Abstract:
:The switch from fetal to adult hematopoietic stem/progenitor cells (HSPCs) is associated with profound changes in several genetic programs. Although HSPC ageing corresponds to alterations in Wnt signaling, relatively little is known about the relative roles of different Wnt signaling pathways in HSPC ontogeny. We hypothesized that proliferating fetal HSPCs would be more dependent on canonical β-catenin-dependent Wnt signaling when compared to quiescent adult bone marrow HSPCs. We have compared here Wnt signaling activities in murine fetal and adult HSPCs and demonstrate a shift from Wnt/β-catenin-dependent signaling in fetal liver HSPCs to more predominantly noncanonical Wnt/polarity signaling in adult HSPCs. β-Catenin was selectively required for fetal HSPC competitiveness shortly after transplant, and protected cells from oxidative stress. Our results emphasize the complexity of Wnt signaling dynamics in HSPC maintenance and function.
journal_name
J Leukoc Bioljournal_title
Journal of leukocyte biologyauthors
Kwarteng EO,Hétu-Arbour R,Heinonen KMdoi
10.1002/JLB.1HI0917-373Rsubject
Has Abstractpub_date
2018-03-01 00:00:00pages
381-393issue
3eissn
0741-5400issn
1938-3673journal_volume
103pub_type
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