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• W2023168194 abstract "<h3>ABSTRACT</h3> Reconstitution after hematopoietic stem cell (HSC) transplantation is assumed to occur in two distinct phases: initial recovery mediated by short-term progenitors and long-term repopulation by multipotent HSCs which do not contribute to hematopoietic reconstitution during the first 6-9 months. We have previously reported the transplantation and exclusive engraftment of the HSC-enriched CD34⁺CD45RA^-CD90⁺ phenotype in a nonhuman primate model. Here, we closely followed the clonal diversity and kinetics in these animals. Enhanced sampling and high density clonal tracking within the first 3 month revealed that multipotent HSCs actively contributed to the early phases of neutrophil recovery and became the dominant source for blood cells as early as 50 days after transplant. Longitudinal changes in clonal diversity supported a stochastic engraftment of HSCs with the majority of HSCs clones vanishing early during neutrophil recovery and a smaller fraction of HSC clones expanding into bigger pools to support long-term hematopoiesis. In contrast to the bi-phasic model, we propose that hematopoietic recovery after myeloablation and transplantation is primarily derived from HSCs in a stochastic manner rather than in two phases by independent cell populations." @default.
• W2023168194 created "2016-06-24" @default.
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• W2023168194 date "2009-10-21" @default.
• W2023168194 modified "2023-10-03" @default.
• W2023168194 title "Age, Alzheimer disease, and brain structure" @default.
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• W2023168194 doi "https://doi.org/10.1212/wnl.0b013e3181c3f293" @default.
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