Intermediate-term Hematopoietic Stem Cells with Extended but Time-limited Reconstitution Potential
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Sustained blood cell production depends on divisions by hematopoietic stem cells (HSCs) that yield both differentiating progeny as well as new HSCs via self-renewal. Differentiating progeny remain capable of self-renewal, but only HSCs sustain self-renewal through successive divisions securely enough to maintain clones that persist life-long. Until recently, the first identified next stage consisted of "short-term" reconstituting cells able to sustain clones of differentiating cells for only 4-6 weeks. Here we expand evidence for a numerically dominant "intermediate-term" multipotent HSC stage in mice whose clones persist for 6-8 months before becoming extinct and that are separable from both short-term as well as permanently reconstituting "long-term" HSCs. The findings suggest that the first step in stem cell differentiation consists not in loss of initial capacity for serial self-renewal divisions, but rather in loss of mechanisms that stabilize self-renewing behavior throughout successive future stem cell divisions.
STOCHASTIC MODELING OF HEMATOPOIETIC STEM CELL DYNAMICS.
Alfaro-Quinde C, Krstanovic K, Vasquez P, Kathrein K bioRxiv. 2025; .
PMID: 39974985 PMC: 11838373. DOI: 10.1101/2025.01.27.635091.
Watt S, Roubelakis M Int J Mol Sci. 2025; 26(2).
PMID: 39859383 PMC: 11766050. DOI: 10.3390/ijms26020671.
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Morales-Hernandez A, Kooienga E, Sheppard H, Gheorghe G, Caprio C, Chabot A Hemasphere. 2024; 8(11):e70037.
PMID: 39479518 PMC: 11522827. DOI: 10.1002/hem3.70037.
Boutzen H, Murison A, Oriecuia A, Bansal S, Arlidge C, Wang J Leukemia. 2024; 38(10):2090-2101.
PMID: 39169113 PMC: 11436360. DOI: 10.1038/s41375-024-02358-9.
DNA fork remodeling proteins, Zranb3 and Smarcal1, are uniquely essential for aging hematopoiesis.
Kushinsky S, Puccetti M, Adams C, Shkundina I, James N, Mahon B Aging Cell. 2024; 23(11):e14281.
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