Photobiomodulation of inflammatory-cytokine-related effects in a 3-D culture model with gingival fibroblasts

dc.contributor.authorCardoso, Laís Medeiros [UNESP]
dc.contributor.authorPansani, Taisa Nogueira [UNESP]
dc.contributor.authorHebling, Josimeri [UNESP]
dc.contributor.authorde Souza Costa, Carlos Alberto [UNESP]
dc.contributor.authorBasso, Fernanda Gonçalves
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUNAERP
dc.date.accessioned2020-12-12T01:55:45Z
dc.date.available2020-12-12T01:55:45Z
dc.date.issued2020-07-01
dc.description.abstractThe aim of this study was to assess the effects of IL-6 and IL-8 cytokines on human gingival fibroblasts (HGF) cultured in a 3-D model and the possible photobiomodulation (PBM) of such effects by low-level laser therapy. In complete culture medium (DMEM), HGF from a healthy patient were seeded in a type I collagen matrix inserted into 24-well plates. After 5 days of incubation, the cytokines were added or not to serum-free DMEM, which was applied to the cell-enriched matrices. Then, PBM was performed: three consecutive irradiations using LaserTable diode device (780 nm, 0.025 W) at 0.5 J/cm2 were delivered or not to the cells. Twenty-four hours after the last irradiation, cell viability and morphology, gene expression, and synthesis of inflammatory cytokines and growth factors were assessed. The histological evaluation demonstrated that, for all groups, matrices presented homogeneous distribution of cells with elongated morphology. However, numerous cytokine-exposed cells were rounded. IL-6 and IL-8 decreased cell viability, synthesis of VEGF, and gene expression of collagen type I. PBM enhanced cell density in the matrices and stimulated VEGF expression, even after IL-6 challenge. Reduced TNF-α synthesis occurred in those cells subjected to PBM. In conclusion, PBM can penetrate collagen matrix and stimulate HGF, highlighting the relevance of this research model for further phototherapy studies and in vitro biomodulation of the healing process.en
dc.description.affiliationDepartment of Physiology and Pathology Araraquara School of Dentistry UNESP, R. Humaita, 1680
dc.description.affiliationDepartment of Pediatric Dentistry Araraquara School of Dentistry UNESP
dc.description.affiliationDepartment of Dentistry Universidade de Ribeirão Preto UNAERP
dc.description.affiliationUnespDepartment of Physiology and Pathology Araraquara School of Dentistry UNESP, R. Humaita, 1680
dc.description.affiliationUnespDepartment of Pediatric Dentistry Araraquara School of Dentistry UNESP
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent1205-1212
dc.identifierhttp://dx.doi.org/10.1007/s10103-020-02974-8
dc.identifier.citationLasers in Medical Science, v. 35, n. 5, p. 1205-1212, 2020.
dc.identifier.doi10.1007/s10103-020-02974-8
dc.identifier.issn1435-604X
dc.identifier.issn0268-8921
dc.identifier.scopus2-s2.0-85078974533
dc.identifier.urihttp://hdl.handle.net/11449/200031
dc.language.isoeng
dc.relation.ispartofLasers in Medical Science
dc.sourceScopus
dc.subject3-D cell culture
dc.subjectCytokines
dc.subjectGingival fibroblasts
dc.subjectLow-level laser therapy
dc.titlePhotobiomodulation of inflammatory-cytokine-related effects in a 3-D culture model with gingival fibroblastsen
dc.typeArtigo
unesp.author.lattes4517484241515548[4]
unesp.author.orcid0000-0002-7170-2371[5]
unesp.author.orcid0000-0002-7455-6867[4]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Odontologia, Araraquarapt
unesp.departmentClínica Infantil - FOARpt
unesp.departmentFisiologia e Patologia - FOARpt

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