Energy Metabolism in Mesenchymal Stem Cells During Osteogenic Differentiation

There is emerging interest in stem cell energy metabolism and its effect on differentiation. Bioenergetic changes in differentiating bone marrow mesenchymal stem cells (MSCs) are poorly understood and were the focus of our study. Using bioenergetic profiling and transcriptomics, we have established...

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Published inStem cells and development Vol. 25; no. 2; p. 114
Main Authors Shum, Laura C, White, Noelle S, Mills, Bradley N, Bentley, Karen L de Mesy, Eliseev, Roman A
Format Journal Article
LanguageEnglish
Published United States 15.01.2016
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Abstract There is emerging interest in stem cell energy metabolism and its effect on differentiation. Bioenergetic changes in differentiating bone marrow mesenchymal stem cells (MSCs) are poorly understood and were the focus of our study. Using bioenergetic profiling and transcriptomics, we have established that MSCs activate the mitochondrial process of oxidative phosphorylation (OxPhos) during osteogenic differentiation, but they maintain levels of glycolysis similar to undifferentiated cells. Consistent with their glycolytic phenotype, undifferentiated MSCs have high levels of hypoxia-inducible factor 1 (HIF-1). Osteogenically induced MSCs downregulate HIF-1 and this downregulation is required for activation of OxPhos. In summary, our work provides important insights on MSC bioenergetics and proposes a HIF-based mechanism of regulation of mitochondrial OxPhos in MSCs.
AbstractList There is emerging interest in stem cell energy metabolism and its effect on differentiation. Bioenergetic changes in differentiating bone marrow mesenchymal stem cells (MSCs) are poorly understood and were the focus of our study. Using bioenergetic profiling and transcriptomics, we have established that MSCs activate the mitochondrial process of oxidative phosphorylation (OxPhos) during osteogenic differentiation, but they maintain levels of glycolysis similar to undifferentiated cells. Consistent with their glycolytic phenotype, undifferentiated MSCs have high levels of hypoxia-inducible factor 1 (HIF-1). Osteogenically induced MSCs downregulate HIF-1 and this downregulation is required for activation of OxPhos. In summary, our work provides important insights on MSC bioenergetics and proposes a HIF-based mechanism of regulation of mitochondrial OxPhos in MSCs.
Author Eliseev, Roman A
Bentley, Karen L de Mesy
White, Noelle S
Mills, Bradley N
Shum, Laura C
Author_xml – sequence: 1
  givenname: Laura C
  surname: Shum
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  organization: 1 Center for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry , Rochester, New York
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  givenname: Noelle S
  surname: White
  fullname: White, Noelle S
  organization: 1 Center for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry , Rochester, New York
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  givenname: Bradley N
  surname: Mills
  fullname: Mills, Bradley N
  organization: 2 Department of Neurology, University of Rochester School of Medicine and Dentistry , Rochester, New York
– sequence: 4
  givenname: Karen L de Mesy
  surname: Bentley
  fullname: Bentley, Karen L de Mesy
  organization: 3 Department of Pathology, University of Rochester School of Medicine and Dentistry , Rochester, New York
– sequence: 5
  givenname: Roman A
  surname: Eliseev
  fullname: Eliseev, Roman A
  organization: 3 Department of Pathology, University of Rochester School of Medicine and Dentistry , Rochester, New York
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26487485$$D View this record in MEDLINE/PubMed
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Snippet There is emerging interest in stem cell energy metabolism and its effect on differentiation. Bioenergetic changes in differentiating bone marrow mesenchymal...
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SubjectTerms Bone Marrow Cells - cytology
Cell Differentiation - physiology
Cell Proliferation - physiology
Cells, Cultured
Energy Metabolism - physiology
Humans
Hypoxia-Inducible Factor 1, alpha Subunit - metabolism
Mesenchymal Stem Cells - metabolism
Mitochondria - metabolism
Osteogenesis - physiology
Title Energy Metabolism in Mesenchymal Stem Cells During Osteogenic Differentiation
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