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ID 65938
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Kato, Soma Department of Biochemistry and Molecular Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kawata, Kazumi Department of Biochemistry and Molecular Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID researchmap
Nishida, Takashi Department of Biochemistry and Molecular Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons researchmap
Mizukawa, Tomomi Department of Biochemistry and Molecular Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Takigawa, Masaharu Advanced Research Center for Oral and Craniofacial Sciences, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons researchmap
Iida, Seiji Department of Oral Maxillofacial Reconstructive Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons researchmap
Kubota, Satoshi Department of Biochemistry and Molecular Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons researchmap
Abstract
Cellular communication network factor 2 (CCN2) molecules promote endochondral ossification and articular cartilage regeneration, and circular RNAs (circRNAs), which arise from various genes and regulate gene expression by adsorbing miRNAs, are known to be synthesized from CCN2 in human vascular endothelial cells and other types of cells. However, in chondrocytes, not only the function but also the presence of CCN2-derived circRNA remains completely unknown. In the present study, we investigated the expression and function of CCN2-derived circRNAs in chondrocytes. Amplicons smaller than those from known CCN2-derived circRNAs were observed using RT-PCR analysis that could specifically amplify CCN2-derived circRNAs in human chondrocytic HCS-2/8 cells. The nucleotide sequences of the PCR products indicated novel circRNAs in the HCS-2/8 cells that were different from known CCN2-derived circRNAs. Moreover, the expression of several Ccn2-derived circRNAs in murine chondroblastic ATDC5 cells was confirmed and observed to change alongside chondrocytic differentiation. Next, one of these circRNAs was knocked down in HCS-2/8 cells to investigate the function of the human CCN2-derived circRNA. As a result, CCN2-derived circRNA knockdown significantly reduced the expression of aggrecan mRNA and proteoglycan synthesis. Our data suggest that CCN2-derived circRNAs are expressed in chondrocytes and play a role in chondrogenic differentiation.
Keywords
Chondrocyte
CCN2
Circular RNA
ACAN
Chondrocytic differentiation
Note
The version of record of this article, first published in Journal of Cell Communication and Signaling, is available online at Publisher’s website: http://dx.doi.org/10.1007/s12079-023-00782-7
Published Date
2023-09-11
Publication Title
Journal of Cell Communication and Signaling
Volume
volume17
Issue
issue4
Publisher
Springer Science and Business Media LLC
Start Page
1501
End Page
1515
ISSN
1873-9601
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Author(s) 2023
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isVersionOf https://doi.org/10.1007/s12079-023-00782-7
License
http://creativecommons.org/licenses/by/4.0/
Citation
Kato, S., Kawata, K., Nishida, T. et al. Expression and function of CCN2-derived circRNAs in chondrocytes. J. Cell Commun. Signal. 17, 1501–1515 (2023). https://doi.org/10.1007/s12079-023-00782-7
Funder Name
Japan Society for the Promotion of Science
助成番号
JP19K10109
JP19H03817
JP20K09889
JP20K20611
JP21H03105
JP23K17439