Abstract
AbstractThe potential therapeutic role of the Dental Pulp Stem Cells Secretome (SECR) in a rat model of experimentally induced Temporomandibular Joint (TMJ) Osteoarthritis (OA) was evaluated. Proteomic profiling of the human SECR under specific oxygen tension (5% O2) and stimulation with Tumor Necrosis Factor-alpha (TNF-α) was performed. SECR and respective cell lysates (CL) samples were collected and subjected to SDS-PAGE, followed by LC-MS/MS analysis. The identified proteins were analyzed with Bioinformatic tools. The anti-inflammatory properties of SECR were assessed via an in vitro murine macrophages model, and were further validated in vivo, in a rat model of chemically-induced TMJ-OA by weekly recording of the head withdrawal threshold, the food intake, and the weight change, and radiographically and histologically at 4- and 8-weeks post-treatment. SECR analysis revealed the presence of 50 proteins that were enriched and/or statistically significantly upregulated compared to CL, while many of those proteins were involved in pathways related to “extracellular matrix organization” and “immune system”. SECR application in vitro led to a significant downregulation on the expression of pro-inflammatory genes (MMP-13, MMP-9, MMP-3 and MCP-1), while maintaining an increased expression of IL-10 and IL-6. SECR application in vivo had a significant positive effect on all the clinical parameters, resulting in improved food intake, weight, and pain suppression. Radiographically, SECR application had a significant positive effect on trabecular bone thickness and bone density compared to the saline-treated group. Histological analysis indicated that SECR administration reduced inflammation, enhanced ECM and subchondral bone repair and regeneration, thus alleviating TMJ degeneration.
Graphical Abstract
Funder
Aristotle University of Thessaloniki
Publisher
Springer Science and Business Media LLC
Reference61 articles.
1. Wang, X. D., Zhang, J. N., Gan, Y. H., & Zhou, Y. H. (2015). Current understanding of pathogenesis and treatment of TMJ osteoarthritis. Journal of Dental Research, 94, 666–673. https://doi.org/10.1177/0022034515574770
2. Zarb, G. A., & Carlsson, G. E. (1999). Temporomandibular disorders: osteoarthritis. Journal of Orofacial Pain, 13, 295–306.
3. Tanaka, E., Detamore, M. S., & Mercuri, L. G. (2008). Degenerative disorders of the Temporomandibular joint: etiology, diagnosis, and treatment. Journal of Dental Research, 87, 296–307. https://doi.org/10.1177/154405910808700406
4. Eming, S. A., Wynn, T. A., & Martin, P. (2017). Inflammation and metabolism in tissue repair and regeneration. Science, 1979, 356.
5. Prigogine, I., & Nicolis, G. (1967). On symmetry-breaking instabilities in dissipative systems. The Journal of Chemical Physics, 46. https://doi.org/10.1063/1.1841255
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