Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/35645
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dc.contributor.authorBispo, Daniela S. C.pt_PT
dc.contributor.authorMichálková, Lenkapt_PT
dc.contributor.authorCorreia, Marlenept_PT
dc.contributor.authorJesus, Catarina S. H.pt_PT
dc.contributor.authorDuarte, Iola F.pt_PT
dc.contributor.authorGoodfellow, Brian J.pt_PT
dc.contributor.authorOliveira, Mariana B.pt_PT
dc.contributor.authorMano, João F.pt_PT
dc.contributor.authorGil, Ana M.pt_PT
dc.date.accessioned2023-01-05T15:56:18Z-
dc.date.available2023-01-05T15:56:18Z-
dc.date.issued2022-04-07-
dc.identifier.urihttp://hdl.handle.net/10773/35645-
dc.description.abstractThis paper describes, for the first time to our knowledge, a lipidome and exometabolome characterization of osteogenic differentiation for human adipose tissue stem cells (hAMSCs) using nuclear magnetic resonance (NMR) spectroscopy. The holistic nature of NMR enabled the time-course evolution of cholesterol, mono- and polyunsaturated fatty acids (including ω-6 and ω-3 fatty acids), several phospholipids (phosphatidylcholine, phosphatidylethanolamine, sphingomyelins, and plasmalogens), and mono- and triglycerides to be followed. Lipid changes occurred almost exclusively between days 1 and 7, followed by a tendency for lipidome stabilization after day 7. On average, phospholipids and longer and more unsaturated fatty acids increased up to day 7, probably related to plasma membrane fluidity. Articulation of lipidome changes with previously reported polar endometabolome profiling and with exometabolome changes reported here in the same cells, enabled important correlations to be established during hAMSC osteogenic differentiation. Our results supported hypotheses related to the dynamics of membrane remodelling, anti-oxidative mechanisms, protein synthesis, and energy metabolism. Importantly, the observation of specific up-taken or excreted metabolites paves the way for the identification of potential osteoinductive metabolites useful for optimized osteogenic protocols.pt_PT
dc.language.isoengpt_PT
dc.publisherMDPIpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC%2FBTM-ORG%2F28835%2F2017/PTpt_PT
dc.relationPOCI-01-0145-FEDER-028835pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/OE/SFRH%2FBD%2F150655%2F2020/PTpt_PT
dc.relationERC-2019-ADG-883370pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/CEEC IND 2017/CEECIND%2F03605%2F2017%2FCP1459%2FCT0044/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50011%2F2020/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50011%2F2020/PTpt_PT
dc.relationLA/P/0006/2020pt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectMesenchymal stem cellspt_PT
dc.subjectOsteogenic differentiationpt_PT
dc.subjectOsteogenesispt_PT
dc.subjectNMR spectroscopypt_PT
dc.subjectMetabolomicspt_PT
dc.subjectLipidomicspt_PT
dc.subjectEndometabolomept_PT
dc.subjectExometabolomept_PT
dc.titleEndo- and exometabolome crosstalk in mesenchymal stem cells undergoing osteogenic differentiationpt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.issue8pt_PT
degois.publication.titleCellspt_PT
degois.publication.volume11pt_PT
dc.relation.publisherversionhttps://www.mdpi.com/2073-4409/11/8/1257pt_PT
dc.identifier.doi10.3390/cells11081257pt_PT
dc.identifier.essn2073-4409pt_PT
dc.identifier.articlenumber1257pt_PT
Appears in Collections:CICECO - Artigos
DQ - Artigos

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