Influence of redox stress on crosstalk between fibroblasts and keratinocytes

dc.bibliographicCitation.firstPage1338
dc.bibliographicCitation.issue12
dc.bibliographicCitation.volume10
dc.contributor.authorBhartiya, Pradeep
dc.contributor.authorMasur, Kai
dc.contributor.authorShome, Debarati
dc.contributor.authorKaushik, Neha
dc.contributor.authorNguyen, Linh N.
dc.contributor.authorKaushik, Nagendra Kumar
dc.contributor.authorChoi, Eun Ha
dc.date.accessioned2023-05-22T07:20:02Z
dc.date.available2023-05-22T07:20:02Z
dc.date.issued2021
dc.description.abstractAlthough the skin is constantly subjected to endogenous and exogenous stress, it maintains a homeostatic state through wound repair and regeneration pathways. Treatment for skin diseases and injury requires a significant understanding of the various mechanisms and interactions that occur within skin cells. Keratinocytes and fibroblasts interact with each other and act as key players in the repair process. Although fibroblasts and keratinocytes are widely studied in wound healing and skin remodeling under different conditions, the influence of redox stress on keratinocyte-fibroblast crosstalk has not been thoroughly investigated. In this study, we used cold atmospheric plasma (CAP) to generate and deliver oxidative stress to keratinocytes and fibroblasts and to assess its impact on their interactions. To this end, we used a well-established in vitro 3D co-culture model imitating a realistic scenario. Our study shows that low CAP exposure is biocompatible and does not affect the viability or energetics of fibroblasts and keratinocytes. Exposure to low doses of CAP enhanced the proliferation rate of cells and stimulated the expression of key genes (KGF, MMP2, GMCSF, IL-6, and IL-8) in fibroblasts, indicating the activation and initiation of the skin repair process. Additionally, enhanced migration was observed under co-culture conditions under the given redox stress conditions, and expression of the upstream regulator and the effectors of the Hippo pathway (YAP and CYR61, respectively), which are associated with enhanced migration, were elevated. Overall, this study reinforces the application of CAP and redox stress in skin repair physiology.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/12157
dc.identifier.urihttp://dx.doi.org/10.34657/11190
dc.language.isoeng
dc.publisherBasel : MDPI
dc.relation.doihttps://doi.org/10.3390/biology10121338
dc.relation.essn2079-7737
dc.relation.ispartofseriesBiology 10 (2021), Nr. 12eng
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectCell migrationeng
dc.subjectPhysical plasmaeng
dc.subjectSkin homeostasiseng
dc.subject.ddc570
dc.titleInfluence of redox stress on crosstalk between fibroblasts and keratinocyteseng
dc.typearticle
dc.typeText
dcterms.bibliographicCitation.journalTitleBiology
tib.accessRightsopenAccess
wgl.contributorINP
wgl.subjectBiowissenschaften/Biologieger
wgl.typeZeitschriftenartikelger
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
biology-10-01338.pdf
Size:
2.86 MB
Format:
Adobe Portable Document Format
Description: