Zou Zhiyuan, Wang Le, Zhou Zhifei, Sun Qing, Liu Delong, Chen Yan, Hu Hao, Cai Yu, Lin Sixiong, Yu Zhengran, Tan Bizhi, Guo Wei, Ling Zemin, Zou Xuenong
Guangdong Provincial Key Laboratory of Orthopaedics and Traumatology, Department of Spine Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China.
Key Laboratory of Functional Polymer Materials, Ministry of Education, Institute of Polymer Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
Bioact Mater. 2020 Dec 7;6(6):1839-1851. doi: 10.1016/j.bioactmat.2020.11.021. eCollection 2021 Jun.
Tissue regeneration based on the utilization of artificial soft materials is considered a promising treatment for bone-related diseases. Here, we report cranial bone regeneration promoted by hydrogels that contain parathyroid hormone (PTH) peptide PTH(1-34) and nano-hydroxyapatite (nHAP). A combination of the positively charged natural polymer chitosan (CS) and negatively charged sodium alginate led to the formation of hydrogels with porous structures, as shown by scanning electron microscopy. Rheological characterizations revealed that the mechanical properties of the hydrogels were almost maintained upon the addition of nHAP and PTH(1-34). In vitro experiments showed that the hydrogel containing nHAP and PTH(1-34) exhibited strong biocompatibility and facilitated osteogenic differentiation of rat bone marrow mesenchymal stem cells (rBMSCs) via the Notch signaling pathway, as shown by the upregulated expression of osteogenic-related proteins. We found that increasing the content of PTH(1-34) in the hydrogels resulted in enhanced osteogenic differentiation of BMSCs. Implantation of the complex hydrogel into a rat cranial defect model led to efficient bone regeneration compared to the rats treated with the hydrogel alone or with nHAP, indicating the simultaneous therapeutic effect of nHAP and PTH during the treatment process. Both the in vitro and in vivo results demonstrated that simultaneously incorporating nHAP and PTH into hydrogels shows promise for bone regeneration, suggesting a new strategy for tissue engineering and regeneration in the future.
基于人工软材料利用的组织再生被认为是治疗骨相关疾病的一种有前景的方法。在此,我们报道了含有甲状旁腺激素(PTH)肽PTH(1 - 34)和纳米羟基磷灰石(nHAP)的水凝胶促进颅骨再生的情况。如扫描电子显微镜所示,带正电荷的天然聚合物壳聚糖(CS)和带负电荷的海藻酸钠相结合导致形成具有多孔结构的水凝胶。流变学表征显示,添加nHAP和PTH(1 - 34)后水凝胶的机械性能几乎保持不变。体外实验表明,含有nHAP和PTH(1 - 34)的水凝胶表现出很强的生物相容性,并通过Notch信号通路促进大鼠骨髓间充质干细胞(rBMSCs)的成骨分化,这通过成骨相关蛋白表达上调得以证明。我们发现增加水凝胶中PTH(1 - 34)的含量会导致BMSCs的成骨分化增强。与单独用水凝胶或nHAP处理的大鼠相比,将复合水凝胶植入大鼠颅骨缺损模型中可实现高效的骨再生,这表明在治疗过程中nHAP和PTH具有协同治疗作用。体外和体内结果均表明,将nHAP和PTH同时掺入水凝胶对骨再生具有前景,为未来的组织工程和再生提供了一种新策略。