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Fabrication of stem cell heterospheroids with sustained-release chitosan and poly(lactic-co-glycolic acid) microspheres to guide cell fate toward chondrogenic differentiation

Authors
Nguyen, Tiep TienKil, Yun-SeoSung, Jong-HyukYoun, Yu SeokJeong, Ji HoonLee, Jung HeonJiang, Hu-LinYook, SimmyungNam, Joo-WonJeong, Jee-Heon
Issue Date
Apr-2024
Publisher
Elsevier B.V.
Keywords
Chondrogenesis; Heterospheroid; Stem cell
Citation
International Journal of Biological Macromolecules, v.263
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Biological Macromolecules
Volume
263
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/110516
DOI
10.1016/j.ijbiomac.2024.130356
ISSN
0141-8130
1879-0003
Abstract
Mesenchymal stem cell (MSC)-based therapies show great potential in treating various diseases. However, control of the fate of injected cells needs to be improved. In this work, we developed an efficient methodology for modulating chondrogenic differentiation of MSCs. We fabricated heterospheroids with two sustained-release depots, a quaternized chitosan microsphere (QCS-MP) and a poly (lactic-co-glycolic acid) microsphere (PLGA-MP). The results show that heterospheroids composed of 1 × 104 to 5 × 104 MSCs formed rapidly during incubation in methylcellulose medium and maintained high cell viability in long-term culture. The MPs were uniformly distributed in the heterospheroids, as shown by confocal laser scanning microscopy. Incorporation of transforming growth factor beta 3 into QCS-MPs and of dexamethasone into PLGA-MPs significantly promoted the expression of chondrogenic genes and high accumulation of glycosaminoglycan in heterospheroids. Changes in crucial metabolites in the dual drug depot–engineered heterospheroids were also evaluated using 1H NMR-based metabolomics analysis to verify their successful chondrogenic differentiation. Our heterospheroid fabrication platform could be used in tissue engineering to study the effects of various therapeutic agents on stem cell fate. © 2024
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