Gonzalez-Mejia M Elba, Doseff Andrea I
Department of Internal Medicine, Division of Pulmonary and Critical Care, The Ohio State University Columbus, OH, USA.
Front Biosci (Landmark Ed). 2009 Jan 1;14(7):2413-31. doi: 10.2741/3387.
Monocytes and macrophages are central cells of the innate immune system, responding to a diverse repertoire of pathogens. These cells originate from a common myeloid precursor in the bone marrow and while sharing responsibilities during innate immunity, differ greatly in their lifespan. Normally, blood monocytes live for just few days before undergoing apoptosis. Macrophages, in contrast, live up for months. Monocytes' lifespan can switch dramatically, from prolonged survival during inflammation to apoptosis as inflammation resolves. Interestingly, many of the mechanisms mediating survival during inflammation and cancer also operate in monocyte/macrophage differentiation. Differentiation and inflammatory stimuli determine monocyte/macrophage lifespan, by blocking the apoptotic pathway and activating a myriad of survival pathways. How these complicated networks of survival and apoptotic regulators are integrated remains yet to be fully elucidated. The present review summarizes the different monocytes' subpopulations and their function during pathogen recognition. We discuss the role of the caspases and the mechanisms that determine monocytes/macrophages fate highlighting their significance in the regulation of inflammatory diseases.
单核细胞和巨噬细胞是先天性免疫系统的核心细胞,可对多种病原体作出反应。这些细胞起源于骨髓中的共同髓样前体,虽然在先天性免疫过程中分担责任,但其寿命却有很大差异。正常情况下,血液中的单核细胞在经历凋亡前仅存活几天。相比之下,巨噬细胞可存活数月。单核细胞的寿命可发生显著变化,从炎症期间的延长存活到炎症消退时的凋亡。有趣的是,许多介导炎症和癌症期间存活的机制也在单核细胞/巨噬细胞分化过程中发挥作用。分化和炎症刺激通过阻断凋亡途径并激活众多存活途径来决定单核细胞/巨噬细胞的寿命。这些复杂的存活和凋亡调节因子网络如何整合仍有待充分阐明。本综述总结了不同的单核细胞亚群及其在病原体识别过程中的功能。我们讨论了半胱天冬酶的作用以及决定单核细胞/巨噬细胞命运的机制,强调了它们在炎症性疾病调节中的重要性。