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Long-Term Propagation of Distinct Hematopoietic Differentiation Programs In Vivo
Abstract
Heterogeneity in the differentiation behavior of hematopoietic stem cells is well documented but poorly understood. To investigate this question at a clonal level, we isolated a subpopulation of adult mouse bone marrow that is highly enriched for multilineage in vivo repopulating cells and transplanted these as single cells, or their short-term clonal progeny generated in vitro, into 352 recipients. Of the mice, 93 showed a donor-derived contribution to the circulating white blood cells for at least 4 months in one of four distinct patterns. Serial transplantation experiments indicated that two of the patterns were associated with extensive self-renewal of the original cell transplanted. However, within 4 days in vitro, the repopulation patterns subsequently obtained in vivo shifted in a clone-specific fashion to those with less myeloid contribution. Thus, primitive hematopoietic cells can maintain distinct repopulation properties upon serial transplantation in vivo, although these properties can also alter rapidly in vitro.
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“Most T cells and B cells belonged to lymphoid-dominated (LARRY and EPI-Clone) clones (Fig. 2i and Supplementary Fig. 4d), which implicated an origin in lymphoid-biased or restricted progenitors30.”
From Clonal tracing with somatic epimutations reveals dynamics of blood ageing (2025) · cites this paper as [30]
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“which implicated an origin in lymphoid-biased or restricted progenitors30.”
From Clonal tracing with somatic epimutations reveals dynamics of blood ageing (2025) · cites this paper as [30]
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Bmi-1 is required for maintenance of adult self-renewing haematopoietic stem cells.
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“Several studies suggest that cells with a differentiation characteristics may increase as mice age (Sudo et al., 2000; Kim et al., 2003; Rossi et al., 2005; Liang et al., 2005).”
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Metadata
- Authors
- Dykstra, B., Kent, D., Bowie, M., McCaffrey, L., Hamilton, M., Lyons, K., Lee, S.-J., Brinkman, R., & Eaves, C.
- Venue
- Cell Stem Cell
- Publisher
- Elsevier BV
- Published
- 2007-08
- Volume
- 1
- Issue
- 2
- Pages
- 218-229
- ISSN
- 1934-5909
- Cited by
- 609
- References
- 2
- Language
- en
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