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Enhanced chondrogenesis in a coculture system with genetically manipulated dedifferentiated chondrocytes and ATDC5 cells
Author(s) -
Yao Yongchang,
Zhang Tingshuai,
Chen Hanzheng,
Zheng Shicong,
Chen Yi,
Zhang Shujiang
Publication year - 2020
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.27482
Subject(s) - chondrogenesis , transfection , microbiology and biotechnology , articular cartilage repair , cartilage , regeneration (biology) , viability assay , transforming growth factor , sox9 , tissue engineering , chondrocyte , biology , chemistry , cell culture , cell , articular cartilage , osteoarthritis , anatomy , gene , gene expression , medicine , pathology , biochemistry , genetics , alternative medicine
Articular cartilage repair after injury is a great challenge worldwide due to its nerveless and avascular features. Tissue engineering is proposed as a promising alternative for cartilage regeneration. In this study, an adenoviral vector carrying the transforming growth factor‐β3 (TGF‐β3) gene was constructed and introduced into dedifferentiated chondrocytes, which were then cocultured with ATDC5 cells in an alginate hydrogel system. The results showed that the experimental groups exhibited better cell viability and higher levels of cartilage‐related genes than the control groups. In this coculture system, the chondrogenic differentiation of ATDC5 cells was effectively induced by TGF‐β3 and other latent cytokines that were produced by the transfected chondrocytes. Thus, this method can avoid the degradation of exogenous TGF‐β3, and it can protect ATDC5 cells during virus transfection to maintain cell viability and chondrogenic differentiation capability. Taken together, this study provides fresh insights for applying this genetically manipulated coculture system to cartilage repair in the future.