Down-regulation of transglutaminase 2 stimulates redifferentiation of dedifferentiated chondrocytes through enhancing glucose metabolism

Kyoung Won Ko, Bogyu Choi, Sunghyun Park, Yoshie Arai, Won Chul Choi, Joong Myung Lee, Hojae Bae, In Bo Han, Soo Hong Lee

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Expansion of chondrocytes for repair of articular cartilage can lead to dedifferentiation, making it difficult to obtain a sufficient quantity of chondrocytes. Although previous studies have suggested that culture in a three-dimensional environment induces redifferentiation of dedifferentiated chondrocytes, its underlying mechanisms are still poorly understood in terms of metabolism compared with a two-dimensional environment. In this study, we demonstrate that attenuation of transglutaminase 2 (TG2), a multifunctional enzyme, stimulates redifferentiation of dedifferentiated chondrocytes. Fibroblast-like morphological changes increased as TG2 expression increased in passage-dependent manner. When dedifferentiated chondrocytes were cultured in a pellet culture system, TG2 expression was reduced and glycolytic enzyme expression up-regulated. Previous studies demonstrated that TG2 influences energy metabolism, and impaired glycolytic metabolism causes chondrocyte dedifferentiation. Interestingly, TG2 knockdown improved chondrogenic gene expression, glycolytic enzyme expression, and lactate production in a monolayer culture system. Taken together, down-regulation of TG2 is involved in redifferentiaton of dedifferentiated chondrocytes through enhancing glucose metabolism.

Original languageEnglish
Article number2359
JournalInternational Journal of Molecular Sciences
Volume18
Issue number11
DOIs
StatePublished - 7 Nov 2017

Keywords

  • Chondrocytes
  • Glycolytic metabolism
  • Redifferentiation
  • Transglutaminase 2

Fingerprint

Dive into the research topics of 'Down-regulation of transglutaminase 2 stimulates redifferentiation of dedifferentiated chondrocytes through enhancing glucose metabolism'. Together they form a unique fingerprint.

Cite this