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Biomimetic cell-laden meha hydrogels for the regeneration of cartilage tissue

Authors :
Tsanaktsidou, Evgenia
Kammona, Olga
Labude, Norina
Neuss, Sabine
Krüger, Melanie
Kock, Linda
Kiparissides, Costas
Tsanaktsidou, Evgenia
Kammona, Olga
Labude, Norina
Neuss, Sabine
Krüger, Melanie
Kock, Linda
Kiparissides, Costas
Source :
Polymers vol.12 (2020) nr.7 [ISSN 2073-4360]
Publication Year :
2020

Abstract

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.

Details

Database :
OAIster
Journal :
Polymers vol.12 (2020) nr.7 [ISSN 2073-4360]
Notes :
Tsanaktsidou, Evgenia
Publication Type :
Electronic Resource
Accession number :
edsoai.on1260210787
Document Type :
Electronic Resource