Department of Orthopedics, Nanfang Hospital, Southern Medical University, 1838 # Guangzhou North Avenue, Guangzhou, Guangdong Province 510515, People's Republic of China.
Department of Orthopedics, Nanfang Hospital, Southern Medical University, 1838 # Guangzhou North Avenue, Guangzhou, Guangdong Province 510515, People's Republic of China.
Int J Biol Macromol. 2024 Jun;271(Pt 2):132742. doi: 10.1016/j.ijbiomac.2024.132742. Epub 2024 May 30.
Injectable hydrogels, offering adaptable drug delivery of growth factors (GFs), hold promise for treating bone defects. To optimize osteogenic efficacy, the release of GFs should mirror the natural bone healing. We developed an injectable thermo-responsive hydrogel/microgels platform for dual GF delivery for bone regeneration. Stromal cell-derived factor-1 alpha (SDF-1a) and the Methacrylate Gelatin (GelMA) microgels which encapsulated insulin-like growth factor-1 (IGF-1) loaded liposomes (Ls) were introduced into Poloxamer 407 (P407) hydrogel matrix. This system achieved the biomimetic release profile of SDF-1a and IGF-1, which covered the early stage from day 1 to 7 and the continuous stage from day 5 to 21, respectively. In vitro study confirmed the enhanced migration, osteogenic biomarker expression, and matrix mineralization of the bone marrow mesenchymal stem cells (BMSCs) co-cultivated with the dual GFs delivering hydrogel/microgels. Transcriptome sequencing revealed that the potential mechanism was associated with mitogen-activated protein kinase (MAPK) signaling activation and its downstream ribosomal protein S6 kinase 2 (RSK2) upregulation. In a critical-sized calvarial defect model in Sprague-Dawley (SD) rats, the injectable hydrogel/microgels system promoted significant bone regeneration. Collectively, our study suggested the current hydrogel/microgels system with the biomimetic release of SDF-1a and IGF-1 efficiently promoted bone regeneration, informing the future development of GF delivery systems intended for bone regeneration therapies.
可注射水凝胶可实现生长因子(GFs)的适应性药物传递,有望用于治疗骨缺损。为了优化成骨疗效,GFs 的释放应模仿自然骨愈合过程。我们开发了一种可注射的温敏水凝胶/微凝胶平台,用于骨再生的双重 GF 传递。基质细胞衍生因子 1 阿尔法(SDF-1a)和包载胰岛素样生长因子-1(IGF-1)的明胶(GelMA)微凝胶被引入泊洛沙姆 407(P407)水凝胶基质中。该系统实现了 SDF-1a 和 IGF-1 的仿生释放模式,分别覆盖了第 1 天至第 7 天的早期阶段和第 5 天至第 21 天的持续阶段。体外研究证实,共培养双 GFs 传递水凝胶/微凝胶的骨髓间充质干细胞(BMSCs)的迁移、成骨生物标志物表达和基质矿化得到增强。转录组测序显示,潜在的机制与丝裂原活化蛋白激酶(MAPK)信号通路的激活及其下游核糖体蛋白 S6 激酶 2(RSK2)的上调有关。在 Sprague-Dawley(SD)大鼠的临界尺寸颅骨缺损模型中,可注射水凝胶/微凝胶系统促进了显著的骨再生。总之,我们的研究表明,当前具有 SDF-1a 和 IGF-1 仿生释放的水凝胶/微凝胶系统可有效促进骨再生,为未来用于骨再生治疗的 GF 传递系统的发展提供了信息。