Changes in surface markers of human mesenchymal stem cells during the chondrogenic differentiation and dedifferentiation processes in vitro
Author(s) -
Lee Hyun Jung,
Choi Byung Hyune,
Min ByoungHyun,
Park So Ra
Publication year - 2009
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.24786
Subject(s) - mesenchymal stem cell , chondrogenesis , antigen , cd44 , cd90 , microbiology and biotechnology , chemistry , cellular differentiation , cluster of differentiation , in vitro , flow cytometry , immunology , biology , cell , biochemistry , gene
Objective To investigate surface markers showing specific changes during the chondrogenic differentiation and dedifferentiation of human mesenchymal stem cells (MSCs). Methods Human MSCs from adult bone marrow were subjected to chondrogenic differentiation in 3‐dimensional (3‐D) alginate culture with or without transforming growth factor β3 (TGFβ3) for 2 weeks, followed by dedifferentiation in monolayer for 1 week. Surface antigens were selected from those previously reported to show changes in expression during dedifferentiation of human articular chondrocytes (HACs). Results Flow cytometry was used to identify 3 groups of surface antigens with differential expression patterns that were quite different from those previously reported on HACs. Two groups of antigens were expressed at high levels on human MSCs. The expression of the first group of antigens (CD44, CD58, CD81, CD90, CD105, and CD166) was decreased reversibly by the 3‐D alginate culture and irreversibly in the presence of TGFβ3, except for CD81, which showed reversible changes regardless of TGFβ3. The expression of the second group of antigens (CD49c, CD49e, and CD151) was decreased during chondrogenic differentiation only in the presence of TGFβ3. During all experimental stages, the expression of the third group of antigens (CD14, CD26, CD49f, CD54, CD106, CD119, and CD140a) was maintained at low levels (expressed on <30% of cells), although with some fluctuations. Conclusion We speculate that the second group of surface antigens could be negative markers for chondrogenic differentiation of human MSCs.
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