生物
干细胞
细胞生物学
再生(生物学)
肺
电池类型
谱系(遗传)
重组酶
细胞
免疫学
遗传学
基因
内科学
医学
重组
作者
Kuo Liu,Xinfeng Meng,Zixin Liu,Muxue Tang,Zan Lv,Xiuzhen Huang,Hengwei Jin,Ximeng Han,Xiuxiu Liu,Wenjuan Pu,Huan Zhu,Bin Zhou
出处
期刊:Cell
[Elsevier]
日期:2024-04-04
卷期号:187 (10): 2428-2445.e20
被引量:9
标识
DOI:10.1016/j.cell.2024.03.010
摘要
Alveolar type 2 (AT2) cells are stem cells of the alveolar epithelia. Previous genetic lineage tracing studies reported multiple cellular origins for AT2 cells after injury. However, conventional lineage tracing based on Cre-loxP has the limitation of non-specific labeling. Here, we introduced a dual recombinase-mediated intersectional genetic lineage tracing approach, enabling precise investigation of AT2 cellular origins during lung homeostasis, injury, and repair. We found AT1 cells, being terminally differentiated, did not contribute to AT2 cells after lung injury and repair. Distinctive yet simultaneous labeling of club cells, bronchioalveolar stem cells (BASCs), and existing AT2 cells revealed the exact contribution of each to AT2 cells post-injury. Mechanistically, Notch signaling inhibition promotes BASCs but impairs club cells' ability to generate AT2 cells during lung repair. This intersectional genetic lineage tracing strategy with enhanced precision allowed us to elucidate the physiological role of various epithelial cell types in alveolar regeneration following injury.
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