Effects of recombinant cytokines on colony formation by irradiated human cord blood CD34+ hematopoietic progenitor cells

Radiat Res. 1997 Jan;147(1):61-9.

Abstract

The role of recombinant hematopoietic growth factors in radiation repair has become a subject of increasing interest in both clinical and basic radiobiology. Combinations of cytokines such as hepatocyte growth factor, interleukin (IL)-3, IL-11, kit ligand, GM-CSF and erythropoietin were used to study the in vitro radiation dose response of human cord blood CD34+ hematopoietic progenitor cells using clonogenic survival assays. CD34+ cells were isolated by immunomagnetic selection and irradiated at 8 cGy/min. Irradiated cells were plated in methylcellulose with or without added cytokines, and hematopoietic colonies including CFU-GM, BFU-E and CFU-GEMM were scored on day 14. The radiation response characteristics of BFU-E and CFU-GEMM were similar for all culture conditions tested. The D0 values for BFU-E ranged between 1.29 and 2.40 Gy and n between 1.0 and 1.4. The D0 values for CFU-GEMM ranged from 86 cGy to 2.02 Gy and n between 1.0 and 1.5. The D0 for CFU-GM grown without added factors was 1.03 Gy. With single cytokine stimulation (IL-3, IL-11 or varying concentrations of HGF), D0 values ranged from 1.11 to 1.44 Gy. With the combination of IL-3, GM-CSF, kit ligand and HGF, D0 values were not significantly altered and ranged between 1.61 and 2.60 Gy. In contrast, the combination of IL-11 and HGF produced an increase in the shoulder of the radiation survival curve (n = 3.35). No increase in the shoulder was detected for any of the other conditions tested (n = 1.0-1.7). Thus the combination of HGF and IL-11 increased the radiation survival of hematopoietic progenitor cells forming CFU-GM. Understanding the mechanism by which combinations of early-acting growth factors support postirradiation recovery of primitive clonogenic hematopoietic cells may be relevant to the design of clinical protocols for improving hematopoietic recovery after total-body irradiation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, CD*
  • Antigens, CD34*
  • Cell Survival / drug effects
  • Cell Survival / radiation effects
  • Cells, Cultured
  • Cesium Radioisotopes
  • Colony-Forming Units Assay
  • Cytokines / pharmacology*
  • Dose-Response Relationship, Radiation
  • Drug Interactions
  • Erythropoietin / pharmacology
  • Fetal Blood
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / radiation effects*
  • Hepatocyte Growth Factor / pharmacology*
  • Humans
  • Interleukin-11 / pharmacology
  • Interleukin-3 / pharmacology
  • Kinetics
  • Recombinant Proteins / pharmacology
  • Stem Cell Factor / pharmacology
  • Time Factors

Substances

  • Antigens, CD
  • Antigens, CD34
  • Cesium Radioisotopes
  • Cytokines
  • Interleukin-11
  • Interleukin-3
  • Recombinant Proteins
  • Stem Cell Factor
  • Erythropoietin
  • Hepatocyte Growth Factor
  • Granulocyte-Macrophage Colony-Stimulating Factor