Magnesium-doped bioactive glass enhances bone regeneration by reversing replicative senescence of human dental pulp stem cells in bone defect therapy

TL;DR

Magnesium-doped bioactive glass reverses aging in dental stem cells, improving their ability to repair bone defects.

Contribution

A magnesium-doped bioactive glass is shown to reverse replicative senescence in human dental pulp stem cells, enhancing their bone regeneration potential.

Findings

20 Mg-BG reverses replicative senescence in hDPSCs by improving mitochondrial function and reducing ROS levels.

20 Mg-BG enhances osteogenic differentiation and bone repair in a rat calvarial defect model.

The IKBKGP1-mediated NF-κB pathway is implicated in the mechanism of action of Mg-BG.

Abstract

Human dental pulp stem cells (hDPSCs) exhibit replicative senescence during in vitro expansion, leading to a reduction in osteogenic differentiation capacity and thereby limiting their potential for bone defect regeneration. Magnesium ion (Mg2+), one of the most abundant divalent cations in the human body, is involved in numerous physiological processes. Mg2+ deficiency has been closely associated with bone fragility and various systemic aging-related diseases, underscoring its critical role in aging and bone metabolism. However, the effects of Mg2+ on mesenchymal stem cells (MSCs) replicative senescence remain poorly understood. In this study, we developed magnesium-doped bioactive glass (Mg-BG) powder with a graded magnesium doping ratio through the sol-gel method, and characterized the pore structure and ion release profiles of each Mg-BG group. We demonstrated that 20 Mg-BG (Mg-BG containing 20 mol% MgO) can effectively reverse the replicative senescence of hDPSCs, improve mitochondrial function, reduce ROS levels and enhance the expression of surface markers associated with differentiation, migration and adhesion in replicatively senescent hDPSCs, thereby enhancing their osteogenic differentiation potential. Furthermore, in vivo experiments using a rat calvarial defect model also confirmed that 20 Mg-BG significantly enhances bone defect repair mediated by replicatively senescent hDPSCs. Mechanistically, we found that the IKBKGP1-mediated NF-κB pathway may play a key role in this process, as revealed by transcriptome sequencing. These findings indicate that Mg-BG could serve as an effective, innovative approach to reverse replicative senescence in hDPSCs and enhance their bone defect repair capabilities.

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