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ERα promotes murine hematopoietic regeneration through the Ire1α-mediated unfolded protein response
- Source :
- eLife, eLife, Vol 7 (2018)
- Publication Year :
- 2018
- Publisher :
- eLife Sciences Publications, Ltd, 2018.
-
Abstract
- Activation of the unfolded protein response (UPR) sustains protein homeostasis (proteostasis) and plays a fundamental role in tissue maintenance and longevity of organisms. Long-range control of UPR activation has been demonstrated in invertebrates, but such mechanisms in mammals remain elusive. Here, we show that the female sex hormone estrogen regulates the UPR in hematopoietic stem cells (HSCs). Estrogen treatment increases the capacity of HSCs to regenerate the hematopoietic system upon transplantation and accelerates regeneration after irradiation. We found that estrogen signals through estrogen receptor α (ERα) expressed in hematopoietic cells to activate the protective Ire1α-Xbp1 branch of the UPR. Further, ERα-mediated activation of the Ire1α-Xbp1 pathway confers HSCs with resistance against proteotoxic stress and promotes regeneration. Our findings reveal a systemic mechanism through which HSC function is augmented for hematopoietic regeneration.
- Subjects :
- 0301 basic medicine
Mouse
QH301-705.5
medicine.drug_class
Science
Estrogen receptor
Ire1
Protein Serine-Threonine Kinases
Biology
General Biochemistry, Genetics and Molecular Biology
Mice
03 medical and health sciences
Endoribonucleases
estrogen
medicine
Animals
Biology (General)
Cells, Cultured
irradiation
General Immunology and Microbiology
General Neuroscience
Regeneration (biology)
Estrogen Receptor alpha
Estrogens
unfolded protein response
General Medicine
Hematopoietic Stem Cells
Cell biology
Transplantation
Haematopoiesis
Developmental Biology and Stem Cells
030104 developmental biology
Proteostasis
Estrogen
regeneration
Unfolded protein response
Medicine
Stem cell
Research Article
Signal Transduction
Subjects
Details
- ISSN :
- 2050084X
- Volume :
- 7
- Database :
- OpenAIRE
- Journal :
- eLife
- Accession number :
- edsair.doi.dedup.....668938b5e0a3deaff9e29218680c2bf5
- Full Text :
- https://doi.org/10.7554/elife.31159