The mammalian Hox genes encode a family of conserved transcription factors
that control the establishment of the body plan during embryogenesis. Many
Hox genes are also known to be expressed in hematopoietic cells. We found t
hat Hoxc-8, a member of the Hox C cluster, is expressed in the mouse hemato
poietic organs, fetal liver and adult bone marrow. To determine the role of
Hoxc-8 gene in hematopoiesis, we compared progenitor cell numbers in the f
etal liver and adult bone marrow cells. We observed a significant reduction
in the number of erythroid burst-forming unit (BFU-E) and in granulocyte/m
acrophage colony-forming unit (CFU-GM) in the Hoxc-8 null mice, although th
e peripheral blood cell counts were normal. The hematopoietic cells from th
e homozygote animals exhibited normal expansion capability in a liquid cult
ure system, suggesting that the decreased number of progenitor cells may be
due to a defect extrinsic to the hematopoietic cells, such as in the inter
action with the microenvironment. J. Exp. Zool. 283:186-193, 1999. (C) 1999
Wiley-Liss, Inc.