Singapore Immunology Network (SIgN), A(∗)STAR, 8A Biomedical Grove, Immunos Building, Level 3, Singapore 138648, Singapore; Shanghai Institute of Immunology, Shanghai JiaoTong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.
Unit of Immunoregulation and Mucosal Immunology, VIB Inflammation Research Center, Ghent 9052, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent 9000, Belgium.
Immunity. 2016 Mar 15;44(3):439-449. doi: 10.1016/j.immuni.2016.02.024.
Defining the origins and developmental pathways of tissue-resident macrophages should help refine our understanding of the role of these cells in various disease settings and enable the design of novel macrophage-targeted therapies. In recent years the long-held belief that macrophage populations in the adult are continuously replenished by monocytes from the bone marrow (BM) has been overturned with the advent of new techniques to dissect cellular ontogeny. The new paradigm suggests that several tissue-resident macrophage populations are seeded during waves of embryonic hematopoiesis and self-maintain independently of BM contribution during adulthood. However, the exact nature of the embryonic progenitors that give rise to adult tissue-resident macrophages is still debated, and the mechanisms enabling macrophage population maintenance in the adult are undefined. Here, we review the emergence of these concepts and discuss current controversies and future directions in macrophage biology.
定义组织驻留巨噬细胞的起源和发育途径应该有助于我们更深入地了解这些细胞在各种疾病状态下的作用,并能够设计针对巨噬细胞的新型治疗方法。近年来,随着剖析细胞发生的新技术的出现,人们颠覆了长期以来认为成年巨噬细胞群体不断由骨髓中的单核细胞补充的观点。新的范例表明,在胚胎造血的几个波次中,几种组织驻留巨噬细胞群体被播种,并且在成年期独立于骨髓贡献而自我维持。然而,产生成年组织驻留巨噬细胞的胚胎前体的确切性质仍存在争议,并且在成年期维持巨噬细胞群体的机制尚不清楚。在这里,我们回顾了这些概念的出现,并讨论了巨噬细胞生物学中当前的争议和未来的方向。