通过透明质酸水凝胶系统递送氰苷a诱导的间充质干细胞增强软骨形成潜能和骨关节炎治疗。

IF 7 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Xingyan An, Qirong Zhou, Shihao Sheng, Anfu Deng, Han Liu, Xiuhui Wang, Qin Zhang, Yingying Jing, Ke Xu, Chongru He, Robert Chunhua Zhao, Jiacan Su
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引用次数: 0

摘要

骨关节炎(OA)是一种常见的退行性关节疾病,严重影响老年人的生活质量。中药,特别是药草根及其有效成分氰皂苷A (CyA),已被用于治疗OA,通过促进软骨细胞增殖,抑制炎症因子,维持关节稳态。同时,来自胎盘脐带、骨髓和脂肪组织的间充质干细胞(MSC)因其软骨分化能力在OA治疗中的潜力而受到关注。本研究探讨了CyA和MSC在促进软骨再生方面的治疗协同作用。用0.5 mg/mL CyA处理MSC 3天后,可获得最佳软骨分化,显著增加关键软骨特异性基因ACAN、COL2A和SOX9的表达。比较基因表达和通路分析显示,cya诱导的MSC (C-MSC)调节关键信号通路,包括TGF-β、PI3K-Akt和Wnt,显示其在软骨修复中的潜力。此外,在il -1β处理的人软骨细胞中,与msc来源的外泌体相比,c - msc来源的外泌体表现出更好的抗炎和抗凋亡作用,增强了成软骨基因的表达,减少了软骨的降解。为了实现靶向递送,使用甲基丙烯酸透明质酸(HAMA)开发了一种新型可注射水凝胶系统(HAMA@C-MSC)。这种水凝胶促进细胞均匀分布,保持结构完整性,并表现出良好的生物相容性和生物安全性,无细胞毒性或溶血作用。使用大鼠内侧半月板OA模型的体内研究证实HAMA@C-MSC显著改善软骨结构,增强软骨细胞再生,恢复胶原完整性,优于其他治疗组,通过影像学、组织学和分子分析验证了这一点。这些发现强调HAMA@C-MSC作为OA的一种有前景的治疗策略,利用C-MSC和先进的水凝胶技术的协同作用来实现增强软骨再生和关节保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced Chondrogenic Potential and Osteoarthritis Treatment Using Cyaonoside A-Induced MSC Delivered via a Hyaluronic Acid-Based Hydrogel System.

Osteoarthritis (OA) is a prevalent degenerative joint disease that significantly impacts the quality of life in the elderly. Traditional Chinese medicine, particularly Medicinal Cyathula Root and its active component Cyaonoside A (CyA), has been utilized to treat OA by promoting chondrocyte proliferation, inhibiting inflammatory factors, and maintaining joint homeostasis. Concurrently, mesenchymal stem cells (MSC) derived from placental umbilical cord, bone marrow, and adipose tissue have gained attention for their potential in OA treatment due to their chondrogenic differentiation capabilities. This study explored the therapeutic synergy of CyA and MSC for enhanced cartilage regeneration. Optimal chondrogenic differentiation was achieved by treating MSC with 0.5 mg/mL CyA for 3 days, significantly increasing the expression of key cartilage-specific genes ACAN, COL2A, and SOX9. Comparative gene expression and pathway analyses revealed that CyA-induced MSC (C-MSC) modulate critical signaling pathways, including TGF-β, PI3K-Akt, and Wnt, demonstrating their potential in cartilage repair. Furthermore, C-MSC-derived exosomes exhibited superior anti-inflammatory and anti-apoptotic effects compared to MSC-derived exosomes in IL-1β-treated human chondrocytes, enhancing chondrogenic gene expression and reducing cartilage degradation. To enable targeted delivery, a novel injectable hydrogel system (HAMA@C-MSC) was developed using methylacrylated hyaluronic acid (HAMA). This hydrogel facilitated uniform cell distribution, maintained structural integrity, and demonstrated excellent biocompatibility and biosafety, with no cytotoxic or hemolytic effects. In vivo studies using a rat destabilization of the medial meniscus OA model confirmed that HAMA@C-MSC significantly improved cartilage structure, enhanced chondrocyte regeneration, and restored collagen integrity, outperforming other treatment groups as validated through imaging, histology, and molecular analyses. These findings highlight HAMA@C-MSC as a promising therapeutic strategy for OA, leveraging the synergistic effects of C-MSC and advanced hydrogel technology to achieve enhanced cartilage regeneration and joint protection.

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来源期刊
Aging and Disease
Aging and Disease GERIATRICS & GERONTOLOGY-
CiteScore
14.60
自引率
2.70%
发文量
138
审稿时长
10 weeks
期刊介绍: Aging & Disease (A&D) is an open-access online journal dedicated to publishing groundbreaking research on the biology of aging, the pathophysiology of age-related diseases, and innovative therapies for conditions affecting the elderly. The scope encompasses various diseases such as Stroke, Alzheimer's disease, Parkinson’s disease, Epilepsy, Dementia, Depression, Cardiovascular Disease, Cancer, Arthritis, Cataract, Osteoporosis, Diabetes, and Hypertension. The journal welcomes studies involving animal models as well as human tissues or cells.
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