传出细胞增多
细胞凋亡
细胞生物学
生物
吞噬作用
巨噬细胞
体内
程序性细胞死亡
细胞
体外
遗传学
作者
Michael H. Raymond,Andrew J. Davidson,Yi Shen,D. Tudor,Christopher D. Lucas,Sho Morioka,Justin S. A. Perry,Julia Krapivkina,David Perrais,Linus J. Schumacher,Robert E. Campbell,Will Wood,Kodi S. Ravichandran
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-03-10
卷期号:375 (6585): 1182-1187
被引量:41
标识
DOI:10.1126/science.abl4430
摘要
Apoptosis of cells and their subsequent removal through efferocytosis occurs in nearly all tissues during development, homeostasis, and disease. However, it has been difficult to track cell death and subsequent corpse removal in vivo. We developed a genetically encoded fluorescent reporter, CharON (Caspase and pH Activated Reporter, Fluorescence ON), that could track emerging apoptotic cells and their efferocytic clearance by phagocytes. Using Drosophila expressing CharON, we uncovered multiple qualitative and quantitative features of coordinated clearance of apoptotic corpses during embryonic development. When confronted with high rates of emerging apoptotic corpses, the macrophages displayed heterogeneity in engulfment behaviors, leading to some efferocytic macrophages carrying high corpse burden. Overburdened macrophages were compromised in clearing wound debris. These findings reveal known and unexpected features of apoptosis and macrophage efferocytosis in vivo.
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