Papers

Peer-reviewed
Oct, 2011

Novel effects of CCN3 that may direct the differentiation of chondrocytes

FEBS LETTERS
  • Danilo Janune
  • ,
  • Satoshi Kubota
  • ,
  • Takashi Nishida
  • ,
  • Harumi Kawaki
  • ,
  • Bernard Perbal
  • ,
  • Seiji Iida
  • ,
  • Masaharu Takigawa

Volume
585
Number
19
First page
3033
Last page
3040
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1016/j.febslet.2011.08.024
Publisher
ELSEVIER SCIENCE BV

Identification and characterization of local molecules directing the differentiation of chondrocytes to either transient or permanent cartilage are major issues in cartilage biology. Here, we found CCN family protein 3 (CCN3) was abundantly produced in rat developing epiphyseal cartilage. Evaluations in vitro showed that CCN3 repressed epiphyseal chondrocyte proliferation, while promoting matrix production in multiple assays performed. Furthermore, CCN3 enhanced the articular chondrocytic phenotype; whereas it repressed the one representing endochondral ossification. Additionally, the phenotype of growth plate chondrocytes and chondrogenic progenitors also appeared to be affected by CCN3 in a similar manner. These findings suggest a significant role of CCN3 in inducing chondrocytes to articular ones during joint formation. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Link information
DOI
https://doi.org/10.1016/j.febslet.2011.08.024
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/21871891
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000295473600017&DestApp=WOS_CPL
ID information
  • DOI : 10.1016/j.febslet.2011.08.024
  • ISSN : 0014-5793
  • Pubmed ID : 21871891
  • Web of Science ID : WOS:000295473600017

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