4.7 Article

Preparation of EGCG decorated, injectable extracellular vesicles for cartilage repair in rat arthritis

期刊

REGENERATIVE BIOMATERIALS
卷 8, 期 6, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/rb/rbab067

关键词

cartilage repair; arthritis; tea polyphenol; extracellular vesicles

资金

  1. National Natural Science Foundation of China [82072076, 81771987, 82072165]
  2. Natural Science Foundation of Liaoning Province [201602309]

向作者/读者索取更多资源

Combining EGCG with macrophage-derived extracellular vesicles showed promising results in treating rheumatoid arthritis, reducing arthritis-related protein expression and promoting cartilage repair. Animal experiments demonstrated that this treatment significantly reduced joint swelling and repaired cartilage.
Arthritis is a kind of chronic inflammatory autoimmune disease, which can destroy joint cartilage and bone, leading to joint pain, joint swelling, and limited mobility. Traditional therapies have many side effects or focus too much on anti-inflammation while neglecting joint repair. In this experiment, we combined Epigallocatechin gallate (EGCG) with extracellular vesicles derived from macrophages to treat rheumatoid arthritis. Sustained-release resulted in a significant decrease in chondrocyte expression of hypoxia-inducible factor 1-alpha, a decrease in apoptosis-related proteins Cytochrome C, Caspase-3, Caspase-9, and Bax. Molecular biological analysis showed that extracellular vesicles-encapsulated EGCG (EVs-EGCG) more significantly upregulated type II collagen expression by about 1.8-fold than EGCG alone, which was more beneficial for arthritis repair. Animal experiments revealed that these EGCG-coated extracellular vesicles significantly reduced swelling, decreased synovial hyperplasia, repaired cartilage, and attenuated arthritis-related pathology scores in arthritic rats. Measurement data showed that EVs-EGCG treatment reduced joint swelling by approximately 39.5% in rheumatoid rats. In vitro studies have shown that this EVs-EGCG can increase the expression of cartilage type II collagen and reduce apoptosis of chondrocytes. Moreover, it was demonstrated in vivo experiments to reduce cartilage destruction in rheumatoid arthritis rats, providing a solution for the treatment of rheumatoid arthritis.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据