The effect of growth/differentiation factor-5 (GDF-5) on genotype and phenotype in human adult mesenchymal stem cells

被引:13
|
作者
Koch, H
Jadlowiec, JA
Fu, FH
Nonn, J
Merk, HR
Hollinger, JO
Campbell, PG
机构
[1] Univ Greifswald, Klin Orthopad & Orthopad Chirurg, D-17487 Greifswald, Germany
[2] Carnegie Mellon Univ, Bone Tissue Engn Ctr, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Med Ctr, Dept Orthopaed Surg, Pittsburgh, PA USA
[5] CMU, Inst Complex Engn Syst, Pittsburgh, PA USA
来源
关键词
GDF-5; human mesenchymal stem cells; tendon and ligament injury; quantitative real-time PCR;
D O I
10.1055/s-2004-822612
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Aim: To evaluate the effects of GDF-5 on genotype and phenotype of human mesenchymal stem cells (hMSC). Hypothesis: GDF-5 leads to up-regulation of the Type I-collagen (Col) gene without altering bone marker genes or alkaline phosphatase activity. Methods: To test our hypothesis hMSC were treated with rmGDF-5. Using quantitative real-time PCR we analyzed mRNA for Col, Runx2 and Osterix (Osx). Furthermore, we analyzed alkaline phosphatase activity (ALP) as a phenotypical bone marker. ANOVA and post hoc statistical analyses were used to determine differences among treatments (p<0.05). Results: HMSC showed a biphasic response in both Col and Runx2 after rmGDF-5. Initial up-regulation was followed by a significant down-regulation below controls. Interestingly, the controls presented with changes for Col and Runx2 over time. There was no Osx expression in either treated hMSC or controls. No significant differences could be detected in ALP. Conclusion: Increased expression of Col and Runx2 might indicate differentiation towards both osteoblast and fibroblast lineage. However, no Osx expression and no change in ALP support the assumption that rmGDF-5 does not lead to an osteoblast phenotype in hMSC. Our in vitro studies confirm a possible therapeutic benefit of GDF-5 in the treatment of tendon and ligament injuries and tissue engineering approaches. Further research is necessary to prove its clinical value.
引用
收藏
页码:248 / 253
页数:6
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