Distinct Airway Epithelial Stem Cells Hide among Club Cells but Mobilize to Promote Alveolar Regeneration

被引:153
作者
Kathiriya, Jaymin J. [1 ,2 ]
Brumwell, Alexis N. [1 ,2 ]
Jackson, Julia R. [1 ,2 ]
Tang, Xiaodan [1 ,2 ,3 ]
Chapman, Harold A. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Cardiovasc Res Inst, San Francisco, CA 94143 USA
[3] Fudan Univ, Huadong Hosp, Dept Pulm Dis, Shanghai 200040, Peoples R China
关键词
LUNG; REPAIR; DEDIFFERENTIATION; DIFFERENTIATION; PLASTICITY; ORIGIN;
D O I
10.1016/j.stem.2019.12.014
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Lung injury activates specialized adult epithelial progenitors to regenerate the epithelium. Depending on the extent of injury, both remaining alveolar type II cells (AEC2s) and distal airway stem/progenitors mobilize to cover denuded alveoli and restore normal barriers. The major source of airway stem/progenitors other than basal-like cells remains uncertain. Here, we define a distinct subpopulation (similar to 5%) of club-like lineage-negative epithelial progenitors (LNEPs) marked by high H2-K1 expression critical for alveolar repair. Quiescent H2-K1(high) cells account for virtually all in vitro regenerative activity of airway lineages. After bleomycin injury, H2-K1 cells expand and differentiate in vivo to alveolar lineages. However, injured H2-K1 cells eventually develop impaired self-renewal with features of senescence, limiting complete repair. Normal H2-K1(high) cells transplanted into injured lungs differentiate into alveolar cells and rescue lung function. These findings indicate that small subpopulations of specialized stem/progenitors are required for effective lung regeneration and are a potential therapeutic adjunct after major lung injury.
引用
收藏
页码:346 / +
页数:17
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