| Literature DB >> 32985318 |
X Yuan1, J Chen1,2, J A Grauer1,3, Q Xu1,4, L A Van Brunt1, J A Helms1.
Abstract
The most fundamental function of an epithelial tissue is to act as a barrier, regulating interactions between the external environment and the body. This barrier function typically requires a contiguous cell layer but since teeth penetrate the oral epithelium, a modified barrier has evolved, called the junctional epithelium (JE). In health, the JE attaches to the tooth, sealing the inside of the body against oral micro-organisms. Breakdown of the JE barrier results in periodontal ligament (PDL) disintegration, alveolar bone resorption, and ultimately tooth loss. Using lineage tracing and DNA pulse-chase analyses, we identified an anatomical location in the JE that supported both fast- and slow-cycling Wnt-responsive stem cells that contributed to self-renewal of the tissue. Stem cells produced daughter cells with an extraordinarily high rate of turnover that maintained JE integrity for 1.4 y in mice. Blocking cell proliferation via a chemotherapeutic agent 5-fluorouracil (5-Fu) eliminated fast-cycling stem cells, which caused JE degeneration, PDL destruction, and bone resorption. Upon removal of 5-Fu, slow-cycling stem cells regenerated both the structure and barrier function of the JE. Taken together, our studies identified a stem cell population in the JE and have potential clinical implications for prevention and treatment of periodontitis.Entities:
Keywords: Wnt signaling pathway; cell proliferation; epithelial cells; gingiva; periodontitis; stem cell research
Mesh:
Year: 2020 PMID: 32985318 PMCID: PMC8173348 DOI: 10.1177/0022034520960125
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116