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NMR Metabolomics Assessment of Osteogenic Differentiation of Adipose-Tissue-Derived Mesenchymal Stem Cells

[Image: see text] This Article presents, for the first time to our knowledge, an untargeted nuclear magnetic resonance (NMR) metabolomic characterization of the polar intracellular metabolic adaptations of human adipose-derived mesenchymal stem cells during osteogenic differentiation. The use of mes...

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Autores principales: Bispo, Daniela S. C., Jesus, Catarina S. H., Correia, Marlene, Ferreira, Filipa, Bonifazio, Giulia, Goodfellow, Brian J., Oliveira, Mariana B., Mano, João F., Gil, Ana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776527/
https://www.ncbi.nlm.nih.gov/pubmed/35061379
http://dx.doi.org/10.1021/acs.jproteome.1c00832
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author Bispo, Daniela S. C.
Jesus, Catarina S. H.
Correia, Marlene
Ferreira, Filipa
Bonifazio, Giulia
Goodfellow, Brian J.
Oliveira, Mariana B.
Mano, João F.
Gil, Ana M.
author_facet Bispo, Daniela S. C.
Jesus, Catarina S. H.
Correia, Marlene
Ferreira, Filipa
Bonifazio, Giulia
Goodfellow, Brian J.
Oliveira, Mariana B.
Mano, João F.
Gil, Ana M.
author_sort Bispo, Daniela S. C.
collection PubMed
description [Image: see text] This Article presents, for the first time to our knowledge, an untargeted nuclear magnetic resonance (NMR) metabolomic characterization of the polar intracellular metabolic adaptations of human adipose-derived mesenchymal stem cells during osteogenic differentiation. The use of mesenchymal stem cells (MSCs) for bone regeneration is a promising alternative to conventional bone grafts, and untargeted metabolomics may unveil novel metabolic information on the osteogenic differentiation of MSCs, allowing their behavior to be understood and monitored/guided toward effective therapies. Our results unveiled statistically relevant changes in the levels of just over 30 identified metabolites, illustrating a highly dynamic process with significant variations throughout the whole 21-day period of osteogenic differentiation, mainly involving amino acid metabolism and protein synthesis; energy metabolism and the roles of glycolysis, the tricarboxylic acid cycle, and oxidative phosphorylation; cell membrane metabolism; nucleotide metabolism (including the specific involvement of O-glycosylation intermediates and NAD(+)); and metabolic players in protective antioxidative mechanisms (such as glutathione and specific amino acids). Different metabolic stages are proposed and are supported by putative biochemical explanations for the metabolite changes observed. This work lays the groundwork for the use of untargeted NMR metabolomics to find potential metabolic markers of osteogenic differentiation efficacy.
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spelling pubmed-97765272022-12-23 NMR Metabolomics Assessment of Osteogenic Differentiation of Adipose-Tissue-Derived Mesenchymal Stem Cells Bispo, Daniela S. C. Jesus, Catarina S. H. Correia, Marlene Ferreira, Filipa Bonifazio, Giulia Goodfellow, Brian J. Oliveira, Mariana B. Mano, João F. Gil, Ana M. J Proteome Res [Image: see text] This Article presents, for the first time to our knowledge, an untargeted nuclear magnetic resonance (NMR) metabolomic characterization of the polar intracellular metabolic adaptations of human adipose-derived mesenchymal stem cells during osteogenic differentiation. The use of mesenchymal stem cells (MSCs) for bone regeneration is a promising alternative to conventional bone grafts, and untargeted metabolomics may unveil novel metabolic information on the osteogenic differentiation of MSCs, allowing their behavior to be understood and monitored/guided toward effective therapies. Our results unveiled statistically relevant changes in the levels of just over 30 identified metabolites, illustrating a highly dynamic process with significant variations throughout the whole 21-day period of osteogenic differentiation, mainly involving amino acid metabolism and protein synthesis; energy metabolism and the roles of glycolysis, the tricarboxylic acid cycle, and oxidative phosphorylation; cell membrane metabolism; nucleotide metabolism (including the specific involvement of O-glycosylation intermediates and NAD(+)); and metabolic players in protective antioxidative mechanisms (such as glutathione and specific amino acids). Different metabolic stages are proposed and are supported by putative biochemical explanations for the metabolite changes observed. This work lays the groundwork for the use of untargeted NMR metabolomics to find potential metabolic markers of osteogenic differentiation efficacy. American Chemical Society 2022-01-21 2022-03-04 /pmc/articles/PMC9776527/ /pubmed/35061379 http://dx.doi.org/10.1021/acs.jproteome.1c00832 Text en © 2022 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Bispo, Daniela S. C.
Jesus, Catarina S. H.
Correia, Marlene
Ferreira, Filipa
Bonifazio, Giulia
Goodfellow, Brian J.
Oliveira, Mariana B.
Mano, João F.
Gil, Ana M.
NMR Metabolomics Assessment of Osteogenic Differentiation of Adipose-Tissue-Derived Mesenchymal Stem Cells
title NMR Metabolomics Assessment of Osteogenic Differentiation of Adipose-Tissue-Derived Mesenchymal Stem Cells
title_full NMR Metabolomics Assessment of Osteogenic Differentiation of Adipose-Tissue-Derived Mesenchymal Stem Cells
title_fullStr NMR Metabolomics Assessment of Osteogenic Differentiation of Adipose-Tissue-Derived Mesenchymal Stem Cells
title_full_unstemmed NMR Metabolomics Assessment of Osteogenic Differentiation of Adipose-Tissue-Derived Mesenchymal Stem Cells
title_short NMR Metabolomics Assessment of Osteogenic Differentiation of Adipose-Tissue-Derived Mesenchymal Stem Cells
title_sort nmr metabolomics assessment of osteogenic differentiation of adipose-tissue-derived mesenchymal stem cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776527/
https://www.ncbi.nlm.nih.gov/pubmed/35061379
http://dx.doi.org/10.1021/acs.jproteome.1c00832
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