EDIL3/Del-1 通过加强凋亡血管平滑肌细胞的内化和降解,预防主动脉夹层。

Autophagy Pub Date : 2024-11-01 Epub Date: 2024-07-01 DOI:10.1080/15548627.2024.2367191
Zheng Yin, Jishou Zhang, Mengmeng Zhao, Jianfang Liu, Yao Xu, Shanshan Peng, Wei Pan, Cheng Wei, Zihui Zheng, Siqi Liu, Juan-Juan Qin, Jun Wan, Menglong Wang
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Global <i>edil3</i> knockout (<i>edil3</i><sup>-/-</sup>) mice and <i>edil3</i><sup>-/-</sup> bone marrow chimeric mice exhibited a considerable exacerbation in β-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. <i>edil3</i>-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/α<sub>v</sub>-ITGB3/β<sub>3</sub> integrin. In addition, EDIL3 accelerated the degradation phase through activating LC3-associated phagocytosis (LAP). 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引用次数: 0

摘要

胸主动脉夹层(TAD)是一种严重疾病,其特征是大量血管平滑肌细胞(VSMC)凋亡。EDIL3/Del-1 是一种分泌蛋白,在急性炎症中参与巨噬细胞的排泄。在此,我们旨在研究 EDIL3 是否能促进 TAD 期间凋亡血管平滑肌细胞的内化和降解。TAD 小鼠血清和主动脉组织中的 EDIL3 水平下降。EDIL3基因敲除(edil3-/-)小鼠和edil3-/-骨髓嵌合小鼠在β-氨基丙腈单富马酸盐(BAPN)诱导的TAD中表现出相当程度的恶化,同时受损的主动脉组织中积累的凋亡VSMC增多。两种类型的吞噬细胞(RAW264.7 细胞和骨髓源性巨噬细胞(BMDMs))被用于体外渗出试验。相反,EDIL3 通过与凋亡 VSMC 上的磷脂酰丝氨酸(PtdSer)相互作用并与巨噬细胞 ITGAV/αv-ITGB3/β3 整合素结合,促进了内化阶段。此外,EDIL3 还通过激活 LC3 相关吞噬(LAP)加速了降解阶段。从机制上讲,吞噬后,EDIL3 通过阻断 ITGAV-ITGB3 整合素增强了吞噬体中 SMPD1/酸性鞘磷脂酶的活性,从而促进了 NAPDH 氧化酶 CYBB/NOX2 产生吞噬体活性氧(ROS)。此外,补充外源 EDIL3 可减轻 BAPN 诱导的 TAD 并促进凋亡细胞的清除。EDIL3 可能是一种预防和治疗 TAD 的新型因子。
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EDIL3/Del-1 prevents aortic dissection through enhancing internalization and degradation of apoptotic vascular smooth muscle cells.

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 β-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/αv-ITGB3/β3 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: β-aminopropionitrile monofumarate; BMDM: bone marrow-derived macrophage; C12FDG: 5-dodecanoylaminofluorescein-di-β-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.

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