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- PMID: 12082538
- UKPMCID: 12082538
- DOI: 10.1038/sj.onc.1205424
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BCR-ABL alters the proliferation and differentiation response of multipotent hematopoietic cells to stem cell factor.
Pierce, Andrew; Spooncer, Elaine; Ainsworth, Shaun; Whetton, Anthony D
Oncogene. 2002;21(19):3068-75.
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Full-text held externally
- PMID: 12082538
- UKPMCID: 12082538
- DOI: 10.1038/sj.onc.1205424
Abstract
Chronic myeloid leukaemia (CML), a hematopoietic stem cell disorder is characterized by the expression of BCR-ABL. To investigate the effects of BCR-ABL on multipotent hematopoietic cells, a temperature sensitive BCR-ABL tyrosine kinase was expressed in the cell line, FDCP-Mix. BCR-ABL mediated an increase in c-kit expression that correlated with an enhanced mitogenic response to SCF. This was not observed in the absence of Bcr-Abl kinase activity or presence of the BCR-ABL inhibitor STI571, which also inhibits c-kit. When cultured in a combination of SCF plus G-CSF the FDCP-Mix cells undergo neutrophilic differentiation over a 7-10 day period. When BCR-ABL was active there was a marked inhibition of cell maturation compared to control cells in which BCR-ABL was either inactive or not present. However, BCR-ABL did not block differentiation as the cells eventually undergo terminal maturation. These data argue that BCR-ABL is directly responsible for the enhanced response to SCF reported in CML progenitor cells. Furthermore, although the primary effect of STI571 is via direct inhibition of BCR-ABL, STI571 additionally reduces the enhanced response to SCF. Thus there are two sites of STI571 action of potential importance in Bcr-Abl expressing cells.