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  Clonal expansion capacity defines two consecutive developmental stages of long-term hematopoietic stem cells.

Grinenko, T., Arndt, K., Portz, M., Mende, N., Günther, M., Cosgun, K. N., et al. (2014). Clonal expansion capacity defines two consecutive developmental stages of long-term hematopoietic stem cells. The Journal of Experimental Medicine, 211(2), 209-215.

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 Creators:
Grinenko, Tatyana, Author
Arndt, Kathrin, Author
Portz, Melanie1, Author
Mende, Nicole, Author
Günther, Marko, Author
Cosgun, Kadriye Nehir, Author
Alexopoulou, Dimitra, Author
Lakshmanaperumal, Naharajan2, Author           
Henry, Ian2, Author           
Dahl, Andreas1, Author
Waskow, Claudia1, Author
Affiliations:
1Max Planck Society, ou_persistent13              
2Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Abstract: Long-term hematopoietic stem cells (HSCs [LT-HSCs]) are well known to display unpredictable differences in their clonal expansion capacities after transplantation. Here, by analyzing the cellular output after transplantation of stem cells differing in surface expression levels of the Kit receptor, we show that LT-HSCs can be systematically subdivided into two subtypes with distinct reconstitution behavior. LT-HSCs expressing intermediate levels of Kit receptor (Kit(int)) are quiescent in situ but proliferate extensively after transplantation and therefore repopulate large parts of the recipient's hematopoietic system. In contrast, metabolically active Kit(hi) LT-HSCs display more limited expansion capacities and show reduced but robust levels of repopulation after transfer. Transplantation into secondary and tertiary recipient mice show maintenance of efficient repopulation capacities of Kit(int) but not of Kit(hi) LT-HSCs. Initiation of differentiation is marked by the transit from Kit(int) to Kit(hi) HSCs, both of which precede any other known stem cell population.

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 Dates: 2014
 Publication Status: Issued
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 Identifiers: eDoc: 705760
Other: 5652
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Title: The Journal of Experimental Medicine
Source Genre: Journal
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Pages: - Volume / Issue: 211 (2) Sequence Number: - Start / End Page: 209 - 215 Identifier: -