Immunopharmacology, Department of Biochemistry and Immunology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Department of Microbiology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Int J Biochem Cell Biol. 2021 Dec;141:106095. doi: 10.1016/j.biocel.2021.106095. Epub 2021 Oct 13.
Macrophages are a heterogeneous population of myeloid cells with phenotype and function modulated according to the microenvironment in which they are found. The lung resident macrophages known as Alveolar Macrophages (AM) and Interstitial Macrophages (IM) are localized in two different compartments. During lung homeostasis, macrophages can remove inhaled particulates, cellular debris and contribute to some metabolic processes. Macrophages may assume a pro-inflammatory phenotype after being classically activated (M1) or anti-inflammatory when being alternatively activated (M2). M1 and M2 have different transcription profiles and act by eliminating bacteria, viruses and fungi from the host or repairing the damage triggered by inflammation, respectively. Nevertheless, macrophages also may contribute to lung damage during persistent inflammation or continuous exposure to antigens. In this review, we discuss the origin and function of pulmonary macrophages in the context of homeostasis, infectious and non-infectious lung diseases.
巨噬细胞是一类异质性的髓系细胞,其表型和功能根据其所处的微环境而发生变化。肺内固有巨噬细胞(肺泡巨噬细胞和间质巨噬细胞)定位于两个不同的部位。在肺稳态时,巨噬细胞可以清除吸入的颗粒、细胞碎片,并参与某些代谢过程。巨噬细胞在经典激活后可呈现促炎表型(M1),或在替代激活时呈现抗炎表型(M2)。M1 和 M2 具有不同的转录谱,分别通过消除宿主中的细菌、病毒和真菌,或修复炎症引发的损伤来发挥作用。然而,巨噬细胞在持续炎症或持续暴露于抗原时也可能导致肺损伤。在本篇综述中,我们讨论了肺巨噬细胞在稳态、感染性和非感染性肺疾病背景下的起源和功能。
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