The exosomal secretomes of mesenchymal stem cells extracted via 3D-printed lithium-doped calcium silicate scaffolds promote osteochondral regeneration

• Published in: Materials today bio 2023-10, Vol.22, p.100728-100728, Article 100728
• Main Authors: Lin, Tsung-Li, Lin, Yen-Hong, Lee, Alvin Kai-Xing, Kuo, Ting-You, Chen, Cheng-Yu, Chen, Kun-Hao, Chou, Yun-Ting, Chen, Yi-Wen, Shie, Ming-You
• Format: Article
• Language: English
• Subjects: 3D scaffold; Additive manufacture; Calcium silicate; Exosomes; Full Length; Lithium; Osteochondral defect
• ISSN: 2590-0064; 2590-0064
• DOI: 10.1016/j.mtbio.2023.100728

The development of surface modification techniques has brought about a major paradigm shift in the clinical applications of bone tissue regeneration. Biofabrication strategies enable the creation of scaffolds with specific microstructural environments and biological components. Lithium (Li) has been reported to exhibit anti-inflammatory, osteogenic, and chondrogenic properties by promoting several intracellular signaling pathways. Currently, research focuses on fabricating scaffolds with simultaneous dual bioactivities to enhance osteochondral regeneration. In this study, we modified the surface of calcium silicate (CS) scaffolds with Li using a simple immersion technique and evaluated their capabilities for bone regeneration. The results showed that Li ions could be easily coated onto the surfaces of CS scaffolds without affecting the microstructural properties of CS itself. Furthermore, the modifications did not affect the printing capabilities of the CS, and porous scaffolds could be fabricated via extrusion. Moreover, the presence of Li improved the surface roughness and hydrophilicity, thus leading to enhanced secretion of osteochondral-related regeneration factors, such as alkaline phosphatase (ALP), bone sialoprotein (BSP), and collagen II (Col II) proteins. Subsequent in vivo studies, including histological and micro-CT analyses, confirmed that the Li-modified CS scaffolds promoted osteochondral regeneration. The transcriptome analysis suggested that the enhanced osteochondrogenic capabilities of our scaffolds were influenced by paracrine exosomes. We hope this study will inspire further research on osteochondral regeneration. [Display omitted]