Evaluation of Discoidin domain receptor 1 (DDR1) in junctional epithelial permeability and wound healing
Epithelium is the periodontal first line of defense against microbial attacks. Discoidin domain receptor 1 (DDR1) is a collagen receptor expressed at the epithelium. Mice not expressing the receptor (Ddr1<sup>-/-</sup> mice) develop defects consistent with periodontitis, including epithelium downgrowth and bone loss. In this study, we investigated periodontal epithelial permeability by applying a fluorescent dye in the mouth of Ddr1<sup>+/+</sup> and Ddr1<sup>-/-</sup> mice. Additionally, we used histological methods to reveal differences in the localization of gingival proteins between Ddr1<sup>+/+</sup> and Ddr1<sup>-/-</sup>. Finally, we investigated the role of DDR1 in wound healing in human sections and in a live animal model. No differences in junctional epithelium (JE) permeability were observed between Ddr1<sup>+/+</sup> and Ddr1<sup>-/-</sup> mice, as expressed by the comparable presence of dye in the periodontal tissues of both types of mice. There were no differences in the localization of E-cadherin or collagens IV, VIII, and XVII between Ddr1<sup>+/+</sup> and Ddr1<sup>-/-</sup>. In human gingiva, DDR1 was expressed at the epithelial front, migrating to cover palatal wounds. The animal wound healing study revealed higher healing of skin wounds in Ddr1<sup>-/-</sup> than Ddr1<sup>+/+</sup> mice at 5 dpw. In conclusion, this study has elucidated a role for DDR1 in epithelial cell migration during skin wound healing.
Authors
- Anuja Doshi
- Christina Zachariadou
- Brian Lee Foster (ORCID: https://orcid.org/0000-0003-3444-0576)
- Dimitris N. Tatakis (ORCID: https://orcid.org/0000-0001-6327-3610)
Institutions
- University of Jordan (JO)
- University of British Columbia (CA)
- The Ohio State University (US)
- Case Western Reserve University (US)
- University at Buffalo, State University of New York (US)
Publication Details
- Journal
- Journal of Periodontology
- Published
- 2025-12-02
- DOI
- https://doi.org/10.1002/jper.70031
- Citations
- 1
- Primary Topic
- Cell Adhesion Molecules Research
- Type
- article
- Field-Weighted Citation Impact
- 1.62