Increased recruitment of hematopoietic progenitor cells underlies the ex vivo expansion potential of FLT3 ligand

• Published in: Blood Vol. 90; no. 6; pp. 2260 - 2272
• Main Authors: HAYLOCK, D. N, HORSFALL, M. J, SIMMONS, P. J, DOWSE, T. L, RAMSHAW, H. S, NIUTTA, S, PROTOPSALTIS, S, PENG, L, BURRELL, C, RAPPOLD, I, BUHRING, H.-J
• Format: Journal Article
• Language: English
• Published: Washington, DC The Americain Society of Hematology 15.09.1997
• Subjects: ADP-ribosyl Cyclase; ADP-ribosyl Cyclase 1; Adult; Antigens, CD; Antigens, CD34 - analysis; Antigens, Differentiation - analysis; Biological and medical sciences; Bone Marrow Cells; Cell Cycle; Cell differentiation, maturation, development, hematopoiesis; Cell physiology; Cell Separation; Cells, Cultured; Erythropoiesis; Flow Cytometry; fms-Like Tyrosine Kinase 3; Fundamental and applied biological sciences. Psychology; Hematopoiesis; Hematopoietic Cell Growth Factors - physiology; Hematopoietic Stem Cells - cytology; Hematopoietic Stem Cells - physiology; Humans; Immunophenotyping; Membrane Glycoproteins; Membrane Proteins - physiology; Molecular and cellular biology; NAD+ Nucleosidase - analysis; Proto-Oncogene Proteins - physiology; Receptor Protein-Tyrosine Kinases - physiology; Retroviridae - genetics; Transduction, Genetic; Human; Cell proliferation; Cell culture; Granulocyte colony stimulating factor; Ex vivo; Polypeptide; Stem cell; Cytokine; Hematopoietic cell; Mast cell growth factor
• DOI: 10.1182/blood.v90.6.2260
• ISSN: 0006-4971

The ligand for flt-3 (FLT3L) exhibits striking structural homology with stem cell factor (SCF) and monocyte colony-stimulating factor (M-CSF) and also acts in synergy with a range of other hematopoietic growth factors (HGF). In this study, we show that FLT3L responsive hematopoietic progenitor cells (HPC) are CD34+CD38-, rhodamine 123dull, and hydroperoxycyclophosphamide (4-HC) resistant. To investigate the basis for the capacity of FLT3L to augment the de novo generation of myeloid progenitors from CD34+CD38- cells, single bone marrow CD34+CD38- cells were sorted into Terasaki wells containing serum-free medium supplemented with interleukin-3 (IL-3), IL-6, granulocyte colony-stimulating factor (G-CSF), SCF (4 HGF) +/- FLT3L. Under these conditions, FLT3L recruited approximately twofold more CD34+CD38- cells into division than 4 HGF alone. The enhanced proliferative response to FLT3L was evident by day 3 and was maintained at all subsequent time points examined. In accord with these findings, we also show that transduction of CD34+CD38- cells with the LAPSN retrovirus is enhanced by FLT3L. The results of these experiments therefore indicate that increased recruitment of primitive HPC into cell cycle underlies the ex vivo expansion potential of FLT3L and also its ability to improve retroviral transduction of HPC.