An organotypic oral mucosal infection model to study host-pathogen interactions
dc.contributor.author | Gould, SJ | |
dc.contributor.author | Foey, AD | |
dc.contributor.author | Salih, VM | |
dc.date.accessioned | 2023-11-01T15:04:15Z | |
dc.date.available | 2023-11-01T15:04:15Z | |
dc.date.issued | 2023-01 | |
dc.identifier.issn | 2041-7314 | |
dc.identifier.issn | 2041-7314 | |
dc.identifier.other | ARTN 20417314231197310 | |
dc.identifier.uri | https://pearl.plymouth.ac.uk/handle/10026.1/21504 | |
dc.description.abstract |
Early in vitro oral mucosal infection models (OMMs) failed to consider the suitability of the model environment to represent the host immune response. Denture stomatitis (DS) is mediated by Candida albicans, but the role of Staphylococcus aureus remains uncertain. A collagen hydrogel-based OMM containing HaCaT and HGF cell types was developed, characterised and employed to study of tissue invasion and pro-inflammatory cytokine production in response to pathogens. Models formed a robust epithelium. Despite their inflammatory baseline, 24-h infection with C. albicans, and/or S. aureus led to tissue invasion, and significantly upregulated IL-6 and IL-8 production by OMMs when compared to the unstimulated control. No significant difference in IL-6 or IL-8 production by OMMs was observed between single and dual infections. These attributes indicate that this newly developed OMM is suitable for the study of DS and could be implemented for the wider study of oral infection. | |
dc.format.extent | 20417314231197310- | |
dc.format.medium | Electronic-eCollection | |
dc.language | en | |
dc.publisher | SAGE Publications | |
dc.subject | Candida albicans | |
dc.subject | Staphylococcus aureus | |
dc.subject | organotypic | |
dc.subject | oral mucosa | |
dc.subject | infection model | |
dc.subject | tissue-engineering | |
dc.subject | denture stomatitis | |
dc.title | An organotypic oral mucosal infection model to study host-pathogen interactions | |
dc.type | journal-article | |
dc.type | Article | |
plymouth.author-url | https://www.ncbi.nlm.nih.gov/pubmed/37873034 | |
plymouth.volume | 14 | |
plymouth.publisher-url | http://dx.doi.org/10.1177/20417314231197310 | |
plymouth.publication-status | Published | |
plymouth.journal | Journal of Tissue Engineering | |
dc.identifier.doi | 10.1177/20417314231197310 | |
plymouth.organisational-group | |Plymouth | |
plymouth.organisational-group | |Plymouth|Research Groups | |
plymouth.organisational-group | |Plymouth|Faculty of Health | |
plymouth.organisational-group | |Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED) | |
plymouth.organisational-group | |Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED)|CBR | |
plymouth.organisational-group | |Plymouth|REF 2021 Researchers by UoA | |
plymouth.organisational-group | |Plymouth|Users by role | |
plymouth.organisational-group | |Plymouth|Users by role|Academics | |
plymouth.organisational-group | |Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine | |
plymouth.organisational-group | |Plymouth|REF 2021 Researchers by UoA|UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy | |
plymouth.organisational-group | |Plymouth|Faculty of Health|Peninsula Dental School | |
plymouth.organisational-group | |Plymouth|Faculty of Health|School of Biomedical Sciences | |
plymouth.organisational-group | |Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine|UoA01 Clinical Medicine | |
dc.publisher.place | England | |
dcterms.dateAccepted | 2023-08-10 | |
dc.date.updated | 2023-11-01T15:04:08Z | |
dc.rights.embargodate | 2023-11-2 | |
dc.identifier.eissn | 2041-7314 | |
rioxxterms.versionofrecord | 10.1177/20417314231197310 |