生物
巨噬细胞
间皮
细胞生物学
腹膜腔
炎症
表型
CD44细胞
病理
免疫学
腹膜
细胞
解剖
体外
基因
遗传学
医学
出处
期刊:Cell
[Cell Press]
日期:2016-04-01
卷期号:165 (3): 668-678
被引量:406
标识
DOI:10.1016/j.cell.2016.03.009
摘要
A key feature of inflammation is the timely recruitment of leukocytes, including monocytes, from blood into tissues, the latter maturing into macrophages over a period of 2-3 days. Using multi-channel spinning disk microscopy, we identified a rapid pathway of macrophage recruitment into an injured organ via a non-vascular route requiring no maturation from monocytes. In response to a sterile injury in liver, a reservoir of fully mature F4/80(hi)GATA6(+) peritoneal cavity macrophages rapidly invaded into afflicted tissue via direct recruitment across the mesothelium. The invasion was dependent on CD44 and DAMP molecule ATP and resulted in rapid replication and switching of macrophage toward an alternatively activated phenotype. These macrophages dismantled the nuclei of necrotic cells releasing DNA and forming a cover across the injury site. Rapid invasion of mature macrophages from body cavity with capacity for induction of reparative phenotype may impact altered tissues ranging from trauma to infections to cancer. VIDEO ABSTRACT.
科研通智能强力驱动
Strongly Powered by AbleSci AI