TY - JOUR
T1 - Metabolic and transcriptional changes across osteogenic differentiation of mesenchymal stromal cells
AU - Sigmarsdottir, Thora Bjorg
AU - McGarrity, Sarah
AU - de Lomana, Adrián López García
AU - Kotronoulas, Aristotelis
AU - Sigurðsson, Snaevar
AU - Yurkovich, James T.
AU - Rolfsson, Ottar
AU - Sigurjonsson, Olafur Eysteinn
AU - Sigurdsson, Snaevar
N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).
PY - 2021/12/10
Y1 - 2021/12/10
N2 - Mesenchymal stromal cells (MSCs) are multipotent post-natal stem cells with applications in tissue engineering and regenerative medicine. MSCs can differentiate into osteoblasts, chondrocytes, or adipocytes, with functional differences in cells during osteogenesis accompanied by metabolic changes. The temporal dynamics of these metabolic shifts have not yet been fully characterized and are suspected to be important for therapeutic applications such as osteogenesis optimization. Here, our goal was to characterize the metabolic shifts that occur during osteogenesis. We profiled five key extracellular metabolites longitudinally (glucose, lactate, glutamine, glutamate, and ammonia) from MSCs from four donors to classify osteogenic differentiation into three metabolic stages, defined by changes in the uptake and secretion rates of the metabolites in cell culture media. We used a combination of untargeted metabolomic analysis, targeted analysis of13C-glucose labelled intracellular data, and RNA-sequencing data to reconstruct a gene regulatory network and further characterize cellular metabolism. The metabolic stages identified in this proof-of-concept study provide a framework for more detailed investigations aimed at identifying biomarkers of osteogenic differentiation and small molecule interventions to optimize MSC differentiation for clinical applications.
AB - Mesenchymal stromal cells (MSCs) are multipotent post-natal stem cells with applications in tissue engineering and regenerative medicine. MSCs can differentiate into osteoblasts, chondrocytes, or adipocytes, with functional differences in cells during osteogenesis accompanied by metabolic changes. The temporal dynamics of these metabolic shifts have not yet been fully characterized and are suspected to be important for therapeutic applications such as osteogenesis optimization. Here, our goal was to characterize the metabolic shifts that occur during osteogenesis. We profiled five key extracellular metabolites longitudinally (glucose, lactate, glutamine, glutamate, and ammonia) from MSCs from four donors to classify osteogenic differentiation into three metabolic stages, defined by changes in the uptake and secretion rates of the metabolites in cell culture media. We used a combination of untargeted metabolomic analysis, targeted analysis of13C-glucose labelled intracellular data, and RNA-sequencing data to reconstruct a gene regulatory network and further characterize cellular metabolism. The metabolic stages identified in this proof-of-concept study provide a framework for more detailed investigations aimed at identifying biomarkers of osteogenic differentiation and small molecule interventions to optimize MSC differentiation for clinical applications.
KW - Mesenchymal Stem Cells
KW - gene regulatory network
KW - glycolysis
KW - mesenchymal stromal cells (MSCs)
KW - metabolic changes
KW - metabolism
KW - metabolites
KW - osteogenic differentiation
KW - oxidative phosphorylation
KW - Gene regulatory network
KW - Glycolysis
KW - Mesenchymal Stem Cells
KW - Mesenchymal stromal cells (MSCs)
KW - Metabolic changes
KW - Metabolism
KW - Metabolites
KW - Osteogenic differentiation
KW - Oxidative phosphorylation
UR - https://www.scopus.com/pages/publications/85121266779
U2 - 10.3390/bioengineering8120208
DO - 10.3390/bioengineering8120208
M3 - Article
C2 - 34940360
SN - 2306-5354
VL - 8
JO - Bioengineering
JF - Bioengineering
IS - 12
M1 - 208
ER -