Junctional epithelium and hemidesmosomes: tape and rivets for solving the “percutaneous device dilemma” in dental and other permanent implants
Data de publicació
2022-12ISSN
2452-199X
Resum
The percutaneous device dilemma describes etiological factors, centered around the disrupted epithelial tissue surrounding non-remodelable devices, that contribute to rampant percutaneous device infection. Natural percutaneous organs, in particular their extracellular matrix mediating the “device”/epithelium interface, serve as exquisite examples to inspire longer lasting long-term percutaneous device design. For example, the tooth's imperviousness to infection is mediated by the epithelium directly surrounding it, the junctional epithelium (JE). The hallmark feature of JE is formation of hemidesmosomes, cell/matrix adhesive structures that attach surrounding oral gingiva to the tooth's enamel through a basement membrane. Here, the authors survey the multifaceted functions of the JE, emphasizing the role of the matrix, with a particular focus on hemidesmosomes and their five main components. The authors highlight the known (and unknown) effects dental implant – as a model percutaneous device – placement has on JE regeneration and synthesize this information for application to other percutaneous devices. The authors conclude with a summary of bioengineering strategies aimed at solving the percutaneous device dilemma and invigorating greater collaboration between clinicians, bioengineers, and matrix biologists.
Tipus de document
Article
Versió del document
Versió publicada
Llengua
Anglès
Matèries (CDU)
616.3 - Patologia de l'aparell digestiu. Odontologia
Paraules clau
Pàgines
21
Publicat per
Elsevier
Col·lecció
18
Publicat a
Bioactive Materials
Citació
Fischer, Nicholas G.; Aparicio, Conrado. Junctional epithelium and hemidesmosomes: tape and rivets for solving the “percutaneous device dilemma” in dental and other permanent implants. Bioactive Materials, 2022, 18, p. 178-198. Disponible en: <https://www.sciencedirect.com/science/article/pii/S2452199X22001359>. Fecha de acceso: 19 abr. 2023. DOI: 10.1016/j.bioactmat.2022.03.019
Nota
This work was supported by the NIH/NIDCR under awards R01DE026117 (CA), F30DE029105 (NGF), and T90DE0227232 (NGF). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. This work was supported by the Assistant Secretary of Defense for Health Affairs through the Peer Reviewed Orthopaedic Research Program (PRORP) under Applied Research Award No W81XWH-20-1-0563 (CA). The U.S. Army Medical Research Acquisition Activity, 839 Chandler Street, Fort Detrick MD 21702-5014 is the awarding and administering acquisition office. Opinions, interpretations, conclusions, and recommendations are those of the authors and are not necessarily endorsed by the Department of Defense. The work was also supported by a 3M Science and Technology Fellowship (NGF). The funding bodies had no role in study design, the collection, analysis and interpretation of data, in the writing of the report, and in the decision to submit the article for publication. CA acknowledges support from the Fundacio ´ Bosch Aymerich through a FBA-BIST-UIC fellowship. IBEC is a member of the CERCA Programme/Generalitat de Catalunya.
Enllaç al document relacionat
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Drets
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