Center for Lung Biology, University of Washington, 815 Mercer Street, Seattle, WA 98109, USA.
Am J Respir Cell Mol Biol. 2012 Oct;47(4):417-26. doi: 10.1165/rcmb.2012-0090OC. Epub 2012 Jun 21.
Macrophages are key orchestrators of the inflammatory and repair responses in the lung, and the diversity of their function is indicated by their polarized states and distinct subpopulations and localization in the lung. Here, we characterized the pulmonary macrophage populations in the interstitial and alveolar compartments during the induction and resolution of acute lung injury induced by Pseudomonas aeruginosa infection. We identified macrophage subpopulations and polarity according to FACS analysis of cell surface protein markers, combined with cell sorting for gene expression using real-time PCR. With these techniques, we validated a novel, alternatively activated (M2) marker (transferrin receptor), and we described three interstitial and alveolar macrophage subpopulations in the lung whose distribution and functional state evolved from the induction to resolution phases of lung injury. Together, these findings indicate the presence and evolution of distinct macrophage subsets in the lung that serve specific niches in regulating the inflammatory response and its resolution. Alterations in the balance and function of these subpopulations could lead to nonresolving acute lung injury.
巨噬细胞是肺部炎症和修复反应的关键协调者,其功能的多样性表现在它们的极化状态、不同的亚群以及在肺部的定位。在这里,我们在铜绿假单胞菌感染诱导的急性肺损伤的诱导和解决过程中,对肺间质和肺泡腔中的巨噬细胞群体进行了特征描述。我们根据细胞表面蛋白标记物的 FACS 分析,结合实时 PCR 的细胞分选,对巨噬细胞亚群和极性进行了鉴定。通过这些技术,我们验证了一个新的、替代激活(M2)标记物(转铁蛋白受体),并描述了肺内三种间质和肺泡巨噬细胞亚群,它们在肺损伤的诱导到解决阶段的分布和功能状态发生了演变。总的来说,这些发现表明,在调节炎症反应及其解决过程中,肺部存在并进化出了不同的巨噬细胞亚群。这些亚群的平衡和功能的改变可能导致非解决性急性肺损伤。