Dos Anjos Cassado Alexandra
Immunology Department, São Paulo University, São Paulo, SP, Brazil.
UniSALESIANO, Auxilium Salesian Catholic University Center, Araçatuba, SP, Brazil.
Results Probl Cell Differ. 2017;62:161-179. doi: 10.1007/978-3-319-54090-0_7.
Tissue macrophages are a heterogeneous cell population residing in all body tissues that contribute to the maintenance of homeostasis and trigger immune activation in response to injurious stimuli. This heterogeneity may be associated with tissue-specific functions; however, the presence of distinct macrophage populations within the same microenvironment indicates that macrophage heterogeneity may also be influenced outside of tissue specialization. The F4/80 molecule was established as a unique marker of murine macrophages when a monoclonal antibody was found to recognize an antigen exclusively expressed by these cells. However, recent research has shown that F4/80 is expressed by other immune cells and is not equivalently expressed across tissue-specific macrophage lineages, including those residing in the same microenvironment, such as the peritoneum and spleen. In this context, two murine macrophage subtypes with distinct F4/80 expression patterns were recently found to coexist in the peritoneum, termed large peritoneal macrophages (LPMs) and small peritoneal macrophages (SPMs). However, the presence of phenotypic and functional heterogeneous macrophage subpopulations in the spleen was already known. Thus, although F4/80 surface expression continues to be the best method to identify tissue macrophages, additional molecules must also be examined to distinguish these cells from other immune cells.
组织巨噬细胞是存在于所有身体组织中的异质性细胞群体,有助于维持体内稳态,并在受到损伤性刺激时触发免疫激活。这种异质性可能与组织特异性功能相关;然而,同一微环境中存在不同的巨噬细胞群体表明,巨噬细胞的异质性也可能受到组织特化之外的因素影响。当发现一种单克隆抗体能识别仅由这些细胞表达的抗原时,F4/80分子被确立为小鼠巨噬细胞的独特标志物。然而,最近的研究表明,F4/80也由其他免疫细胞表达,并且在不同组织特异性巨噬细胞谱系中表达并不相同,包括那些存在于同一微环境中的巨噬细胞,如腹膜和脾脏中的巨噬细胞。在此背景下,最近发现腹膜中存在两种具有不同F4/80表达模式的小鼠巨噬细胞亚型,分别称为大腹膜巨噬细胞(LPMs)和小腹膜巨噬细胞(SPMs)。然而,脾脏中存在表型和功能异质性的巨噬细胞亚群这一情况早已为人所知。因此,尽管F4/80表面表达仍然是识别组织巨噬细胞的最佳方法,但还必须检测其他分子,以将这些细胞与其他免疫细胞区分开来。