Title
Analysis of expansion of myeloid progenitors in mice to identify leukemic susceptibility genes
Document Type
Article
Publication Date
Winter 3-23-2006
Abstract
The myeloid progenitor cell compartment (MPC) exhibits pronounced expansion in human myeloid leukemias. It is becoming more apparent that progression of myelodysplastic syndromes and myeloproliferative diseases to acute myelogenous leukemia is the result of defects in progenitor cell maturation. The MPC of bone marrow was analyzed in mice using a cell culture assay for measuring the relative frequency of proliferative myeloid progenitors. Response to the cytokines SCF, IL-3, and GMCSF was determined by this assay for the leukemic mouse strain BXH-2 and ten other inbred mouse strains. Significant differences were found to exist among ten inbred mouse strains in the nature of their MPC in bone marrow, indicating the presence of genetic polymorphisms responsible for the divergence. The SWR/J and FVB/J strains show consistently low frequencies of myeloid progenitors, while the DBA/2J and SJL/J inbred strains show consistently high frequencies of myeloid progenitors within the bone marrow compartment. In addition, in silico linkage disequilibrium analysis was conducted to identify possible chromosomal regions responsible for the phenotypic variation. Given the importance of this cell compartment in leukemia progression and the soon to be released genomic sequence of 15 mouse strains, these differences may provide a valuable tool for research into leukemia.
Recommended Citation
Sollars VE, Pequignot E, Rothstein JL, Buchberg AM: Analysis of expansion of myeloid progenitors in mice to identify leukemic susceptibility genes. Mamm Genome 2006, 17(8):808-821.
Comments
This article first appeared in Volume 35, Number 3 of Evolutionary Biology. Dominy NJ, Vogel ER, Yeakel JD, Constantino P, and Lucas PW. The mechanical properties of plant underground storage organs and implications for the adaptive radiation and resource partitioning of early hominins. Evolutionary Biology 35(3): 159-175., and is reprinted with permission. The final publication is available at http://www.springerlink.com