Abstract
Osteoarthritis represents a chronic degenerative joint disease with exceptional clinical relevance.Polymorphisms of the CALCA gene, giving rise to either a procalcitonin/calcitonin (PCT/CT) or acalcitonin gene-related peptide alpha (αCGRP) transcript by alternative splicing, were reported to beassociated with the development of osteoarthritis. The objective of this study was to investigate therole of both PCT/CT and αCGRP transcripts in a mouse model of post-traumatic osteoarthritis (ptOA).WT, αCGRP−/− and CALCA−/− mice were subjected to anterior cruciate ligament transection (ACLT) toinduce ptOA of the knee. Mice were sacrificed 4 and 8 weeks post-surgery, followed by micro-CT andhistological evaluation. Here we show that the expression of both PCT/CT and αCGRP transcripts isinduced in ptOA knees. CALCA−/− mice show increased cartilage degeneration and subchondral boneloss with elevated osteoclast numbers compared to αCGRP−/− and WT mice. Osteophyte formation isreduced to the same extent in CALCA−/− and αCGRP−/− mice compared to WT controls, while areduced synovitis score is noticed exclusively in mice lacking CALCA. Our data show that expressionof the PCT/CT transcript protects from the progression of ptOA, while αCGRP promotes osteophyteformation, suggesting that CALCA-encoded peptides may represent novel targets for the treatmentof ptOA.
Originalsprog | Engelsk |
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Artikelnummer | 223 |
Tidsskrift | Communications Biology |
Vol/bind | 7 |
Udgave nummer | 1 |
Antal sider | 12 |
ISSN | 2399-3642 |
DOI | |
Status | Udgivet - 2024 |
Bibliografisk note
Funding Information:S.J. is funded by the China Scholarship Council. T.M. is participant in the BIH Charité Clinician Scientist Program funded by the Charité—Universitätsmedizin Berlin, and the Berlin Institute of Health at Charité (BIH).
Publisher Copyright:
© The Author(s) 2024.