Progenitor cells from cartilageNo osteoarthritis-grade-specific differences in stem cell marker expression

被引:23
作者
Bernstein, Peter [1 ]
Sperling, Ines [1 ]
Corbeil, Denis [2 ]
Hempel, Ute [3 ]
Fickert, Stefan [4 ,5 ]
机构
[1] Univ Hosp Carl Gustav Carus, Dept Orthopaed, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Tissue Engn Labs, D-01307 Dresden, Germany
[3] Tech Univ Dresden, Inst Physiol Chem, D-01307 Dresden, Germany
[4] Sporthopaedicum Straubing Regensburg, D-94315 Straubing, Germany
[5] Heidelberg Univ, Med Fac Mannheim, D-68167 Mannheim, Germany
关键词
chondrogenic progenitors; dedifferentiation; mesenchymal stromal cell; osteoarthritis; surface markers; SULFATED GLYCOSAMINOGLYCANS; CHONDROCYTES; DIFFERENTIATION; CULTURES; BIOLOGY;
D O I
10.1002/btpr.1668
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Tissue engineering efforts for the fabrication of cartilage substitutes head toward applicability in osteoarthritis (OA). Progenitor cells can be harvested from the osteoarthritic joint itself, resembling multipotent mesenchymal stromal cells (MSC). Our objective was to analyze MSC characteristics of those cells in respect to the OA-related damage of their harvest site. OA cartilage was obtained from six patients during alloarthroplastic knee surgery, sample grading was done according to Outerbridge's classification. Upon enzymatic dissociation, primary chondrocytes were expanded in two-dimensional monolayer culture. At distinct cell passages, the process of dedifferentiation was phenotypically monitored; cell surface expression of classical MSC markers was analyzed by flow cytometry. Cells were subjected to chondrogenesis and osteogenesis after their fourth passage. At third passage, 95% of cells became positive for cluster of differentiation (CD)105 and further subclassification revealed that the majority of them were positive for both CD73 and CD90. CD105+CD73+CD90+ phenotype meets thus the minimal surface antigen criteria for MSC definition. More than one-third of dedifferentiated chondrocytes displayed a coexpression of CD9+CD166+CD90+ and to a lesser extent CD105+CD73+CD44+, irrespective of the stage of the original cartilage degradation. Finally, we could successfully demonstrate a redifferentiation of these progenitors into sulfated glycosaminoglycan producing cells. The basic level of alkaline phosphatase activity could not be enhanced upon osteogenic differentiation. In conclusion, chondrogenic progenitors derived from OA cartilages with low or high Outerbridge's grade can be seen as a potential cellular source for cartilage replacement. (c) 2012 American Institute of Chemical Engineers Biotechnol. Prog.29;206-212, 2013
引用
收藏
页码:206 / 212
页数:7
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