炎症
膜联蛋白A1
巨噬细胞
重编程
纤溶酶
膜联蛋白
细胞生物学
免疫学
化学
生物
细胞
流式细胞术
生物化学
酶
体外
作者
Michelle A. Sugimoto,Ana Luíza C. Ribeiro,Bruno Rocha Cordeiro Costa,Juliana P. Vago,Kátia Maciel Lima,Fernanda S. Carneiro,Mylena Maira Oliveira Ortiz,Graziele L. Negreiros-Lima,Aline A. F. Carmo,Renata Maria Rocha,Denise Perez,Alessandra C. Reis,Vanessa Pinho,Lindsey A. Miles,Cristiana Couto Garcia,Mauro Martins Teixeira,Lirlandia Pires Sousa
出处
期刊:Blood
[Elsevier BV]
日期:2017-03-20
卷期号:129 (21): 2896-2907
被引量:140
标识
DOI:10.1182/blood-2016-09-742825
摘要
]). Pleural injection of Plg/Pla also increased M2 markers (CD206 and arginase-1) and secretory products (transforming growth factor β and interleukin-6) and decreased the expression of inducible nitric oxide synthase (M1 marker). During the resolving phase of lipopolysaccharide (LPS)-induced inflammation when resolving macrophages predominate, we found increased Plg expression and Pla activity, further supporting a link between the Plg/Pla system and key cellular events in resolution. Indeed, Plg or Pla given at the peak of inflammation promoted resolution by decreasing neutrophil numbers and increasing neutrophil apoptosis and efferocytosis in a serine-protease inhibitor-sensitive manner. Next, we confirmed the ability of Plg/Pla to both promote efferocytosis and override the prosurvival effect of LPS via annexin A1. These findings suggest that Plg and Pla regulate several key steps in inflammation resolution, namely, neutrophil apoptosis, macrophage reprogramming, and efferocytosis, which have a major impact on the establishment of an efficient resolution process.
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