Metabolic and Transcriptional Changes across Osteogenic Differentiation of Mesenchymal Stromal Cells

被引:8
|
作者
Sigmarsdottir, Thora Bjorg [1 ]
McGarrity, Sarah [1 ,2 ]
de Lomana, Adrian Lopez Garcia [2 ]
Kotronoulas, Aristotelis [2 ]
Sigurdsson, Snaevar [3 ]
Yurkovich, James T. [4 ]
Rolfsson, Ottar [2 ]
Sigurjonsson, Olafur Eysteinn [1 ,5 ]
机构
[1] Reykjavik Univ, Sch Sci & Engn, IS-101 Reykjavik, Iceland
[2] Univ Iceland, Ctr Syst Biol, IS-101 Reykjavik, Iceland
[3] Univ Iceland, Biomed Ctr, IS-101 Reykjavik, Iceland
[4] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[5] Landspitali Natl Univ Hosp Iceland, Dept RnD, Blood Blank, IS-101 Reykjavik, Iceland
来源
BIOENGINEERING-BASEL | 2021年 / 8卷 / 12期
基金
芬兰科学院;
关键词
mesenchymal stromal cells (MSCs); osteogenic differentiation; metabolites; metabolism; metabolic changes; glycolysis; oxidative phosphorylation; gene regulatory network;
D O I
10.3390/bioengineering8120208
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 of C-13-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.
引用
收藏
页数:27
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