Publication
Cartilage acidic protein 1 promotes increased cell viability, cell proliferation and energy metabolism in primary human dermal fibroblasts
dc.contributor.author | Letsiou, Sophia | |
dc.contributor.author | Félix, Rute | |
dc.contributor.author | Cardoso, João CR | |
dc.contributor.author | L, Anjos | |
dc.contributor.author | Mestre, Ana L G | |
dc.contributor.author | H, Gomes | |
dc.contributor.author | Power, Deborah | |
dc.date.accessioned | 2021-06-24T11:35:46Z | |
dc.date.available | 2021-06-24T11:35:46Z | |
dc.date.issued | 2020-04 | |
dc.description.abstract | Cartilage acidic protein 1 (CRTAC1) is an extracellular matrix protein of human chondrogenic tissue that is also present in other vertebrates, non-vertebrate eukaryotes and in some prokaryotes. The function of CRTAC1 remains unknown but the protein's structure indicates a role in cell-cell or cell-matrix interactions and calcium-binding. The aim of the present study was to evaluate the in vitro effects of hCRTAC1-A on normal human dermal fibroblasts (NHDF). A battery of in vitro assays (biochemical and PCR), immunofluorescence and a biosensor approach were used to characterize the protein's biological activities on NHDF cells in a scratch assay. Gene expression analysis revealed that hCRTAC1-A protein is associated with altered levels of expression for genes involved in the processes of cell proliferation (CXCL12 and NOS2), cell migration (AQP3 and TNC), and extracellular matrix-ECM regeneration and remodeling (FMOD, TIMP1, FN1) indicating a role for hCRTAC1-A in promoting these activities in a scratch assay. In parallel, the candidate processes identified by differential gene transcription were substantiated and extended using Electric cell-substrate impedance sensing (ECIS) technology, immunofluorescence and cell viability assays. Our findings indicate that hCRTAC1-A stimulated cell proliferation, migration and ECM production in primary human fibroblasts in vitro. (C) 2020 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved. | |
dc.description.sponsorship | H2020-MSCA-RISE-2015 | |
dc.description.sponsorship | ALGAE4A-B [691102] | |
dc.description.sponsorship | EMBRIC (European Union's Horizon 2020 research and innovation programme) [654008] | |
dc.description.sponsorship | Portuguese Foundation for Science and Technology (FCT)Portuguese Foundation for Science and Technology [UIDB/04326/2020] | |
dc.description.sponsorship | operational programme CRESC Algarve 2020 [EMBRC.PT ALG-01-0145-FEDER-022121] | |
dc.description.sponsorship | operational programme COMPETE 2020 [EMBRC.PT ALG-01-0145-FEDER-022121] | |
dc.description.sponsorship | FCTPortuguese Foundation for Science and TechnologyEuropean Commission [UIDB/04326/2020, DL57/2016/CP1361, CT0020, CT0011] | |
dc.description.version | info:eu-repo/semantics/publishedVersion | |
dc.identifier.doi | 10.1016/j.biochi.2020.02.008 | |
dc.identifier.issn | 0300-9084 | |
dc.identifier.uri | http://hdl.handle.net/10400.1/16532 | |
dc.language.iso | eng | |
dc.peerreviewed | yes | |
dc.publisher | Elsevier | |
dc.subject | ECIS biosensor | |
dc.subject | Cell migration | |
dc.subject | Cell proliferation | |
dc.subject | hCRTAC1 | |
dc.subject | In vitro scratch assay | |
dc.subject | Primary human fibroblasts | |
dc.title | Cartilage acidic protein 1 promotes increased cell viability, cell proliferation and energy metabolism in primary human dermal fibroblasts | |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.endPage | 78 | |
oaire.citation.startPage | 72 | |
oaire.citation.title | Biochimie | |
oaire.citation.volume | 171 | |
person.familyName | Félix | |
person.familyName | Cardoso | |
person.familyName | Anjos Guerreiro | |
person.familyName | Mestre | |
person.familyName | Gomes | |
person.familyName | Power | |
person.givenName | Rute | |
person.givenName | João | |
person.givenName | Liliana Isabel Tomé | |
person.givenName | Ana | |
person.givenName | Henrique Leonel | |
person.givenName | Deborah Mary | |
person.identifier | 14332 | |
person.identifier | AAK-3800-2020 | |
person.identifier.ciencia-id | FB1A-1325-8E25 | |
person.identifier.ciencia-id | 8B16-F203-2AFC | |
person.identifier.ciencia-id | 6D18-2D1C-A45C | |
person.identifier.ciencia-id | 601B-4B7D-ABC3 | |
person.identifier.ciencia-id | 891A-8A44-3CAE | |
person.identifier.orcid | 0000-0002-4144-3452 | |
person.identifier.orcid | 0000-0001-7890-0170 | |
person.identifier.orcid | 0000-0001-9474-522X | |
person.identifier.orcid | 0000-0002-6679-8698 | |
person.identifier.orcid | 0000-0003-3664-4740 | |
person.identifier.orcid | 0000-0003-1366-0246 | |
person.identifier.rid | M-6164-2013 | |
person.identifier.rid | M-4151-2013 | |
person.identifier.scopus-author-id | 56006773000 | |
person.identifier.scopus-author-id | 7201822956 | |
person.identifier.scopus-author-id | 8575757700 | |
person.identifier.scopus-author-id | 7005305880 | |
person.identifier.scopus-author-id | 7101806760 | |
rcaap.rights | restrictedAccess | |
rcaap.type | article | |
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relation.isAuthorOfPublication.latestForDiscovery | 6da677b9-927f-423d-8657-448a0dccb67c |
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