Naito M
Second Department of Pathology, Niigata University School of Medicine, Japan.
Arch Histol Cytol. 1993 Oct;56(4):331-51. doi: 10.1679/aohc.56.331.
Macrophages, which are heterogeneous populations existing in various tissues and organs, are responsible for numerous metabolic, immunological, and inflammatory processes in physiological and pathological conditions. Macrophage heterogeneity is observed from early ontogeny. Primitive macrophages first develop in yolk sac hematopoiesis, by-passing the differentiation pathway of the monocytic series to differentiate into fetal macrophages in various tissues. Monocytic cells are a minor cell population in the early fetal period, and increase in the late stage. Primitive/fetal macrophages proliferate and survive in loco in the fetal period and reside as resident macrophages after birth. In adult animals, monocytes are differentiated from promonocytes derived from pluripotent stem cells in bone marrow. Monocytes exude in inflammatory foci and differentiate into exudate macrophages, exudate-resident macrophages and peroxidase-negative macrophages, but not resident macrophages. Monocyte-derived macrophages are a short-lived and non-proliferating cell population. Tissue (resident) macrophages proliferate and maintain their population by self renewal. In mice rendered monocytopenic by administration of a bone-seeking isotope, strontium-89, tissue resident macrophages maintained their population for 6 weeks. Resident macrophages in the liver formed glucan-induced granulomas in this monocytopenic model. In macrophage colony stimulating factor (M-CSF)-deficient mice (op/op), monocytes as well as tissue macrophages are deficient. However, M-CSF-independent tissue macrophages and Langerhans/dendritic cells are present in the defective condition of monocyte differentiation into macrophages, indicating that differentiation pathways of tissue macrophages and nonlymphoid dendritic cells are different from those of monocytes. In cultures supplemented with various colony stimulating factors (CSFs), heterogenous macrophage populations were generated. These in vivo and in vitro findings suggest that the phenotypic and functional heterogeneity of macrophages reflects complex macrophage differentiation mechanisms and that CSFs are important factors in the formation of a microenvironment for macrophage differentiation.
巨噬细胞是存在于各种组织和器官中的异质性群体,在生理和病理条件下负责众多的代谢、免疫和炎症过程。巨噬细胞的异质性在个体发育早期就已被观察到。原始巨噬细胞首先在卵黄囊造血过程中发育,绕过单核细胞系的分化途径,在各种组织中分化为胎儿巨噬细胞。单核细胞在胎儿早期是次要的细胞群体,在后期增加。原始/胎儿巨噬细胞在胎儿期在局部增殖并存活,出生后作为驻留巨噬细胞存在。在成年动物中,单核细胞由骨髓中多能干细胞衍生的前单核细胞分化而来。单核细胞渗出到炎症灶中,分化为渗出性巨噬细胞、渗出性驻留巨噬细胞和过氧化物酶阴性巨噬细胞,但不会分化为驻留巨噬细胞。单核细胞衍生的巨噬细胞是寿命短且不增殖的细胞群体。组织(驻留)巨噬细胞通过自我更新进行增殖并维持其群体数量。在用骨靶向同位素锶 - 89使小鼠单核细胞减少的情况下,组织驻留巨噬细胞维持其群体数量达6周。在这个单核细胞减少模型中,肝脏中的驻留巨噬细胞形成了葡聚糖诱导的肉芽肿。在巨噬细胞集落刺激因子(M - CSF)缺陷的小鼠(op/op)中,单核细胞以及组织巨噬细胞都有缺陷。然而,在单核细胞分化为巨噬细胞存在缺陷的情况下,存在不依赖M - CSF的组织巨噬细胞和朗格汉斯/树突状细胞,这表明组织巨噬细胞和非淋巴样树突状细胞的分化途径与单核细胞不同。在补充了各种集落刺激因子(CSF)的培养物中,产生了异质性的巨噬细胞群体。这些体内和体外的研究结果表明,巨噬细胞的表型和功能异质性反映了复杂的巨噬细胞分化机制,并且CSF是形成巨噬细胞分化微环境的重要因素。