Wang Yi-Rong, Zhang Xiao-Xia, Chen Xu-Xu, Yin Xin-Hua, Yang Ming, Jiang Kuo, Liu Shi-Chang
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration & National Clinical Research Center for Oral Diseases & Shaanxi Key Laboratory of Stomatology, Department of Operative Dentistry & Endodontics, School of Stomatology, The Fourth Military Medical University, Xi'an, Shaanxi, 710032, P. R. China.
Xi'an International University, Xi'an, Shaanxi, 710032, P. R. China.
Adv Healthc Mater. 2025 Jan;14(3):e2401430. doi: 10.1002/adhm.202401430. Epub 2024 Aug 23.
Regenerating bone defects in diabetic rats presents a significant challenge due to the detrimental effects of reactive oxygen species and impaired autophagy on bone healing. To address these issues, a metformin-modified biomimetic silicified collagen scaffold is developed utilizing the principles of biomimetic silicification. In vitro and in vivo experiments demonstrated that the scaffold enhanced bone tissue regeneration within the diabetic microenvironment through the release of dual bio-factors. Further analysis reveals a potential therapeutic mechanism whereby these dual bio-factors synergistically promoted osteogenesis in areas of diabetic bone defects by improving mitochondrial autophagy and maintaining redox balance. The present study provides critical insights into the advancement of tissue engineering strategies aimed at bone regeneration in diabetic patients. The study also sheds light on the underlying biological mechanisms.
由于活性氧和自噬受损对骨愈合的有害影响,糖尿病大鼠的骨缺损再生面临重大挑战。为了解决这些问题,利用仿生硅化原理开发了一种二甲双胍修饰的仿生硅化胶原支架。体外和体内实验表明,该支架通过释放双重生物因子增强了糖尿病微环境中的骨组织再生。进一步分析揭示了一种潜在的治疗机制,即这些双重生物因子通过改善线粒体自噬和维持氧化还原平衡,协同促进糖尿病骨缺损区域的成骨作用。本研究为旨在促进糖尿病患者骨再生的组织工程策略的进展提供了关键见解。该研究还揭示了潜在的生物学机制。