Downregulation of carbonic anhydrase IX promotes Col10a1 expression in chondrocytes

• Published in: PloS one Vol. 8; no. 2; p. e56984
• Main Authors: Maruyama, Toshifumi, Miyamoto, Yoichi, Yamamoto, Gou, Yamada, Atsushi, Yoshimura, Kentaro, Suzawa, Tetsuo, Takami, Masamichi, Akiyama, Tomohito, Hoshino, Marie, Iwasa, Fuminori, Ikumi, Noriharu, Tachikawa, Tetsuhiko, Mishima, Kenji, Baba, Kazuyoshi, Kamijo, Ryutaro
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 18.02.2013; Public Library of Science (PLoS)
• Subjects: Animals; Basic Helix-Loop-Helix Transcription Factors - genetics; Biochemistry; Biology; Bromination; Cancer; Carbon dioxide; Carbonic anhydrase; Carbonic Anhydrase IX; Carbonic anhydrases; Carbonic Anhydrases - metabolism; Cartilage; Cell adhesion & migration; Cell Enlargement; Cell Hypoxia; Cell Proliferation; Chondrocytes; Chondrocytes - metabolism; Chondrocytes - pathology; Chondrogenesis; Collagen; Collagen Type X - genetics; Collagen Type X - metabolism; Cyclic AMP; Cyclic AMP-Dependent Protein Kinases - metabolism; Dental schools; Dentistry; Differentiation; Down-regulation; Embryos; Enzyme Activation; Enzyme inhibitors; Gene expression; Gene Expression Regulation; Genes; Growth Plate - metabolism; Hypoxia; Inhibitors; Kinases; Localization; Mice; Models, Biological; Pathology; Phosphodiesterase; Phosphorylation; Protein kinase A; Proteins; RNA; RNA Interference; Signal Transduction; siRNA; Studies; Transcription; Transcription factors; Tumors; Japan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0056984

Carbonic anhydrase (CA) IX is a transmembrane isozyme of CAs that catalyzes reversible hydration of CO(2). While it is known that CA IX is distributed in human embryonic chondrocytes, its role in chondrocyte differentiation has not been reported. In the present study, we found that Car9 mRNA and CA IX were expressed in proliferating but not hypertrophic chondrocytes. Next, we examined the role of CA IX in the expression of marker genes of chondrocyte differentiation in vitro. Introduction of Car9 siRNA to mouse primary chondrocytes obtained from costal cartilage induced the mRNA expressions of Col10a1, the gene for type X collagen α-1 chain, and Epas1, the gene for hypoxia-responsible factor-2α (HIF-2α), both of which are known to be characteristically expressed in hypertrophic chondrocytes. On the other hand, forced expression of CA IX had no effect of the proliferation of chondrocytes or the transcription of Col10a1 and Epas1, while the transcription of Col2a1 and Acan were up-regulated. Although HIF-2α has been reported to be a potent activator of Col10a1 transcription, Epas1 siRNA did not suppress Car9 siRNA-induced increment in Col10a1 expression, indicating that down-regulation of CA IX induces the expression of Col10a1 in chondrocytes in a HIF-2α-independent manner. On the other hand, cellular cAMP content was lowered by Car9 siRNA. Furthermore, the expression of Col10a1 mRNA after Car9 silencing was augmented by an inhibitor of protein kinase A, and suppressed by an inhibitor for phosphodiesterase as well as a brominated analog of cAMP. While these results suggest a possible involvement of cAMP-dependent pathway, at least in part, in induction of Col10a1 expression by down-regulation of Car9, more detailed study is required to clarify the role of CA IX in regulation of Col10a1 expression in chondrocytes.