Rőszer Tamás
Institute for Comparative Molecular Endocrinology, Center of Biomedical Research, University of Ulm, Helmholtzstrasse 8/1, 89081 Ulm, Germany.
Mediators Inflamm. 2015;2015:816460. doi: 10.1155/2015/816460. Epub 2015 May 18.
The alternatively activated or M2 macrophages are immune cells with high phenotypic heterogeneity and are governing functions at the interface of immunity, tissue homeostasis, metabolism, and endocrine signaling. Today the M2 macrophages are identified based on the expression pattern of a set of M2 markers. These markers are transmembrane glycoproteins, scavenger receptors, enzymes, growth factors, hormones, cytokines, and cytokine receptors with diverse and often yet unexplored functions. This review discusses whether these M2 markers can be reliably used to identify M2 macrophages and define their functional subdivisions. Also, it provides an update on the novel signals of the tissue environment and the neuroendocrine system which shape the M2 activation. The possible evolutionary roots of the M2 macrophage functions are also discussed.
交替激活的或M2巨噬细胞是具有高度表型异质性的免疫细胞,在免疫、组织稳态、代谢和内分泌信号传导的界面发挥调控作用。如今,M2巨噬细胞是根据一组M2标志物的表达模式来识别的。这些标志物是跨膜糖蛋白、清道夫受体、酶、生长因子、激素、细胞因子以及具有多样且往往尚未被探索功能的细胞因子受体。本综述讨论了这些M2标志物是否可可靠地用于识别M2巨噬细胞并定义其功能亚群。此外,还提供了关于塑造M2激活的组织环境和神经内分泌系统新信号的最新信息。同时也讨论了M2巨噬细胞功能可能的进化根源。