| Literature DB >> 30291130 |
Naoki Ikeda1, Kenichi Asano1, Kenta Kikuchi1, Yoshimi Uchida1, Hiroki Ikegami1, Ryo Takagi1, Satoshi Yotsumoto1, Takumi Shibuya1, Chieko Makino-Okamura2, Hidehiro Fukuyama2, Takashi Watanabe3, Masaki Ohmuraya4, Kimi Araki5, Gen Nishitai1, Masato Tanaka6.
Abstract
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.Entities:
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Year: 2018 PMID: 30291130 DOI: 10.1126/sciimmunol.aat0207
Source DB: PubMed Journal: Sci Immunol ISSN: 2470-9468