Li Jian, Zhang Xu, Peng Zi-Xin, Chen Jian-Hai, Liang Jian-Hui, Ke Li-Qing, Huang Dan, Cheng Wen-Xiang, Lin Sien, Li Gang, Hou Rui, Zhong Wen-Zhao, Lin Zheng-Jie, Qin Ling, Chen Guo-Qiang, Zhang Peng
Center for Translational Medicine Research and Development, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong 518055, China; Faculty of Biomedical Engineering, Shenzhen University of Advanced Technology, Shenzhen, Guangdong 518055, China.
National Center of Stomatology, National Clinical Research Center for Oral Diseases, National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, Beijing Key Laboratory of Digital Stomatology, Center of Digital Dentistry, Peking University School and Hospital of Stomatology, Beijing 100081, China.
Trends Biotechnol. 2024 Dec;42(12):1745-1776. doi: 10.1016/j.tibtech.2024.08.002. Epub 2024 Sep 5.
The understanding of cellular energy metabolism activation by engineered scaffolds remains limited, posing challenges for therapeutic applications in tissue regeneration. This study presents biosynthesized poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3HB-co-4HB)] and its major degradation product, 3-hydroxybutyrate (3HB), as endogenous bioenergetic fuels that augment cellular anabolism, thereby facilitating the progression of human bone marrow-derived mesenchymal stem cells (hBMSCs) towards osteoblastogenesis. Our research demonstrated that 3HB markedly boosts in vitro ATP production, elevating mitochondrial membrane potential and capillary-like tube formation. Additionally, it raises citrate levels in the tricarboxylic acid (TCA) cycle, facilitating the synthesis of citrate-containing apatite during hBMSCs osteogenesis. Furthermore, 3HB administration significantly increased bone mass in rats with osteoporosis induced by ovariectomy. The findings also showed that P(3HB-co-4HB) scaffold substantially enhances long-term vascularized bone regeneration in rat cranial defect models. These findings reveal a previously unknown role of 3HB in promoting osteogenesis of hBMSCs and highlight the metabolic activation of P(3HB-co-4HB) scaffold for bone regeneration.
目前,对于工程支架激活细胞能量代谢的理解仍然有限,这给组织再生的治疗应用带来了挑战。本研究展示了生物合成的聚(3-羟基丁酸酯-共-4-羟基丁酸酯)[P(3HB-co-4HB)]及其主要降解产物3-羟基丁酸(3HB)作为内源性生物能量燃料,可增强细胞合成代谢,从而促进人骨髓间充质干细胞(hBMSCs)向成骨细胞分化。我们的研究表明,3HB显著提高体外ATP生成,提升线粒体膜电位并促进毛细血管样管形成。此外,它还提高三羧酸(TCA)循环中的柠檬酸水平,有助于hBMSCs成骨过程中含柠檬酸磷灰石的合成。此外,给予3HB可显著增加去卵巢诱导的骨质疏松大鼠的骨量。研究结果还表明,P(3HB-co-4HB)支架可显著促进大鼠颅骨缺损模型中长期血管化骨再生。这些发现揭示了3HB在促进hBMSCs成骨方面以前未知的作用,并突出了P(3HB-co-4HB)支架对骨再生的代谢激活作用。