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PMID: 11238087 Published · ppublish English Comparative Study Journal Article

Rapid mobilization of murine hematopoietic stem cells with enhanced engraftment properties and evaluation of hematopoietic progenitor cell mobilization in rhesus monkeys by a single injection of SB-251353, a specific truncated form of the human CXC chemokine GRObeta.

Blood ·Vol. 97 ·No. 6 ·2001-03-15 ·Pages 1534-42

King AG, Horowitz D, Dillon SB, Levin R, Farese AM, MacVittie TJ, Pelus LM

Abstract

SB-251353 is an N-terminal truncated form of the human CXC chemokine GRObeta. Recombinant SB-251353 was profiled in murine and rhesus monkey peripheral blood stem cell mobilization and transplantation models. SB-251353 rapidly and transiently mobilized hematopoietic stem cells and neutrophils into the peripheral blood after a single subcutaneous injection. Transplantation of equivalent numbers of hematopoietic stem cells mobilized by SB-251353 into lethally irradiated mice resulted in faster neutrophil and platelet recovery than stem cells mobilized by granulocyte colony-stimulating factor (G-CSF). A single injection of SB-251353 in combination with 4 days of G-CSF administration resulted in augmented stem and progenitor cell mobilization 5-fold greater than G-CSF alone. Augmented stem cell mobilization could also be demonstrated in mice when a single injection of SB-251353 was administered with only one-day treatment with G-CSF. In addition, SB-251353, when used as a single agent or in combination with G-CSF, mobilized long-term repopulating stem cells capable of hematopoietic reconstitution of lethally irradiated mice. In rhesus monkeys, a single injection of SB-251353 induced rapid increases in peripheral blood hematopoietic progenitor cells at a 50-fold lower dose than in mice, which indicates a shift in potency. These studies provide evidence that the use of SB-251353 alone or in combination with G-CSF mobilizes hematopoietic stem cells with long-term repopulating ability. In addition, this treatment may (1) reduce the number of apheresis sessions and/or amount of G-CSF required to collect adequate numbers of hematopoietic stem cells for successful peripheral blood cell transplantation and (2) improve hematopoietic recovery after transplantation.

MeSH Terms
Animals Blood Platelets/cytology,drug effects Chemokine CXCL1 Chemokine CXCL2 Chemokines, CXC/administration & dosage,pharmacology,physiology,therapeutic use Chemotactic Factors/administration & dosage,pharmacology,physiology,therapeutic use Drug Therapy, Combination Granulocyte Colony-Stimulating Factor/therapeutic use Growth Substances/pharmacology,physiology,therapeutic use Hematopoiesis/drug effects Hematopoietic Stem Cell Mobilization/methods,standards Hematopoietic Stem Cell Transplantation/methods,standards Hematopoietic Stem Cells/drug effects Humans Intercellular Signaling Peptides and Proteins Macaca mulatta Male Matrix Metalloproteinase 9/metabolism,pharmacology Mice Mice, Inbred C57BL Models, Animal Neoplasm Proteins/pharmacology,physiology,therapeutic use Neutrophils/cytology,drug effects Species Specificity
Chemicals
CXCL1 protein, human CXCL2 protein, human Chemokine CXCL1 Chemokine CXCL2 Chemokines, CXC Chemotactic Factors Cxcl1 protein, mouse Growth Substances Intercellular Signaling Peptides and Proteins Neoplasm Proteins Granulocyte Colony-Stimulating Factor Matrix Metalloproteinase 9 SB251353
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
King A G
Department of Molecular Virology and Host Defense, SmithKline Beecham Pharmaceuticals, Collegeville, PA 19426-0989, USA. andrew_g_king@sbphrd.com
Horowitz D
Dillon S B
Levin R
Farese A M
MacVittie T J
Pelus L M
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2001-03-15
Pages
1534-42
Language
English
Region
United States
NLM ID
7603509
Subset
IM
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