G-CSF-mobilized peripheral blood progenitor cells: In vitro growth pattern and hematopoietic growth factor receptor profile
Details
Publication Year 1997-04-01,Volume 25,Issue #4,Page 298-305
Journal Title
EXPERIMENTAL HEMATOLOGY
Publication Type
Journal Article
Abstract
The kinetics of colony formation by granulocyte colony-stimulating factor (G-CSF)-mobilized peripheral blood progenitor cells (PBPCs) were monitored using clone-mapping experiments. Compared with normal resting bone marrow (BM), where the ratio of Day 7:Day 14 granulocyte-macrophage colony-forming cells (GM-CFCs) was 1:0.76-1.9, PB was found to be relatively deficient in progenitor cells with the capacity to form colonies by Day 7 (median ratio Day 7:Day 14 1:21). The most mature Day 7 GM-CFCs, those dispersing or extinguishing before Day 14, were almost absent in PB (<1% of all GM-CFCs) but comprised 77% of Day 7 GM-CFCs and 32% of all GM-CFCs in BM. The expression patterns of high affinity receptors for G-CSF, GM-CSF, stem cell factor (SCF), and the ligand for flk-2 on CD38(hi) and CD38(-/dim) PB CD34(+) cells were determined by binding of I-125-labeled ligand and autoradiography. G-CSF receptor (G-CSFR) expression was detected on approximately 25% of CD38(-/dim) cells (estimated mean 105 receptors per positive cell) and was higher in CD38(hi) cells (approximately 50% positive, with a mean of 227 receptors per cell). GM-CSFR expression was low (approximately 25% of cells positive, mean of 120 receptors per cell) and did not vary with CD38 expression. c-kit (SCFR) and flk-2 were expressed by greater than or equal to 90% and greater than or equal to 80% of CD34(+) cells, respectively. SCF binding per cell was greater in the CD38(hi) population, while flk-2 expression did not vary with CD38 expression. These results confirm the heterogeneity of receptor expression by progenitor cells and imply differential regulation of receptor expression during maturation.
Publisher
CARDEN JENNINGS PUBL CO LTD
Keywords
COLONY-STIMULATING FACTOR; HIGH-DOSE CHEMOTHERAPY; UMBILICAL-CORD BLOOD; C-KIT RECEPTOR; BONE-MARROW; STEM-CELLS; PROLIFERATIVE CAPACITY; MONOCLONAL-ANTIBODY; HUMAN PROMYELOCYTES; CYTOKINE RECEPTORS
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 1997-04-01 12:00:00
An error has occurred. This application may no longer respond until reloaded. Reload 🗙