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Blood, 1 June 2006, Vol. 107, No. 11, pp. 4326-4333.
Prepublished online as a Blood First Edition Paper on February 2, 2006; DOI 10.1182/blood-2005-11-4608.


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Submitted November 21, 2005
Accepted January 22, 2006

STAT5-induced self-renewal and impaired myelopoiesis of human hematopoietic stem/progenitor cells involves downmodulation of C/EBP{alpha}

Albertus T Wierenga, Hein Schepers, Malcolm A Moore, Edo Vellenga, and Jan Jacob Schuringa*

Department of Hematology, University Medical Center Groningen, Groningen, Groningen, The Netherlands
Developmental Hematopoiesis, Cell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA

* Corresponding author; email: j.schuringa{at}int.umcg.nl.

Previously, we demonstrated that enforced activation of STAT5A in human cord blood (CB)-derived stem/progenitor cells results in enhanced self-renewal and impaired myelopoiesis. The present study identifies C/EBP{alpha} as a critical component that is downregulated by STAT5. Microarray and RT-PCR analysis on STAT5A(1*6)-transduced CD34+ cells identified C/EBP{alpha} as the most prominently downregulated gene. To determine the cell-biological relevance of these observations, a 4-OHT-inducible C/EBP{alpha}-ER protein was co-expressed with the STAT5A(1*6) mutant in CB CD34+ cells using a retroviral approach. Re-expression of C/EBP{alpha} in STAT5A(1*6) cells resulted in a marked restoration of myelopoiesis. The proliferative advantage imposed on CD34+ cells by STAT5A(1*6) depended on the downmodulation of C/EBP{alpha} as reintroduction of C/EBP{alpha} induced a quick cell cycle arrest and the onset of myeloid differentiation. LTC-IC frequencies were elevated from 0.8±0.6% to 7.8±1.9% by STAT5A(1*6) as compared to controls, but these elevated LTC-IC frequencies were strongly reduced upon re-introduction of C/EBP{alpha} in STAT5A(1*6) cells and no 2nd CAFCs could be generated from double transduced cells. Enumeration of progenitors revealed that the number of CFCs was reduced over 20-fold when C/EBP{alpha} was co-expressed in STAT5A(1*6) cells. Our data indicate that downmodulation of C/EBP{alpha} is a prerequisite for STAT5-induced effects on self-renewal and myelopoiesis.


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