Back to Search Start Over

Specific plasma membrane protein phenotype of culture-amplified and native human bone marrow mesenchymal stem cells

Authors :
Pierre Layrolle
Nathalie Gallay
Dominique Kerboeuf
Jochen Ringe
Philippe Rosset
Luc Sensebé
Pierre Charbord
Bruno Delorme
Christian Jorgensen
Yves Le Vern
Thomas Häupl
Institut National de la Santé et de la Recherche Médicale (INSERM)
Charité - UniversitätsMedizin = Charité - University Hospital [Berlin]
Infectiologie Animale et Santé Publique (UR IASP)
Institut National de la Recherche Agronomique (INRA)
U844
Centre Hospitalier Régional Universitaire de Tours (CHRU de Tours)
Etablissement Français du Sang
U791
Institut Naltional de la Santé et de la Recherche Médicale
Source :
Blood, Blood, American Society of Hematology, 2008, 111 (5), pp.2631-2635. ⟨10.1182/blood-2007-07-099622⟩
Publication Year :
2008
Publisher :
American Society of Hematology, 2008.

Abstract

International audience; We have studied the plasma membrane protein phenotype of human culture-amplified and native bone marrow mesenchymal stem cells (BM MSCs). We have found, using microarrays and flow cytometry, that cultured cells express specifically 113 transcripts and 17 proteins that were not detected in hematopoietic cells. These antigens define a lineage-homogenous cell population of mesenchymal cells, clearly distinct from the hematopoietic lineages, and distinguishable from other cultured skeletal mesenchymal cells (periosteal cells and synovial fibroblasts). Among the specific membrane proteins present on cultured MSCs, 9 allowed the isolation from BM mononuclear cells of a minute population of native MSCs. The enrichment in colony-forming units–fibroblasts was low for CD49b, CD90, and CD105, but high for CD73, CD130, CD146, CD200, and integrin alphaV/beta5. In addition, the expression of CD73, CD146, and CD200 was down-regulated in differentiated cells. The new marker CD200, because of its specificity and immunomodulatory properties, deserves further in-depth studies.

Details

ISSN :
15280020 and 00064971
Volume :
111
Database :
OpenAIRE
Journal :
Blood
Accession number :
edsair.doi.dedup.....d83de78121e2287267aad7b21b340b43