Three-dimensional cell sheet model improves <i>in vitro</i> prediction accuracy of osteogenic potential for biodegradable magnesium-based metals.

Abstract

Biodegradable metals have been increasingly utilized clinically due to their biosafety and pro-osteogenic properties. However, conventional monolayer cell-based preclinical safety evaluation methods based on ISO10993-5 consistently indicate significant cytotoxicity that contradicts <i>in vivo</i> outcomes. In this study, we aimed to establish an <i>in vitro</i> evaluation model that better correlates with <i>in vivo</i> performance. Three-layer BMSC cell sheets were constructed using layer-by-layer assembly. Histological analyses revealed a stable three-dimensional structure with elevated cell-cell interaction proteins, including N-Cadherin, Fibronectin, and Vinculin, along with enhanced osteogenic potential. The cytotoxicity of 4N pure Mg was evaluated in both cell sheet and monolayer co-culture models. Flow cytometry showed higher Ki67 expression and lower ROS levels and apoptosis rate in cell sheets. ShRNA-mediated silencing of N-Cadherin in cell sheets significantly compromised their cytoprotective capacity against Mg metal-induced toxicity. Osteogenesis-related gene expression correlation analysis between <i>in vitro</i> co-culture models and <i>in vivo</i> femur implantation models was conducted using RNA-seq and qRT-PCR. Results showed that 4N pure Mg enhanced osteogenic genes (<i>BMP2R</i>, <i>RUNX2</i>, and <i>SP7</i>) in cell sheets, consistent with <i>in vivo</i> patterns but contrary to monolayer models. Various Mg-based metals (4N/5N Pure Mg, ZE21B, and WE43) were evaluated in cell sheet defect, monolayer defect, and cranial defect models. 5N Pure Mg, ZE21B, and WE43 promoted defect healing in both cranial defect and cell sheets, but showed no positive effect in monolayers. Collectively, cell sheet models correlated well with <i>in vivo</i> results, suggesting their potential as alternative <i>in vitro</i> evaluation models, thereby accelerating clinical translation of Mg-based biomaterials.