Literature DB >> 18086871

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

Bruno Delorme1, Jochen Ringe, Nathalie Gallay, Yves Le Vern, Dominique Kerboeuf, Christian Jorgensen, Philippe Rosset, Luc Sensebé, Pierre Layrolle, Thomas Häupl, Pierre Charbord.   

Abstract

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.

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Year:  2007        PMID: 18086871     DOI: 10.1182/blood-2007-07-099622

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  95 in total

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9.  Multi-peptide presentation and hydrogel mechanics jointly enhance therapeutic duo-potential of entrapped stromal cells.

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