Immunopathogenesis Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892; email:
Annu Rev Physiol. 2017 Feb 10;79:593-617. doi: 10.1146/annurev-physiol-022516-034356. Epub 2016 Dec 7.
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-α, TGF-β, 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.
巨噬细胞调节损伤后的组织再生。它们通过产生活性氧物种和其他有毒介质来加重组织损伤,这些物质会破坏细胞代谢、诱导细胞凋亡,并加重缺血性损伤。然而,它们也产生多种生长因子,如 IGF-1、VEGF-α、TGF-β 和 Wnt 蛋白,这些生长因子调节上皮细胞和内皮细胞的增殖、肌成纤维细胞的激活、干细胞和组织祖细胞的分化以及血管生成。相反,促修复巨噬细胞通过发挥抗炎细胞的作用来恢复组织内稳态,并且巨噬细胞衍生的基质金属蛋白酶调节纤维蛋白和胶原的转化。然而,巨噬细胞功能失调会损害伤口愈合,并导致纤维化的发展。因此,调节这些不同的巨噬细胞激活状态的机制已成为研究的活跃领域。在这篇综述中,我们讨论了巨噬细胞在肝脏、神经系统、心脏、肺、骨骼肌和肠道中指导组织修复的常见和独特机制,并说明了如何从治疗的角度利用巨噬细胞。