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Chemokine Regulation in Temporomandibular Joint Disease: A Comprehensive Review

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2023 Feb 25
PMID 36833336
Authors
Affiliations
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Abstract

Temporomandibular joint disorders (TMDs) are conditions that affect the muscles of mastication and joints that connect the mandible to the base of the skull. Although TMJ disorders are associated with symptoms, the causes are not well proven. Chemokines play an important role in the pathogenesis of TMJ disease by promoting chemotaxis inflammatory cells to destroy the joint synovium, cartilage, subchondral bone, and other structures. Therefore, enhancing our understanding of chemokines is critical for developing appropriate treatment of TMJ. In this review, we discuss chemokines including MCP-1, MIP-1α, MIP-3a, RANTES, IL-8, SDF-1, and fractalkine that are known to be involved in TMJ diseases. In addition, we present novel findings that CCL2 is involved in β-catenin-mediated TMJ osteoarthritis (OA) and potential molecular targets for the development of effective therapies. The effects of common inflammatory factors, IL-1β and TNF-α, on chemotaxis are also described. In conclusion, this review aims to provide a theoretical basis for future chemokine-targeted therapies for TMJ OA.

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References
1.
Meder W, Wendland M, Busmann A, Kutzleb C, Spodsberg N, John H . Characterization of human circulating TIG2 as a ligand for the orphan receptor ChemR23. FEBS Lett. 2003; 555(3):495-9. DOI: 10.1016/s0014-5793(03)01312-7. View

2.
Valesan L, Da-Cas C, Reus J, Denardin A, Garanhani R, Bonotto D . Prevalence of temporomandibular joint disorders: a systematic review and meta-analysis. Clin Oral Investig. 2021; 25(2):441-453. DOI: 10.1007/s00784-020-03710-w. View

3.
Ellingsen T, Hornung N, Moller B, Poulsen J, Stengaard-Pedersen K . Differential effect of methotrexate on the increased CCR2 density on circulating CD4 T lymphocytes and monocytes in active chronic rheumatoid arthritis, with a down regulation only on monocytes in responders. Ann Rheum Dis. 2006; 66(2):151-7. PMC: 1798497. DOI: 10.1136/ard.2006.054056. View

4.
Rot A, Krieger M, Brunner T, Bischoff S, Schall T, Dahinden C . RANTES and macrophage inflammatory protein 1 alpha induce the migration and activation of normal human eosinophil granulocytes. J Exp Med. 1992; 176(6):1489-95. PMC: 2119467. DOI: 10.1084/jem.176.6.1489. View

5.
Sukedai M, Tominaga K, Habu M, Matsukawa A, Nishihara T, Fukuda J . Involvement of tumor necrosis factor-alpha and interleukin-8 in antigen-induced arthritis of the rabbit temporomandibular joint. J Oral Pathol Med. 2004; 33(2):102-10. DOI: 10.1111/j.1600-0714.2004.00008.x. View