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A bone marrow stromal cell line is a source and target for platelet-
derived growth factor
SL Abboud
Department of Medicine, University of Texas Health Science Center, San
Antonio 78284.
Platelet-derived growth factor (PDGF) stimulates multipotent and erythroid
progenitors as well as stromal fibroblasts. Any of the three dimeric forms
of PDGF (AA, AB, or BB) could potentially interact with these cells;
however, the precise cellular origin of PDGF production in the bone marrow
microenvironment is not known. In the present study, we found that medium
conditioned by MBA-2, murine bone marrow-derived endothelial cells,
contains PDGF activity that competes for [125I]PDGF binding to human
foreskin fibroblasts and is mitogenic for these fibroblasts. Northern
analysis of poly(A)+ RNA from MBA-2 shows the expression of both PDGF
A-chain and B-chain mRNAs. Because cytokines such as transforming growth
factor-beta (TGF-beta) regulate hematopoiesis and stimulate PDGF in certain
mesenchymal cells, we determined whether TGF-beta influences PDGF secretion
and gene expression in MBA-2. TGF-beta induced PDGF A-chain and B-chain
mRNAs and the release of PDGF activity. Each of the three PDGF isoforms
also stimulated DNA synthesis in MBA-2, but with different potency (BB >
AB > AA). Ligand binding studies showed specific binding of labeled PDGF
BB and, to a lesser extent, PDGF AA isoform, consistent with predominant
expression of the PDGF-beta receptor in MBA-2. These data show that murine
endothelial stromal cells release PDGF activity and respond to PDGF. Local
production of PDGF in the marrow microenvironment may play an important
role in regulating hematopoietic and stromal cell proliferation.
Volume 81,
Issue 10,
pp. 2547-2553,
05/15/1993
Copyright © 1993 by The American Society of Hematology

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