相(物质)
分子生物学
生物
免疫学
物理
医学
量子力学
作者
Naoki Ikeda,Kenichi Asano,Kenta Kikuchi,Yuka Uchida,Hiroki Ikegami,Ryo Takagi,Satoshi Yotsumoto,Tomoki Shibuya,Chieko Makino‐Okamura,Hidehiro Fukuyama,Takashi Watanabe,Masaki Ohmuraya,Kimi Araki,Gen Nishitai,Masato Tanaka
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2018-10-05
卷期号:3 (28)
被引量:76
标识
DOI:10.1126/sciimmunol.aat0207
摘要
Ly6Chi monocytes migrate to injured sites and induce inflammation in the acute phase of tissue injury. However, once the causes of tissue injury are eliminated, monocyte-derived macrophages contribute to the resolution of inflammation and tissue repair. It remains unclear whether the emergence of these immunoregulatory macrophages is attributed to the phenotypic conversion of inflammatory monocytes in situ or to the recruitment of bone marrow-derived regulatory cells de novo. Here, we identified a subpopulation of Ly6Chi monocytes that contribute to the resolution of inflammation and tissue repair. Ym1+Ly6Chi monocytes greatly expanded in bone marrow during the recovery phase of systemic inflammation or tissue injury. Ym1+Ly6Chi monocytes infiltrating into an injured site exhibited immunoregulatory and tissue-reparative phenotypes. Deletion of Ym1+Ly6Chi monocytes resulted in delayed recovery from colitis. These results demonstrate that a distinct monocyte subpopulation destined to act in immunoregulation is generated in bone marrow and participates in resolution of inflammation and tissue repair.
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