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In this study, we used intraperitoneally administered glucose to assess glucose metabolism

Through a variety of routes and enzymatic reprogramming, energy metabolism is switched from glycolysis in the cytosol to OXPHOS in the mitochondria during differentiating ( During the osteogenic differentiation of MSCs, morphological alterations of mitochondria are mainly manifested by enlargement and elongation, and increased volume ( via reducing ROS production by damaged mitochondria, tightening additional energy supply, and producing ATP during degradation ( 2+ homeostasis by increasing cytoplasmic Ca 2+ entry and CaMKII activity, leading to ubiquitin-mediated proteasomal degradation of -Catenin, suggesting that the balance between mitochondrial fusion and division is critical for maintaining Ca 2+ homeostasis ( Going forward, considering the central role of redox balance, metabolic modulation and quality control in regulating bone homeostasis of MSCs, we focused on reviewing therapeutic strategies to promote bone formation based on mitochondrial homeostasis ( Figure 1 )

Improper storage reduces stability over time

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