Hegewald A A, Ringe J, Bartel J, Krüger I, Notter M, Barnewitz D, Kaps C, Sittinger M
Tissue Engineering Laboratory, Department of Rheumatology, Charité-University Medicine Berlin, Campus Mitte, Berlin, Germany.
Tissue Cell. 2004 Dec;36(6):431-8. doi: 10.1016/j.tice.2004.07.003.
Mesenchymal stem cells (MSC) have the potential to differentiate into distinct mesenchymal tissues including cartilage, which suggest these cells as an attractive cell source for cartilage tissue engineering approaches. Our objective was to study the effects of TGF-beta1, hyaluronic acid and synovial fluid on chondrogenic differentiation of equine MSC. For that, bone marrow was aspirated from the tibia of one 18-month-old horse (Haflinger) and MSC were isolated using percoll-density centrifugation. To promote chondrogenesis, MSC were centrifuged to form a micromass and were cultured in a medium containing 10 ng/ml TGF-beta1 or 0.1mg/ml hyaluronic acid (Hylartil, Ostenil) or either 5%, 10% or 50% autologous synovial fluid as the chondrogenesis inducing factor. Differentiation along the chondrogenic lineage was documented by type II collagen and proteoglycan expression. MSC induced by TGF-beta1 alone showed the highest proteoglycan expression. Combining TGF-beta1 with hyaluronic acid could not increase the proteoglycan expression. Cultures stimulated by autologous synovial fluid (independent of concentration) and hyaluronic acid demonstrated a pronounced, but lower proteoglycan expression than cultures stimulated by TGF-beta1. The expression of cartilage-specific type II collagen was high and about the same in all stimulated cultures. In summary, hyaluronic acid and autologous synovial fluid induces chondrogenesis of equine mesenchymal stem cells, which encourage tissue engineering applications of MSC in chondral defects, as the natural environment in the joint is favorable for chondrogenic differentiation.
间充质干细胞(MSC)有分化为包括软骨在内的不同间充质组织的潜力,这表明这些细胞是软骨组织工程方法中一种有吸引力的细胞来源。我们的目的是研究转化生长因子β1(TGF-β1)、透明质酸和滑液对马MSC软骨形成分化的影响。为此,从一匹18个月大的马(哈芬兰马)的胫骨中抽取骨髓,使用 Percoll 密度离心法分离 MSC。为促进软骨形成,将 MSC 离心形成微团,并在含有10 ng/ml TGF-β1 或 0.1mg/ml 透明质酸(Hylartil, Ostenil)或 5%、10% 或 50% 自体滑液作为软骨形成诱导因子的培养基中培养。通过 II 型胶原蛋白和蛋白聚糖的表达记录软骨形成谱系的分化情况。单独由 TGF-β1 诱导的 MSC 显示出最高的蛋白聚糖表达。将 TGF-β1 与透明质酸结合并不能增加蛋白聚糖的表达。由自体滑液(与浓度无关)和透明质酸刺激的培养物显示出明显的蛋白聚糖表达,但低于由 TGF-β1 刺激的培养物。在所有受刺激的培养物中,软骨特异性 II 型胶原蛋白的表达都很高且大致相同。总之,透明质酸和自体滑液可诱导马间充质干细胞的软骨形成,这鼓励了 MSC 在软骨缺损中的组织工程应用,因为关节中的自然环境有利于软骨形成分化。