Rutherford M S, Witsell A, Schook L B
Department of Animal Sciences, University of Illinois, Urbana 61801.
J Leukoc Biol. 1993 May;53(5):602-18. doi: 10.1002/jlb.53.5.602.
Macrophage populations exhibit a wide range of antigenic and functional phenotypes, including cytokine production, response to immunomodulatory stimuli, and clearance of pathogens. The expanding clinical exploitation of recombinant growth factors and cytokines with the potential to regulate the production and function of peripheral macrophage populations necessitates an increased understanding of the mechanisms by which functionally distinct macrophage populations arise as well as the ramifications of macrophage heterogeneity. The present review summarizes recent data which supports multiple mechanisms by which heterogeneous macrophage populations arise: 1) differential signals experienced within diverse tissue microenvironments; 2) developmentally-staged expression of specific functions; 3) clonal variation of myeloid progenitor cells; and 4) alternate hematopoietic stimulation. These data show that the above processes are not mutually exclusive and that each likely contributes to the observed heterogeneity of peripheral macrophage populations.
巨噬细胞群体表现出广泛的抗原和功能表型,包括细胞因子产生、对免疫调节刺激的反应以及病原体清除。重组生长因子和细胞因子在临床上的应用不断扩大,它们有可能调节外周巨噬细胞群体的产生和功能,这就需要我们更多地了解功能不同的巨噬细胞群体产生的机制以及巨噬细胞异质性的影响。本综述总结了最近的数据,这些数据支持了异质性巨噬细胞群体产生的多种机制:1)在不同组织微环境中经历的差异信号;2)特定功能的发育阶段表达;3)髓系祖细胞的克隆变异;4)交替造血刺激。这些数据表明,上述过程并非相互排斥,每一个过程都可能导致观察到的外周巨噬细胞群体的异质性。