Blocking of Caspases Exerts Anti-Inflammatory Effects on Periodontal Cells

dc.contributor.authorPanahipour, Layla
dc.contributor.authorCervantes, Lara Cristina Cunha [UNESP]
dc.contributor.authorAbbasabadi, Azarakhsh Oladzad
dc.contributor.authorSordi, Mariane Beatriz
dc.contributor.authorKargarpour, Zahra
dc.contributor.authorGruber, Reinhard
dc.contributor.institutionMedical University of Vienna
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Federal de Santa Catarina (UFSC)
dc.contributor.institutionUniversity of Bern
dc.contributor.institutionAustrian Cluster for Tissue Regeneration
dc.date.accessioned2023-03-01T20:27:42Z
dc.date.available2023-03-01T20:27:42Z
dc.date.issued2022-07-01
dc.description.abstractPeriodontitis is an inflammatory process that is associated with caspase activity. Caspases could thus become molecular targets for the modulation of the inflammatory response to harmful factors, such as lipopolysaccharides (LPS) and TNFα. Here, the impact of the pan-caspase inhibitor Z-VAD-FMK (carbobenzoxy-valyl-alanyl-aspartyl-[O-methyl]-fluoro-methyl ketone) on the modulation of the LPS-induced inflammatory response of murine RAW 264.7 cells and primary macrophages was examined. Moreover, the inflammatory responses of human gingival fibroblasts, HSC2 oral squamous carcinoma cells and murine ST2 mesenchymal fibroblasts when exposed to TNFα were studied. Data showed that Z-VAD-FMK significantly lowered the inflammatory response of RAW 264.7 cells and primary macrophages, as indicated by the expression of IL1 and IL6. In murine ST2 mesenchymal fibroblasts, the TNFα-induced expression of CCL2 and CCL5 was significantly reduced. In human gingival fibroblasts and HSC2 cells, Z-VAD-FMK considerably reduced the TNFα-induced expression of CXCL8 and CXCL10. These findings suggest that pharmacological blocking of caspases in an inflammatory environment lowers the expression of cytokines and chemokines in periodontal cells.en
dc.description.affiliationDepartment of Oral Biology University Clinic of Dentistry Medical University of Vienna, Sensengasse 2a
dc.description.affiliationDepartment of Diagnosis and Surgery School of Dentistry São Paulo State University (UNESP), Sao Paulo
dc.description.affiliationCentre for Research on Dental Implants (CEPID) Department of Dentistry Federal University of Santa Catarina (UFSC
dc.description.affiliationDepartment of Periodontology School of Dental Medicine University of Bern, Freiburgstrasse 7
dc.description.affiliationAustrian Cluster for Tissue Regeneration, Donaueschingenstraße 13
dc.description.affiliationUnespDepartment of Diagnosis and Surgery School of Dentistry São Paulo State University (UNESP), Sao Paulo
dc.description.sponsorshipOsteology Foundation
dc.identifierhttp://dx.doi.org/10.3390/life12071045
dc.identifier.citationLife, v. 12, n. 7, 2022.
dc.identifier.doi10.3390/life12071045
dc.identifier.issn2075-1729
dc.identifier.scopus2-s2.0-85136168748
dc.identifier.urihttp://hdl.handle.net/11449/240671
dc.language.isoeng
dc.relation.ispartofLife
dc.sourceScopus
dc.subjectcaspase
dc.subjectfibroblast
dc.subjectin vitro
dc.subjectinflammation
dc.subjectmacrophage
dc.subjectperiodontitis
dc.titleBlocking of Caspases Exerts Anti-Inflammatory Effects on Periodontal Cellsen
dc.typeArtigo
unesp.author.orcid0000-0003-3557-3493[1]
unesp.author.orcid0000-0001-7873-0765[4]

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