Journal
BLOOD
Volume 127, Issue 15, Pages 1881-1885Publisher
AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2015-09-666974
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Funding
- Fondation de France [201200029166]
- Fondation pour la Recherche Medicale grant [INE201000518534]
- Fondation ARC pour la recherche sur le cancer
- Canceropole Provence-Alpes-Cote d'Azur
- Ligue Nationale Contre le Cancer
- Institut Thematique Multi-Organismes Cancer
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Hematopoietic stem cells (HSCs) give rise to all blood populations due to their longterm self-renewal and multipotent differentiation capacities. Because they have to persist throughout an organism's life span, HSCs tightly regulate the balance between proliferation and quiescence. Here, we investigated the role of the transcription factor promyelocytic leukemia zinc finger (plzf) in HSC fate using the Zbtb16(lu/lu) mouse model, which harbors a natural spontaneous mutation that inactivates plzf. Regenerative stress revealed that Zbtb16(lu/lu) HSCs had a lineage-skewing potential from lymphopoiesis toward myelopoiesis, an increase in the long-term HSC pool, and a decreased repopulation potential. Furthermore, old plzf-mutant HSCs present an amplified aging phenotype, suggesting that plzf controls age-related pathway. We found that Zbtb16(lu/lu) HSCs harbor a transcriptional signature associated with a loss of stemness and cell cycle deregulation. Lastly, cell cycle analyses revealed an important role for plzf in the regulation of the G1-S transition of HSCs. Our study reveals a new role for plzf in regulating HSC function that is linked to cell cycle regulation, and positions plzf as a key player in controlling HSC homeostasis.
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