Expression and characterization of v5 integrin on intestinal macrophages

被引:21
|
作者
Kumawat, Ashok K. [1 ,2 ]
Yu, Chen [3 ]
Mann, Elizabeth A. [1 ]
Schridde, Anika [1 ]
Finnemann, Silvia C. [3 ]
Mowat, Allan McI [1 ]
机构
[1] Univ Glasgow, Ctr Immunobiol, Inst Infect Immun & Inflammat, Sir Graeme Davies Bldg,120 Univ Pl, Glasgow G12 8TA, Lanark, Scotland
[2] Orebro Univ, Sch Med Sci, Orebro, Sweden
[3] Fordham Univ, Dept Biol Sci, Ctr Canc Genet Dis & Gene Regulat, Bronx, NY 10458 USA
基金
美国国家卫生研究院;
关键词
Homeostasis; Intestine; Macrophage; Phagocytosis; v5; integrin; ALPHA-V-BETA-5; INTEGRIN; RETINAL PHAGOCYTOSIS; ACTIVATION; MICE; BINDING; MFG-E8; CELLS;
D O I
10.1002/eji.201747318
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages play a crucial role in maintaining homeostasis in the intestine, but the underlying mechanisms have not yet been elucidated fully. Here, we show for the first time that mature intestinal macrophages in mouse intestine express high levels of v5 integrin, which acts as a receptor for the uptake of apoptotic cells and can activate molecules involved in several aspects of tissue homeostasis such as angiogenesis and remodeling of the ECM. v5 is not expressed by other immune cells in the intestine, is already present on intestinal macrophages soon after birth, and its expression is not dependent on the microbiota. In adults, v5 is induced during the differentiation of monocytes in response to the local environment and it confers intestinal macrophages with the ability to promote engulfment of apoptotic cells via engagement of the bridging molecule milk fat globule EGF-like molecule 8. In the absence of v5, there are fewer monocytes in the mucosa and mature intestinal macrophages have decreased expression of metalloproteases and IL 10. Mice lacking v5 on haematopoietic cells show increased susceptibility to chemical colitis and we conclude that v5 contributes to the tissue repair by regulating the homeostatic properties of intestinal macrophages.
引用
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页码:1181 / 1187
页数:7
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