and promoted apoptotic cell clearance. EDIL3 may be a novel factor for the prevention and treatment of TAD.Abbreviations: BAPN: beta-aminopropionitrile monofumarate; BMDM: bone marrow-derived macrophage; C12FDG: 5-dodecanoylaminofluorescein-di-beta-D-galactopyranoside; CTRL: control; CYBB/NOX2: cytochrome b-245, beta polypeptide; DCFH-DA: 2',7'-dichlorofluorescin diacetate; EDIL3/Del-1: EGF-like repeats and discoidin I-like domains 3; EdU: 5-ethynyl-2'-deoxyuridine; EVG: elastic van Gieson; H&E: hematoxylin and eosin; IL: interleukin; LAP: LC3-associated phagocytosis; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; NAC: N-acetylcysteine; PtdSer: phosphatidylserine; rEDIL3: recombinant EDIL3; ROS: reactive oxygen species; SMPD1: sphingomyelin phosphodiesterase 1; TAD: thoracic aortic dissection; TEM: transmission electron microscopy; VSMC: vascular smooth muscle cell; WT: wild-type
引用
收藏
页码:2405 / 2425
页数:21
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