Tsanaktsidou Evgenia, Kammona Olga, Labude Norina, Neuss Sabine, Krüger Melanie, Kock Linda, Kiparissides Costas
Department of Chemical Engineering, Aristotle University of Thessaloniki, P.O. Box 472, 54124 Thessaloniki, Greece.
Chemical Process & Energy Resources Institute, Centre for Research and Technology Hellas, P.O. Box 60361, 57001 Thessaloniki, Greece.
Polymers (Basel). 2020 Jul 18;12(7):1598. doi: 10.3390/polym12071598.
Methacrylated hyaluronic acid (MeHA) and chondroitin sulfate (CS)-biofunctionalized MeHA (CS-MeHA), were crosslinked in the presence of a matrix metalloproteinase 7 (MMP7)-sensitive peptide. The synthesized hydrogels were embedded with either human mesenchymal stem cells (hMSCs) or chondrocytes, at low concentrations, and subsequently cultured in a stem cell medium (SCM) or chondrogenic induction medium (CiM). The pivotal role of the synthesized hydrogels in promoting the expression of cartilage-related genes and the formation of neocartilage tissue despite the low concentration of encapsulated cells was assessed. It was found that hMSC-laden MeHA hydrogels cultured in an expansion medium exhibited a significant increase in the expression of chondrogenic markers compared to hMSCs cultured on a tissue culture polystyrene plate (TCPS). This favorable outcome was further enhanced for hMSC-laden CS-MeHA hydrogels, indicating the positive effect of the glycosaminoglycan binding peptide on the differentiation of hMSCs towards a chondrogenic phenotype. However, it was shown that an induction medium is necessary to achieve full span chondrogenesis. Finally, the histological analysis of chondrocyte-laden MeHA hydrogels cultured on an ex vivo osteochondral platform revealed the deposition of glycosaminoglycans (GAGs) and the arrangement of chondrocyte clusters in isogenous groups, which is characteristic of hyaline cartilage morphology.
甲基丙烯酸化透明质酸(MeHA)和硫酸软骨素(CS)生物功能化的MeHA(CS-MeHA)在基质金属蛋白酶7(MMP7)敏感肽存在的情况下进行交联。合成的水凝胶以低浓度包埋人骨髓间充质干细胞(hMSCs)或软骨细胞,随后在干细胞培养基(SCM)或软骨诱导培养基(CiM)中培养。评估了合成水凝胶在促进软骨相关基因表达和新软骨组织形成方面的关键作用,尽管包封细胞浓度较低。结果发现,与在组织培养聚苯乙烯板(TCPS)上培养的hMSCs相比,在扩增培养基中培养的负载hMSC的MeHA水凝胶中软骨生成标志物的表达显著增加。对于负载hMSC的CS-MeHA水凝胶,这一良好结果进一步增强,表明糖胺聚糖结合肽对hMSCs向软骨生成表型分化具有积极作用。然而,研究表明,需要诱导培养基才能实现完全的软骨生成。最后,对在体外骨软骨平台上培养的负载软骨细胞的MeHA水凝胶进行组织学分析,结果显示有糖胺聚糖(GAGs)沉积以及软骨细胞簇在同源组中的排列,这是透明软骨形态的特征。