| Literature DB >> 31978363 |
Jaymin J Kathiriya1, Alexis N Brumwell1, Julia R Jackson1, Xiaodan Tang2, Harold A Chapman3.
Abstract
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 (∼5%) of club-like lineage-negative epithelial progenitors (LNEPs) marked by high H2-K1 expression critical for alveolar repair. Quiescent H2-K1high 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-K1high 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.Entities:
Keywords: MHC(high) airway progenitors; alveolar injury and regeneration; bleomycin injury; dedifferentiation; lung epithelial stem cells; oxygenation; single cell transcriptomics; transplantation
Mesh:
Year: 2020 PMID: 31978363 PMCID: PMC7233183 DOI: 10.1016/j.stem.2019.12.014
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633