Differential effects of fibroblast growth factor-4, epidermal growth factor and transforming growth factor-beta1 on

Ki-Ryang Koh1, Kensuke Ohta, Hirohisa Nakamae

  • 1Clinical Hematology and Clinical Diagnostics, Graduate School of Medicine, Osaka City University, 1-4-3, Asahimachi, Abeno-ku, Osaka, Japan.

Leukemia Research
|August 7, 2002
PubMed

Insights

Fibroblast growth factor-4 (FGF-4) enhanced hematopoietic support in stromal cells, while transforming growth factor-beta1 (TGF-beta1) impaired it. These growth factors differentially impact leukemic and normal stromal cell function.

Area of Science:

  • Hematology
  • Cell Biology
  • Cancer Research

Background:

  • Stromal cells in bone marrow support hematopoietic cell development.
  • This supportive function is impaired in stromal layers from acute myeloid leukemia (AML) patients.
  • Growth factors may influence the functional development of these stromal layers.

Purpose of the Study:

  • To investigate the effects of fibroblast growth factor-4 (FGF-4), epidermal growth factor (EGF), and transforming growth factor-beta1 (TGF-beta1) on leukemic stromal layer function.
  • To determine if these growth factors can modify the hematopoietic supporting abilities of stromal cells.

Main Methods:

  • Stromal layers were established from 13 AML patients and 6 controls.
  • Cells were treated with FGF-4, EGF, or TGF-beta1.
  • Hematopoietic progenitor cell output was assessed using colony-forming assays after co-culture with CD34+ cells.

Main Results:

  • FGF-4 significantly increased progenitor cell output in both leukemic and non-leukemic stromal cells compared to controls.
  • TGF-beta1 significantly decreased progenitor cell output.
  • EGF did not significantly alter progenitor cell output.
  • Observed differences were significant after 4 weeks, suggesting an impact on primitive progenitors.

Conclusions:

  • FGF-4 enhances the hematopoietic supportive function of stromal layers.
  • TGF-beta1 impairs this function.
  • FGF-4 and TGF-beta1 differentially modulate the functional development of both normal and leukemic stromal layers.

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