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Blood, 1 April 2001, Vol. 97, No. 7, pp. 1968-1974

HEMATOPOIESIS

Erythroblasts are a source of angiogenic factors

Rafaèle Tordjman, Stéphanie Delaire, Jean Plouët, Stephen Ting, Philippe Gaulard, Serge Fichelson, Paul-Henri Roméo, and Valérie Lemarchandel

From Institut National de la Santé et de la Recherche Médicale (INSERM) U474, Maternité Port-Royal, and Laboratoire d'Hématopoïèse, Site Transfusionnel, Hôpital Cochin, Paris, France; INSERM U448 and Département de Pathologie EA 2348, Hôpital Mondor, Créteil, France; IPBS, GDR 1927, Centre National de la Recherche Scientifique UPR 9062, Toulouse, France.

In adult bone marrow, mature erythroblasts are produced within structures called erythroblastic islands and then cross the endothelial barrier to reach circulation. Erythroblastic islands are composed of a central macrophage surrounded by maturing erythroblasts. In this study, it is shown that erythroid cells, but not the other mature hematopoietic cells, coexpress 2 angiogenic factors, vascular endothelial growth factor A (VEGF-A) and placenta growth factor (PlGF). Secretion of both VEGF-A and PlGF increases during in vitro erythroid differentiation. Erythroblast-conditioned medium can induce both migration of monocytes and endothelial cells and the permeability of endothelial cells. These effects are inhibited by anti-PlGF and/or anti-VEGF antibodies. Finally, it is shown that VEGF-A and PlGF proteins are expressed by bone marrow erythroblasts in vivo. Angiogenic factors secreted by erythroblasts may promote interactions either with macrophages in erythroblastic islands or with endothelial cells that would facilitate the passage of erythroid cells through the endothelial barrier.

© 2001 by The American Society of Hematology.
 

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