Chasing Chimeras - The elusive stable chondrogenic phenotype.
Cartilage tissue engineering
Chondrocytes
Clinical trials
In vitro microenvironment
In vivo models
Stem cells
Journal
Biomaterials
ISSN: 1878-5905
Titre abrégé: Biomaterials
Pays: Netherlands
ID NLM: 8100316
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
03
08
2018
revised:
02
11
2018
accepted:
09
11
2018
pubmed:
20
11
2018
medline:
19
3
2020
entrez:
20
11
2018
Statut:
ppublish
Résumé
The choice of the best-suited cell population for the regeneration of damaged or diseased cartilage depends on the effectiveness of culture conditions (e.g. media supplements, three-dimensional scaffolds, mechanical stimulation, oxygen tension, co-culture systems) to induce stable chondrogenic phenotype. Herein, advances and shortfalls in in vitro, preclinical and clinical setting of various in vitro microenvironment modulators on maintaining chondrocyte phenotype or directing stem cells towards chondrogenic lineage are critically discussed. Chondrocytes possess low isolation efficiency, limited proliferative potential and rapid phenotypic drift in culture. Mesenchymal stem cells are relatively readily available, possess high proliferation potential, exhibit great chondrogenic differentiation capacity, but they tend to acquire a hypertrophic phenotype when exposed to chondrogenic stimuli. Embryonic and induced pluripotent stem cells, despite their promising in vitro and preclinical data, are still under-investigated. Although a stable chondrogenic phenotype remains elusive, recent advances in in vitro microenvironment modulators are likely to develop clinically- and commercially-relevant therapies in the years to come.
Identifiants
pubmed: 30453216
pii: S0142-9612(18)30791-9
doi: 10.1016/j.biomaterials.2018.11.014
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
199-225Informations de copyright
Copyright © 2018 Elsevier Ltd. All rights reserved.