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

  • Evgenia Tsanaktsidou
  • , Olga Kammona
  • , Norina Labude
  • , Sabine Neuss
  • , Melanie Krüger
  • , Linda Kock
  • , Costas Kiparissides (Corresponding author)

Onderzoeksoutput: Bijdrage aan tijdschriftTijdschriftartikelAcademicpeer review

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Samenvatting

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.

Originele taal-2Engels
Artikelnummer1598
Aantal pagina's19
TijdschriftPolymers
Volume12
Nummer van het tijdschrift7
DOI's
StatusGepubliceerd - jul. 2020

Bibliografische nota

Funding Information:
Funding: The present research has received funding from the EU Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement No 642687.

Publisher Copyright:
© 2020 by the authors.

Financiering

Funding: The present research has received funding from the EU Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement No 642687.

FinanciersFinanciernummer
European Union’s Horizon Europe research and innovation programme
European Union’s Horizon Europe research and innovation programme
H2020 Marie Skłodowska-Curie Actions642687

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