TUMOR-NECROSIS-FACTOR-ALPHA INHIBITS STEM-CELL FACTOR-INDUCED PROLIFERATION OF HUMAN BONE-MARROW PROGENITOR CELLS IN-VITRO - ROLE OF P55 AND P75 TUMOR-NECROSIS-FACTOR RECEPTORS

Citation
Ls. Rusten et al., TUMOR-NECROSIS-FACTOR-ALPHA INHIBITS STEM-CELL FACTOR-INDUCED PROLIFERATION OF HUMAN BONE-MARROW PROGENITOR CELLS IN-VITRO - ROLE OF P55 AND P75 TUMOR-NECROSIS-FACTOR RECEPTORS, The Journal of clinical investigation, 94(1), 1994, pp. 165-172
Citations number
67
Categorie Soggetti
Medicine, Research & Experimental
ISSN journal
00219738
Volume
94
Issue
1
Year of publication
1994
Pages
165 - 172
Database
ISI
SICI code
0021-9738(1994)94:1<165:TISFP>2.0.ZU;2-Y
Abstract
Stem cell factor (SCF), a key regulator of hematopoiesis, potently syn ergizes with a number of hematopoietic growth factors. However, little is known about growth factors capable of inhibiting the actions of SC F. TNF-alpha has been shown to act as a bidirectional regulator of mye loid cell proliferation and differentiation This study was designed to examine interactions between TNF-alpha and SCF. Here, we demonstrate that TNF-alpha potently and directly inhibits SCF-stimulated prolifera tion of CD34(+) hematopoietic progenitor cells. Furthermore, TNF-alpha blocked all colony formation stimulated by SCF in combination with gr anulocyte colony-stimulating factor (CSF) or CSF-1. The synergistic ef fect of SCF observed in combination with GM-CSF or IL-3 was also inhib ited by TNF-alpha, resulting in colony numbers similar to those obtain ed in the absence of SCF. These effects of TNF-alpha were mediated thr ough the p55 TNF receptor, whereas little or no inhibition was signale d through the p75 TNF receptor. Finally, TNF-alpha downregulated c-kit cell-surface expression on CD34(+) bone marrow cells, and this was pr edominantly a p55 TNF receptor-mediated event as well.