Chen Wei, Chen Hao, Zheng Dandan, Zhang Hongbo, Deng Lianfu, Cui Wenguo, Zhang Yuhui, Santos Hélder A, Shen Hongxing
Department of Spine Surgery Renji Hospital Shanghai JiaoTong University School of Medicine 160 Pujian Road Shanghai 200127 P. R. China.
Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 P. R. China.
Adv Sci (Weinh). 2019 Oct 7;7(1):1902099. doi: 10.1002/advs.201902099. eCollection 2020 Jan.
Gene therapy provides an ideal potential treatment for intervertebral disk degeneration by delivering synthetic microRNAs (miRNAs) to regulate the gene expression levels. However, it is very challenging to deliver miRNAs directly, which leads to inactivation, low transfection efficiency, and short half-life. Here, Agomir is loaded in hydrogel to construct a gene-hydrogel microenvironment for regulating the synthesis/catabolism balance of the tissue extracellular matrix (ECM) to treat degenerative diseases. Agomir is a cholesterol-, methylation-, and phosphorothioate-modified miRNA, which can mimic the function of miRNA to regulate the expression of the target gene. Agomir874 that mimics miRNA874 is synthesized to down regulate the expression of matrix metalloproteinases (MMPs) in nucleus pulposus (NP). At the same time, a polyethylene glycol (PEG) hydrogel is synthesized through Ag-S coordination of 4-arm PEG-SH and silver ion solution, which has injectable, self-healing, antimicrobial, degradable, and superabsorbent properties and matches perfectly with the mechanism of intervertebral disk. By delivering Agomir-loaded PEG-hydrogel to a degenerative intervertebral disk, a gene-hydrogel microenvironment is constructed in situ, which reduces the expression of MMPs, regulates the synthesis/catabolism balance of ECM in the NP of the intervertebral disk, and improves the tissue microenvironment regeneration.
基因治疗通过递送合成微小RNA(miRNA)来调节基因表达水平,为椎间盘退变提供了一种理想的潜在治疗方法。然而,直接递送miRNA极具挑战性,这会导致其失活、转染效率低以及半衰期短。在此,将阿戈美拉汀(Agomir)负载于水凝胶中,构建一种基因 - 水凝胶微环境,以调节组织细胞外基质(ECM)的合成/分解代谢平衡,从而治疗退行性疾病。阿戈美拉汀是一种经胆固醇、甲基化和硫代磷酸酯修饰的miRNA,它能够模拟miRNA的功能来调节靶基因的表达。合成了模拟miRNA874的阿戈美拉汀874,以下调髓核(NP)中基质金属蛋白酶(MMPs)的表达。同时,通过四臂聚乙二醇 - 巯基(4 - arm PEG - SH)与银离子溶液的Ag - S配位反应合成了一种聚乙二醇(PEG)水凝胶,该水凝胶具有可注射、自愈、抗菌、可降解和高吸水性等特性,与椎间盘的机制完美匹配。通过将负载阿戈美拉汀的PEG水凝胶递送至退变的椎间盘,原位构建基因 - 水凝胶微环境,降低MMPs的表达,调节椎间盘NP中ECM的合成/分解代谢平衡,并改善组织微环境再生。