首页> 外文期刊>Acta biomaterialia >In vitro differentiation of chondrogenic ATDC5 cells is enhanced by culturing on synthetic hydrogels with various charge densities.
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In vitro differentiation of chondrogenic ATDC5 cells is enhanced by culturing on synthetic hydrogels with various charge densities.

机译:通过在具有各种电荷密度的合成水凝胶上进行培养,可增强软骨生成ATDC5细胞的体外分化。

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We investigated the behavior of chondrogenic ATDC5 cells on synthetic polymer gels with various charge densities: negatively charged poly(2-acrylamido-2-methyl-1-propanesulfonic acid) (PAMPS) gel, neutral poly(dimethylacrylamide) (PDMAAm) gel, and copolymer gels of 2-acrylamido-2-methyl-1-propanesulfonic acid and dimethylacrylamide P(AMPS-co-DMAAm) with different compositions (molar fractions of AMPS, F=0.25, 0.5, 0.75). In insulin-free maintenance medium, the ATDC5 cells cultured on the highly negatively charged gels - PAMPS gel and the P(AMPS-co-DMAAm) copolymer gels (F=0.75) - spread and became confluent at day 7, and interestingly formed nodules at day 14, expressing type II collagen and proteoglycan. This result demonstrates that the highly negatively charged gels can induce chondrogenic differentiation of ATDC5 cells even in insulin-free maintenance medium, in which the ATDC5 cells cultured on the standard polystyrene dish cannot differentiate into chondrocytes. In insulin-supplemented differentiation medium, ATDC5 cells cultured on the PDMAAm gel made focal adhesions, rapidly aggregated and formed large nodules within 7 days, expressing significantly greater levels of type II collagen and proteoglycan than cells cultured on the polystyrene dish and the negatively charged gels. These results showed that the neutral gel accelerated chondrogenic differentiation of ATDC5 cells cultured in the differentiation medium. We suggest that the highly negatively charged PAMPS gel and the neutral PDMAAm gel are interesting biomaterials for cartilage tissue engineering as a scaffold with the potential to induce chondrogenic differentiation.
机译:我们研究了软骨生成ATDC5细胞在具有不同电荷密度的合成聚合物凝胶上的行为:带负电荷的聚(2-丙烯酰胺基-2-甲基-1-丙烷磺酸)(PAMPS)凝胶,中性聚(二甲基丙烯酰胺)(PDMAAm)凝胶和2-丙烯酸酰胺基-2-甲基-1-丙磺酸和二甲基丙烯酰胺P(AMPS-co-DMAAm)的共聚物凝胶具有不同的组成(AMPS的摩尔分数,F = 0.25、0.5、0.75)。在无胰岛素的维持培养基中,在高度带负电荷的凝胶-PAMPS凝胶和P(AMPS-co-DMAAm)共聚物凝胶(F = 0.75)-上培养的ATDC5细胞在第7天扩散并汇合,有趣地形成了结节在第14天,表达II型胶原蛋白和蛋白聚糖。该结果表明,即使在无胰岛素的维持培养基中,带高负电荷的凝胶也可以诱导ATDC5细胞的软骨形成分化,其中在标准聚苯乙烯培养皿上培养的ATDC5细胞不能分化为软骨细胞。在补充胰岛素的分化培养基中,在PDMAAm凝胶上培养的ATDC5细胞在7天内形成粘着斑,迅速聚集并形成大的结节,表达的II型胶原蛋白和蛋白聚糖水平明显高于在聚苯乙烯培养皿和带负电荷的凝胶上培养的细胞。这些结果表明,中性凝胶加速了在分化培养基中培养的ATDC5细胞的软骨形成分化。我们建议,带高负电荷的PAMPS凝胶和中性PDMAAm凝胶是用于软骨组织工程的有趣生物材料,可作为具有诱导软骨分化潜能的支架。

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