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dc.contributor.authorRocha Loureda, Beatriz
dc.contributor.authorCillero Pastor, Berta 
dc.contributor.authorEijkel, Gert
dc.contributor.authorCalamia, Valentina
dc.contributor.authorFernández Puente, Patricia 
dc.contributor.authorPaine, Martin R L
dc.contributor.authorRuiz Romero, Cristina 
dc.contributor.authorHeeren, Ron M A
dc.contributor.authorBLANCO GARCIA, FRANCISCO JAVIER 
dc.date.accessioned2022-03-04T07:46:23Z
dc.date.available2022-03-04T07:46:23Z
dc.date.issued2020
dc.identifier.issn1535-9476
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31980557es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16159
dc.description.abstractIn osteoarthritis (OA), impairment of cartilage regeneration can be related to a defective chondrogenic differentiation of mesenchymal stromal cells (MSCs). Therefore, understanding the proteomic- and metabolomic-associated molecular events during the chondrogenesis of MSCs could provide alternative targets for therapeutic intervention. Here, a SILAC-based proteomic analysis identified 43 proteins related with metabolic pathways whose abundance was significantly altered during the chondrogenesis of OA human bone marrow MSCs (hBMSCs). Then, the level and distribution of metabolites was analyzed in these cells and healthy controls by matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI), leading to the recognition of characteristic metabolomic profiles at the early stages of differentiation. Finally, integrative pathway analysis showed that UDP-glucuronic acid synthesis and amino sugar metabolism were downregulated in OA hBMSCs during chondrogenesis compared with healthy cells. Alterations in these metabolic pathways may disturb the production of hyaluronic acid (HA) and other relevant cartilage extracellular matrix (ECM) components. This work provides a novel integrative insight into the molecular alterations of osteoarthritic MSCs and potential therapeutic targets for OA drug development through the enhancement of chondrogenesis.en
dc.language.isoenes
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshHumans*
dc.subject.meshChondrogenesis*
dc.subject.meshPentose Phosphate Pathway*
dc.subject.meshMetabolome*
dc.subject.meshCase-Control Studies*
dc.subject.meshUridine Diphosphate Glucuronic Acid*
dc.subject.meshOsteoarthritis*
dc.titleIntegrative Metabolic Pathway Analysis Reveals Novel Therapeutic Targets in Osteoarthritisen
dc.typeJournal Articlees
dc.authorsophosRocha, Beatriz;Cillero-Pastor, Berta;Eijkel, Gert;Calamia, Valentina;Fernandez-Puente, Patricia;Paine, Martin R L;Ruiz-Romero, Cristina;Heeren, Ron M A;Blanco, Francisco J
dc.identifier.doi10.1074/mcp.RA119.001821
dc.identifier.pmid31980557
dc.identifier.sophos35578
dc.issue.number4es
dc.journal.titleMOLECULAR & CELLULAR PROTEOMICSes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario de A Coruña::Reumatoloxía
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Biomédica da Coruña
dc.relation.publisherversionhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7124476/pdf/zjw574.pdfes
dc.rights.accessRightsopenAccess
dc.subject.decsestudios de casos y controles *
dc.subject.decsmetaboloma *
dc.subject.decsvía de la pentosa-fosfato *
dc.subject.decshumanos *
dc.subject.decsuridina difosfato del ácido glucurónico *
dc.subject.decsosteoartritis *
dc.subject.decscondrogénesis *
dc.subject.keywordCHUACes
dc.subject.keywordINIBIC
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number19es


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Atribución 4.0 Internacional
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