Department of Spine Surgery, Hong Hui Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi Province, 710054, China.
Department of Orthopaedic, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province, 510515, China.
Biochem Biophys Res Commun. 2024 Nov 12;733:150714. doi: 10.1016/j.bbrc.2024.150714. Epub 2024 Sep 17.
Reconstruction of bone defects has long been a major clinical challenge. Limited by the various shortcomings of conventional treatment like autologous bone grafting and inorganic substitutes, the development of novel bone repairing strategies is on top priority. Injectable biomimetic hydrogels that deliver stem cells and growth factors in a minimally invasive manner can effectively promote bone regeneration and thus represent a promising alternative. Therefore, in this study, we designed and constructed an injectable nanocomposite hydrogel co-loaded with Laponite (Lap) and vascular endothelial growth factor (VEGF) through a simplified and convenient scheme of physical co-mixing (G@Lap/VEGF). The introduced Lap not only optimized the injectability of GelMA by the electrostatic force between the nanoparticles, but also significantly delayed the release of VEGF-A. In addition, Lap promoted high expression of osteogenic biomarkers in mesenchymal stem cells (MSCs) and enhanced the matrix mineralization. Besides, VEGF-A exerted chemotactic effects recruiting endothelial progenitor cells (EPCs) and inducing neovascularization. Histological and micro-CT results demonstrated that the critical-sized calvarial bone defect lesions in the SD rats after treated with G@Lap/VEGF exhibited significant in vivo bone repairing. In conclusion, the injectable G@Lap/VEGF nanocomposite hydrogel constructed in our study is highly promising for clinical transformation and applications, providing a convenient and simplified scheme for clinical bone repairing, and contributing to the further development of the injectable biomimetic hydrogels.
骨缺损的重建一直是一个主要的临床挑战。受传统治疗方法(如自体骨移植和无机替代品)的各种缺点的限制,新型骨修复策略的发展是当务之急。以微创方式递送干细胞和生长因子的可注射仿生水凝胶可以有效地促进骨再生,因此是一种很有前途的替代方法。因此,在这项研究中,我们通过一种简化方便的物理共混方案(G@Lap/VEGF)设计并构建了一种可注射的纳米复合水凝胶,该水凝胶共载有 Laponite(Lap)和血管内皮生长因子(VEGF)。引入的 Lap 不仅通过纳米颗粒之间的静电力优化了 GelMA 的可注射性,而且还显著延迟了 VEGF-A 的释放。此外,Lap 促进了间充质干细胞(MSCs)中成骨生物标志物的高表达,并增强了基质矿化。此外,VEGF-A 发挥趋化作用招募内皮祖细胞(EPCs)并诱导新血管生成。组织学和 micro-CT 结果表明,SD 大鼠的临界大小颅骨骨缺损病变在经过 G@Lap/VEGF 治疗后表现出显著的体内骨修复。总之,我们在研究中构建的可注射 G@Lap/VEGF 纳米复合水凝胶具有很高的临床转化和应用前景,为临床骨修复提供了一种方便简化的方案,为可注射仿生水凝胶的进一步发展做出了贡献。