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August 2001, Volume 15, Number 8, Pages 1203-1216
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Original Manuscript
Enhanced ability of daniplestim and myelopoietin-1 to suppress apoptosis in human hematopoietic cells
J A McCubrey1,2, W L Blalock1, O Saleh1, M Pearce1, C Burrows1, L S Steelman1, J T Lee1, R A Franklin1,2, S M Oberhaus2,1, P W Moye1, P D Doshi3 and J P McKearn3

1Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University, Greenville, NC 27858, USA

2Leo Jenkins Cancer Center, Brody School of Medicine at East Carolina University, Greenville, NC 27858, USA

3Pharmacia Corporation, St Louis, MO 63198, USA

Correspondence to: J A McCubrey, Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University, Greenville, NC 27858, USA; Fax: (252)-816-3104

Abstract

Modified and chimeric cytokines have been developed to aid in the recovery of hematopoietic precursor cells after myeloablative chemotherapy. The interleukin-3 (IL-3) receptor agonist, daniplestim, binds to the IL-3 receptor-alpha subunit with 60-fold greater affinity and induces cell proliferation and colony-forming unit formation 10- to 22-fold better than native IL-3. A chimeric cytokine, myelopoietin-1, composed of daniplestim and a G-CSF receptor agonist binds both the IL-3 and G-CSF receptors. While the in vivo effects of daniplestim and myelopoietin-1 are well described, the mechanisms by which they stimulate growth are not well understood. We have investigated the effects of daniplestim and myelopoietin-1 on the prevention of apoptosis in two human hematopoietic cell lines, OCI-AML.5 and AML 193. Daniplestim and myelopoietin-1 prevented apoptosis to a greater degree than native recombinant IL-3 or G-CSF as determined by annexin V/propidium iodide binding and TUNEL assays. Daniplestim and myelopoietin-1 promoted the maintenance of the mitochondrial membrane potential better than native IL-3 or G-CSF. These cytokines promoted a lower redox potential as higher levels of free radicals were detected after cytokine treatment than in cytokine-deprived cells implying increased respiration. These results indicate that daniplestim and myelopoietin-1 are able to prevent apoptosis in hematopoietic cells more effectively than native IL-3 and G-CSF. These effects of daniplestim and myelopoietin-1 may contribute to their effective ability to repopulate hematopoietic precursor cells after chemotherapy. Leukemia (2001) 15, 1203-1216.

Keywords

apoptosis; cytokines; redox potential; signal transduction

Received 12 January 2001; accepted 27 March 2001
August 2001, Volume 15, Number 8, Pages 1203-1216
Table of contents    Previous  Abstract  Next   Full text  PDF
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