Author
Listed:
- Sekyu Choi
(Harvard University
Harvard Stem Cell Institute)
- Bing Zhang
(Harvard University
Harvard Stem Cell Institute
School of Life Science, Westlake University)
- Sai Ma
(Harvard University
Department of Biology and Koch Institute, MIT
Broad Institute of Harvard and MIT)
- Meryem Gonzalez-Celeiro
(Harvard University
Harvard Stem Cell Institute)
- Daniel Stein
(Harvard University
Harvard Stem Cell Institute)
- Xin Jin
(Harvard University
Harvard Stem Cell Institute
Broad Institute of Harvard and MIT)
- Seung Tea Kim
(Harvard University
Harvard Stem Cell Institute)
- Yuan-Lin Kang
(Harvard University
Harvard Stem Cell Institute)
- Antoine Besnard
(Harvard Stem Cell Institute
Massachusetts General Hospital
Massachusetts General Hospital, Harvard Medical School
CNRS, Institut de Génomique Fonctionnelle)
- Amelie Rezza
(Icahn School of Medicine at Mount Sinai
Icahn School of Medicine at Mount Sinai
genOway)
- Laura Grisanti
(Icahn School of Medicine at Mount Sinai
Icahn School of Medicine at Mount Sinai)
- Jason D. Buenrostro
(Harvard University
Harvard Stem Cell Institute
Broad Institute of Harvard and MIT)
- Michael Rendl
(Icahn School of Medicine at Mount Sinai
Icahn School of Medicine at Mount Sinai
Icahn School of Medicine at Mount Sinai)
- Matthias Nahrendorf
(Massachusetts General Hospital Research Institute, Harvard Medical School
Massachusetts General Hospital, Harvard Medical School
University Hospital Würzburg)
- Amar Sahay
(Harvard Stem Cell Institute
Broad Institute of Harvard and MIT
Massachusetts General Hospital
Massachusetts General Hospital, Harvard Medical School)
- Ya-Chieh Hsu
(Harvard University
Harvard Stem Cell Institute)
Abstract
Chronic, sustained exposure to stressors can profoundly affect tissue homeostasis, although the mechanisms by which these changes occur are largely unknown. Here we report that the stress hormone corticosterone—which is derived from the adrenal gland and is the rodent equivalent of cortisol in humans—regulates hair follicle stem cell (HFSC) quiescence and hair growth in mice. In the absence of systemic corticosterone, HFSCs enter substantially more rounds of the regeneration cycle throughout life. Conversely, under chronic stress, increased levels of corticosterone prolong HFSC quiescence and maintain hair follicles in an extended resting phase. Mechanistically, corticosterone acts on the dermal papillae to suppress the expression of Gas6, a gene that encodes the secreted factor growth arrest specific 6. Restoring Gas6 expression overcomes the stress-induced inhibition of HFSC activation and hair growth. Our work identifies corticosterone as a systemic inhibitor of HFSC activity through its effect on the niche, and demonstrates that the removal of such inhibition drives HFSCs into frequent regeneration cycles, with no observable defects in the long-term.
Suggested Citation
Sekyu Choi & Bing Zhang & Sai Ma & Meryem Gonzalez-Celeiro & Daniel Stein & Xin Jin & Seung Tea Kim & Yuan-Lin Kang & Antoine Besnard & Amelie Rezza & Laura Grisanti & Jason D. Buenrostro & Michael Re, 2021.
"Corticosterone inhibits GAS6 to govern hair follicle stem-cell quiescence,"
Nature, Nature, vol. 592(7854), pages 428-432, April.
Handle:
RePEc:nat:nature:v:592:y:2021:i:7854:d:10.1038_s41586-021-03417-2
DOI: 10.1038/s41586-021-03417-2
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Citations
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Cited by:
- Malmendier, Ulrike M. & Borgschulte, Mark & Guenzel, Marius & Liu, Canyao, 2020.
"CEO Stress, Aging, and Death,"
CEPR Discussion Papers
14933, C.E.P.R. Discussion Papers.
- Borgschulte, Mark & Guenzel, Marius & Liu, Canyao & Malmendier, Ulrike, 2023.
"CEO Stress, Aging, and Death,"
IZA Discussion Papers
16366, Institute of Labor Economics (IZA).
- Mark Borgschulte & Marius Guenzel & Canyao Liu & Ulrike Malmendier, 2021.
"CEO Stress, Aging, and Death,"
NBER Working Papers
28550, National Bureau of Economic Research, Inc.
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