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Retinoic acid inhibits chondrogenesis of mesenchymal cells by sustaining expression of N‐cadherin and its associated proteins
Author(s) -
Cho SeoHyun,
Oh ChunDo,
Kim SongJa,
Kim IlChul,
Chun JangSoo
Publication year - 2003
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.10553
Subject(s) - chondrogenesis , microbiology and biotechnology , retinoic acid , chondrocyte , mesenchymal stem cell , chemistry , cytochalasin d , cadherin , cartilage , cellular differentiation , downregulation and upregulation , cytoskeleton , cell , biology , biochemistry , in vitro , anatomy , gene
Retinoic acid (RA) is a well‐known regulator of chondrocyte phenotype. RA inhibits chondrogenic differentiation of mesenchymal cells and also causes loss of differentiated chondrocyte phenotype. The present study investigated the mechanisms underlying RA regulation of chondrogenesis. RA treatment in chondrifying mesenchymal cells did not affect precartilage condensation, but blocked progression from precartilage condensation to cartilage nodule formation. This inhibitory effect of RA was independent of protein kinase C and extracellular signal‐regulated protein kinase, which are positive and negative regulators of cartilage nodule formation, respectively. The progression from precartilage condensation to cartilage nodule requires downregulation of N‐cadherin expression. However, RA treatment caused sustained expression of N‐cadherin and its associated proteins including α‐ and β‐catenin suggesting that modulation of expression of these molecules is associated with RA‐induced inhibition of chondrogenesis. This hypothesis was supported by the observation that disruption of the actin cytoskeleton by cytochalasin D (CD) blocks RA‐induced sustained expression of cell adhesion molecules and overcomes RA‐induced inhibition of chondrogenesis. Taken together, our results suggest RA inhibits chondrogenesis by stabilizing cell‐to‐cell interactions at the post‐precartilage condensation stage. J. Cell. Biochem. 89: 837–847, 2003. © 2003 Wiley‐Liss, Inc.