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解整合素金属蛋白酶17破坏牛巨噬细胞MER原癌基因酪氨酸激酶的完整性,以阻碍临床乳腺炎中凋亡细胞的清除并促进炎症反应。

A Disintegrin and Metalloproteinase 17 Disrupts Bovine Macrophage MER Proto-Oncogene Tyrosine Kinase Integrity to Impede Apoptotic Cell Clearance and Promote Inflammation in Clinical Mastitis.

作者信息

Wang Jingyi, Li Ming, Zhao Bichen, Chang Renxu, Wu Wenda, Zhang Huijing, Usman Muhammad, Loor Juan J, Xu Chuang

机构信息

Department of Clinical Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Yuanmingyuan West Road, Beijing 100193, China.

School of Food and Biological Engineering, Engineering Research Center of Bio-Process, Ministry of Education, Hefei University of Technology, Hefei 230009, China.

出版信息

J Agric Food Chem. 2025 Jan 8;73(1):549-561. doi: 10.1021/acs.jafc.4c09164. Epub 2024 Dec 28.

Abstract

In clinical mastitis of dairy cows, the abnormal accumulation of apoptotic cells (ACs) and subsequent secondary necrosis and inflammation pose significant concerns, with macrophage-mediated efferocytosis, crucial for ACs clearance, remaining unexplored in this context. In nonruminants, MER proto-oncogene tyrosine kinase (MERTK) receptors are essential for efferocytosis and A Disintegrin and Metalloproteinase 17 (ADAM17) is thought to play a role in regulating MERTK integrity. This study aimed to delineate the in situ role of efferocytosis in clinical mastitis, with a particular focus on the interaction between MERTK and ADAM17 in bovine macrophages. In mastitic mammary tissue, a significant accumulation of ACs was observed, along with active macrophage efferocytosis. Western blotting analysis revealed elevated expressions of MERTK and ADAM17, and immunofluorescence confirmed that MERTK is predominantly localized within CD163 macrophages. Additionally, elevated levels of soluble MERTK (sol-MER) in serum indicated impaired integrity and functionality of MERTK. In vitro experiments with the bovine macrophage cell line Bo-mac cells selectively phagocytosed apoptotic MAC-T cells, a process associated with increased MERTK phosphorylation and an anti-inflammatory phenotype. The activation of ADAM17 by Phorbol 12-myristate 13-acetate (PMA) induced sol-Mer release and impaired efferocytosis, with these effects reversed by the ADAM17 inhibitor TAPI-1. Bo-mac efferocytosis was influenced by the presence and activation of MERTK. Silencing MERTK interrupted efferocytosis, a phenomenon also observed with the inhibition of MERTK phosphorylation by UNC2025, which concurrently suppressed anti-inflammatory cytokine production. These findings suggest that targeting the MERTK-ADAM17 axis could enhance inflammatory resolution, providing a novel therapeutic strategy for dairy cattle health management.

摘要

在奶牛临床乳腺炎中,凋亡细胞(ACs)的异常积累以及随后的继发性坏死和炎症引起了人们的极大关注,而巨噬细胞介导的胞葬作用对于清除ACs至关重要,但在这种情况下尚未得到充分研究。在非反刍动物中,MER原癌基因酪氨酸激酶(MERTK)受体对于胞葬作用至关重要,并且人们认为解整合素和金属蛋白酶17(ADAM17)在调节MERTK完整性方面发挥作用。本研究旨在阐明胞葬作用在临床乳腺炎中的原位作用,特别关注牛巨噬细胞中MERTK和ADAM17之间的相互作用。在乳腺炎乳腺组织中,观察到ACs大量积累,同时巨噬细胞的胞葬作用活跃。蛋白质印迹分析显示MERTK和ADAM17的表达升高,免疫荧光证实MERTK主要定位于CD163巨噬细胞内。此外,血清中可溶性MERTK(sol-MER)水平升高表明MERTK的完整性和功能受损。使用牛巨噬细胞系Bo-mac细胞进行的体外实验表明,其可选择性吞噬凋亡的MAC-T细胞,这一过程与MERTK磷酸化增加和抗炎表型相关。佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)激活ADAM17会诱导sol-Mer释放并损害胞葬作用,而ADAM17抑制剂TAPI-1可逆转这些作用。Bo-mac的胞葬作用受MERTK的存在和激活影响。沉默MERTK会中断胞葬作用,UNC2025抑制MERTK磷酸化时也观察到了这一现象,同时抗炎细胞因子的产生也受到抑制。这些发现表明,针对MERTK-ADAM17轴可能会增强炎症消退,为奶牛健康管理提供一种新的治疗策略。

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