Mechanisms of Organ Injury and Repair by Macrophages

被引:481
作者
Vannella, Kevin M. [1 ]
Wynn, Thomas A. [1 ]
机构
[1] NIAID, Immunopathogenesis Sect, Parasit Dis Lab, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 79 | 2017年 / 79卷
基金
美国国家卫生研究院;
关键词
fibrosis; pulmonary; hepatic; cardiovascular; gut; brain; TISSUE-RESIDENT MACROPHAGES; ERYTHRO-MYELOID PROGENITOR; LIVER FIBROSIS; SKELETAL-MUSCLE; GROWTH-FACTOR; SPINAL-CORD; PHARMACOLOGICAL INHIBITION; CHEMOATTRACTANT PROTEIN-1; INTERLEUKIN-10; PRODUCTION; ALVEOLAR MACROPHAGES;
D O I
10.1146/annurev-physiol-022516-034356
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Macrophages regulate tissue regeneration following injury. They can worsen tissue injury by producing reactive oxygen species and other toxic mediators that disrupt cell metabolism, induce apoptosis, and exacerbate ischemic injury. However, they also produce a variety of growth factors, such as IGF-1, VEGF-alpha, TGF-beta, and Wnt proteins that regulate epithelial and endothelial cell proliferation, myofibroblast activation, stem and tissue progenitor cell differentiation, and angiogenesis. Proresolving macrophages in turn restore tissue homeostasis by functioning as anti-inflammatory cells, and macrophage-derived matrix metalloproteinases regulate fibrin and collagen turnover. However, dysregulated macrophage function impairs wound healing and contributes to the development of fibrosis. Consequently, the mechanisms that regulate these different macrophage activation states have become active areas of research. In this review, we discuss the common and unique mechanisms by which macrophages instruct tissue repair in the liver, nervous system, heart, lung, skeletal muscle, and intestine and illustrate how macrophages might be exploited therapeutically.
引用
收藏
页码:593 / 617
页数:25
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