Mege Jean-Louis, Capo Christian
Unité de recherche sur les maladies infectieuses transmissibles et émergentes, CNRS-IRD UMR 6236, Université de la Méditerranée, 27, boulevard Jean Moulin, 13385 Marseille Cedex 5, France.
Med Sci (Paris). 2010 Jan;26(1):83-8. doi: 10.1051/medsci/201026183.
Converging studies show that M1 and M2 macrophages are functionally polarized in response to host mediators. Gene expression profiling of macrophages reveals that various bacteria induce the transcriptional activity of a common host response that includes genes belonging to the M1 program. The microbicidal machinery of M1 macrophages allows them to participate to the clearing of acute infections. However, excessive or prolonged M1 polarization can lead to tissue injury and contribute to pathogenesis. The so-called M2 macrophages play a critical role in the resolution of inflammation by producing anti-inflammatory mediators. These M2 macrophages cover a continuum of cells with different phenotypic and functional properties. Different bacterial pathogens escape from clearing by manipulating functions of M1 macrophages. It has recently been demonstrated that specific M2 programs induced in macrophages by bacterial pathogens are associated with the chronic evolution of infectious diseases.
多项研究表明,M1和M2巨噬细胞会响应宿主介质而发生功能极化。巨噬细胞的基因表达谱分析显示,多种细菌可诱导一种常见宿主反应的转录活性,该反应包括属于M1程序的基因。M1巨噬细胞的杀菌机制使其能够参与清除急性感染。然而,过度或长期的M1极化会导致组织损伤并促进发病机制。所谓的M2巨噬细胞通过产生抗炎介质在炎症消退中起关键作用。这些M2巨噬细胞涵盖了具有不同表型和功能特性的一系列细胞。不同的细菌病原体通过操纵M1巨噬细胞的功能逃避清除。最近已证明,细菌病原体在巨噬细胞中诱导的特定M2程序与传染病的慢性演变有关。