Injectable hydrogel encapsulating siMMP13 with anti-ROS and anti-apoptotic functions for osteoarthritis treatment.

IF 10.6 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of Nanobiotechnology Pub Date : 2024-08-02 DOI:10.1186/s12951-024-02740-w
Zhongyin Ji, Xiaobin Ren, Jiayan Jin, Xin Ye, Hao Yu, Wenhan Fang, Hui Li, Yihao Zhao, Siyue Tao, Xiangxi Kong, Jiao Cheng, Zhi Shan, Jian Chen, Qingqing Yao, Fengdong Zhao, Junhui Liu
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Abstract

Background: Osteoarthritis (OA) is a degenerative joint disease characterized by the progressive degeneration of articular cartilage, leading to pain, stiffness, and loss of joint function. The pathogenesis of OA involves multiple factors, including increased intracellular reactive oxygen species (ROS), enhanced chondrocyte apoptosis, and disturbances in cartilage matrix metabolism. These processes contribute to the breakdown of the extracellular matrix (ECM) and the loss of cartilage integrity, ultimately resulting in joint damage and dysfunction. RNA interference (RNAi) therapy has emerged as a promising approach for the treatment of various diseases, including hATTR and acute hepatic porphyria. By harnessing the natural cellular machinery for gene silencing, RNAi allows for the specific inhibition of target genes involved in disease pathogenesis. In the context of OA, targeting key molecules such as matrix metalloproteinase-13 (MMP13), which plays a critical role in cartilage degradation, holds great therapeutic potential.

Results: In this study, we developed an innovative therapeutic approach for OA using a combination of liposome-encapsulated siMMP13 and NG-Monomethyl-L-arginine Acetate (L-NMMA) to form an injectable hydrogel. The hydrogel served as a delivery vehicle for the siMMP13, allowing for sustained release and targeted delivery to the affected joint. Experiments conducted on destabilization of the medial meniscus (DMM) model mice demonstrated the therapeutic efficacy of this composite hydrogel. Treatment with the hydrogel significantly inhibited the degradation of cartilage matrix, as evidenced by histological analysis showing preserved cartilage structure and reduced loss of proteoglycans. Moreover, the hydrogel effectively suppressed intracellular ROS accumulation in chondrocytes, indicating its anti-oxidative properties. Furthermore, it attenuated chondrocyte apoptosis, as demonstrated by decreased levels of apoptotic markers.

Conclusion: In summary, the injectable hydrogel containing siMMP13, endowed with anti-ROS and anti-apoptotic properties, may represent an effective therapeutic strategy for osteoarthritis in the future.

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将具有抗 ROS 和抗凋亡功能的 siMMP13 包裹在可注射的水凝胶中,用于骨关节炎的治疗。
背景:骨关节炎(OA)是一种退行性关节疾病,其特点是关节软骨逐渐退化,导致疼痛、僵硬和关节功能丧失。OA 的发病机制涉及多种因素,包括细胞内活性氧(ROS)增加、软骨细胞凋亡增强以及软骨基质代谢紊乱。这些过程导致细胞外基质(ECM)的破坏和软骨完整性的丧失,最终导致关节损伤和功能障碍。RNA 干扰(RNAi)疗法已成为治疗各种疾病(包括 hATTR 和急性肝卟啉症)的一种很有前景的方法。通过利用基因沉默的天然细胞机制,RNAi 可以特异性地抑制涉及疾病发病机制的目标基因。就 OA 而言,靶向基质金属蛋白酶-13(MMP13)等关键分子具有巨大的治疗潜力:在这项研究中,我们开发了一种创新的治疗 OA 的方法,将脂质体包裹的 siMMP13 与 NG-甲基-L-精氨酸醋酸盐(L-NMMA)结合形成一种可注射的水凝胶。水凝胶是 siMMP13 的输送载体,可持续释放并定向输送到受影响的关节。在内侧半月板不稳定(DMM)模型小鼠身上进行的实验证明了这种复合水凝胶的疗效。组织学分析表明,使用该水凝胶治疗可明显抑制软骨基质的降解,软骨结构得以保留,蛋白多糖的损失也有所减少。此外,水凝胶还能有效抑制软骨细胞内 ROS 的积累,表明其具有抗氧化特性。此外,水凝胶还能减轻软骨细胞的凋亡,凋亡标志物水平的降低就证明了这一点:总之,含有 siMMP13 的可注射水凝胶具有抗 ROS 和抗凋亡的特性,可能是未来骨关节炎的一种有效治疗策略。
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来源期刊
Journal of Nanobiotechnology
Journal of Nanobiotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
13.90
自引率
4.90%
发文量
493
审稿时长
16 weeks
期刊介绍: Journal of Nanobiotechnology is an open access peer-reviewed journal communicating scientific and technological advances in the fields of medicine and biology, with an emphasis in their interface with nanoscale sciences. The journal provides biomedical scientists and the international biotechnology business community with the latest developments in the growing field of Nanobiotechnology.
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