Author
Listed:
- Brian Lin
(Massachusetts General Hospital
Harvard Stem Cell Institute
Broad Institute
Tufts University)
- Viral S. Shah
(Massachusetts General Hospital
Harvard Stem Cell Institute
Broad Institute
Harvard Medical School)
- Chaim Chernoff
(Massachusetts General Hospital
Harvard Stem Cell Institute
Harvard)
- Jiawei Sun
(Massachusetts General Hospital
Harvard Stem Cell Institute)
- Gergana G. Shipkovenska
(Massachusetts General Hospital
Harvard Stem Cell Institute
Broad Institute)
- Vladimir Vinarsky
(Massachusetts General Hospital
Harvard Stem Cell Institute
Harvard Medical School)
- Avinash Waghray
(Massachusetts General Hospital
Harvard Stem Cell Institute
Broad Institute)
- Jiajie Xu
(Massachusetts General Hospital
Harvard Stem Cell Institute)
- Andrew D. Leduc
(Northeastern University)
- Constantin A. Hintschich
(Tufts University
Regensburg University Hospital
Massachusetts Eye and Ear Infirmary)
- Manalee Vishnu Surve
(Massachusetts General Hospital
Harvard Stem Cell Institute
Broad Institute)
- Yanxin Xu
(Massachusetts General Hospital
Harvard Stem Cell Institute)
- Diane E. Capen
(Massachusetts General Hospital)
- Jorge Villoria
(Massachusetts General Hospital
Harvard Stem Cell Institute)
- Zhixun Dou
(Massachusetts General Hospital
Harvard Stem Cell Institute)
- Lida P. Hariri
(Harvard Medical School
Harvard Medical School)
- Jayaraj Rajagopal
(Massachusetts General Hospital
Harvard Stem Cell Institute
Broad Institute
Harvard Medical School)
Abstract
Airway hillocks are stratified epithelial structures of unknown function1. Hillocks persist for months and have a unique population of basal stem cells that express genes associated with barrier function and cell adhesion. Hillock basal stem cells continually replenish overlying squamous barrier cells. They exhibit dramatically higher turnover than the abundant, largely quiescent classic pseudostratified airway epithelium. Hillocks resist a remarkably broad spectrum of injuries, including toxins, infection, acid and physical injury because hillock squamous cells shield underlying hillock basal stem cells from injury. Hillock basal stem cells are capable of massive clonal expansion that is sufficient to resurface denuded airway, and eventually regenerate normal airway epithelium with each of its six component cell types. Hillock basal stem cells preferentially stratify and keratinize in the setting of retinoic acid signalling inhibition, a known cause of squamous metaplasia2,3. Here we show that mouse hillock expansion is the cause of vitamin A deficiency-induced squamous metaplasia. Finally, we identify human hillocks whose basal stem cells generate functional squamous barrier structures in culture. The existence of hillocks reframes our understanding of airway epithelial regeneration. Furthermore, we show that hillocks are one origin of ‘squamous metaplasia’, which is long thought to be a precursor of lung cancer.
Suggested Citation
Brian Lin & Viral S. Shah & Chaim Chernoff & Jiawei Sun & Gergana G. Shipkovenska & Vladimir Vinarsky & Avinash Waghray & Jiajie Xu & Andrew D. Leduc & Constantin A. Hintschich & Manalee Vishnu Surve , 2024.
"Airway hillocks are injury-resistant reservoirs of unique plastic stem cells,"
Nature, Nature, vol. 629(8013), pages 869-877, May.
Handle:
RePEc:nat:nature:v:629:y:2024:i:8013:d:10.1038_s41586-024-07377-1
DOI: 10.1038/s41586-024-07377-1
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