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Functional analysis of the homeobox gene HOXB4 in primitive hematopoietic cells

University of British Columbia

Hematopoiesis involves the ordered production of mature blood cells from a rare population of undifferentiated, totipotent, stem cells in the bone marrow. A pool of stem cells is preserved through self-renewing divisions, to maintain lifelong hematopoiesis. Deregulation of stem cell self-renewal and differentiation can have severe clinical consequences, including leukemia. Hematopoietic stem cells are also highly valuable for their therapeutic uses, as they can help reconstitute the hematopoietic system when transplanted. Yet despite the central importance of stem cells, we know very little about the regulatory mechanisms controlling their behaviour. HOXB4, a member of the Hox family of transcriptional regulators, was previously shown to selectively enhance hematopoietic stem cell growth in vivo. Hox family members have gene-specific roles in hematopoiesis, controlling differentiation and proliferation along specific lineages or even causing leukemia. Retrovirus-mediated overexpression of HOXB4 in murine bone marrow cells resulted in enhanced stem cell growth in vivo, without altering lympho-myeloid differentiation or predisposing to leukemia. The major objective of this thesis was to further explore the effects oiHOXB4 overexpression on primitive hematopoietic cells, and to test the utility and limitations of this strategy for stem cell expansion. Cells overexpressing HOXB4 had a competitive growth advantage in vitro, and a competitive transplant advantage in vivo. HOXB4 overexpressing bone marrow cell cultures showed increased proliferation over control cell cultures. Mice transplanted with //(9A34-transduced and control-transduced cells were selectively repopulated by the HOXB4 overexpressing cells. Importantly, the growth enhancement induced by HOXB4 overexpression did not come at the expense of normal differentiation. Further analysis of the //C7A7J4-mediated enhancement to stem cell expansion in vivo revealed that the rate of expansion was elevated. Accelerated stem cell regeneration mediated by HOXB4 allowed stem cell levels to reach 100% of pre-transplant levels within the first three months post-transplant. Stem cells did not expand beyond the normal level in HOXB4 mice, suggesting retained responsiveness to negative feedback mechanisms. Thus, //CTAB^-transduced stem cells remained responsive to positive and negative feedback on expansion and to differentiation-promoting signals. This work also addressed the potential for HOXB4 to serve as a stem cell expanding factor ex vivo. Although significant biological and clinical advances await effective stem cell expansion regimes, previous efforts have been largely unsuccessful. HOXB4 overexpression mediated rapid, extensive, and highly polyclonal stem cell expansions, resulting in over 1000-fold higher stem cell levels relative to controls and a 40-fold net stem cell expansion. These results show that HOXB4 can be used to expand stem cells ex vivo. The results presented in this thesis add to the recognition of Hox genes as important hematopoietic regulators. HOXB4 in particular can play a key role in the regulation of the rate and/or probability of hematopoietic stem cell self-renewal. These studies further suggest the complex biomolecular pathways controlling stem cell fate, and point to new avenues to manipulate HSC expansion.

Thesis/Dissertation

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2009-09-22

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http://hdl.handle.net/2429/13004

Genetics

University of British Columbia

UBCV

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