Scholarlink

Background: <p>Osteoarthritis (OA), a widespread chronic joint disorder mainly affecting the elderly, currently lacks a definitive cure. This study investigated the efficacy of exosomes (Exos) extracted from human umbilical cord MSCs (hucMSCs) in the treatment of OA, and preliminarily explored the mechanisms.</p> Methods: <p>A rat osteoarthritis model was constructed by surgical induction. The cartilage morphology was observed after pathological staining; expression of cartilage matrix protein, autophagy-related protein and β-catenin were detected by immunohistochemistry; and inflammatory factors in serum were tested by ELISA. In cellular experiments, human primary chondrocytes were induced with IL-1β to build the OA microenvironment. The levels of relevant proteins in each group were analyzed.</p> Results: <p>Comparing to the OA model, the Exos treatment showed positive effects in reducing OARSI score and Mankin score, decreasing joint space stenosis, promoting matrix synthesis, increasing autophagy, and decreasing β-catenin. The results of the cellular experiments were consistent with those from the animal experiments. However, the Wnt/β-catenin pathway was greatly activated, the levels of matrix proteins and autophagy were distinctly reduced in the Exos + LiCl group comparing to the exosome-treated group.</p> Conclusion: <p>hucMSCs-Exos effectively attenuated the pathological damage of OA cartilage and chondrocytes, promoted the synthesis of cartilage matrix, reduced inflammation, suppressed the Wnt/β-catenin pathway, and enhanced autophagy which promoted the repair of OA cartilage.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Exosomes Extracted from Human Umbilical Cord MSCs Contribute to Osteoarthritic Cartilage and Chondrocytes Repair Through Enhancing Autophagy While Suppressing the Wnt/β-Catenin Pathway

  • 期刊论文

  • 发表日期：

    2025年4月15日

查看全文
  • Shangzhu Qin,
  • Aijie Zhang,
  • Lian Duan,
  • Fang Lin,
  • Mingcai Zhao

摘要

Background:

Osteoarthritis (OA), a widespread chronic joint disorder mainly affecting the elderly, currently lacks a definitive cure. This study investigated the efficacy of exosomes (Exos) extracted from human umbilical cord MSCs (hucMSCs) in the treatment of OA, and preliminarily explored the mechanisms.

Methods:

A rat osteoarthritis model was constructed by surgical induction. The cartilage morphology was observed after pathological staining; expression of cartilage matrix protein, autophagy-related protein and β-catenin were detected by immunohistochemistry; and inflammatory factors in serum were tested by ELISA. In cellular experiments, human primary chondrocytes were induced with IL-1β to build the OA microenvironment. The levels of relevant proteins in each group were analyzed.

Results:

Comparing to the OA model, the Exos treatment showed positive effects in reducing OARSI score and Mankin score, decreasing joint space stenosis, promoting matrix synthesis, increasing autophagy, and decreasing β-catenin. The results of the cellular experiments were consistent with those from the animal experiments. However, the Wnt/β-catenin pathway was greatly activated, the levels of matrix proteins and autophagy were distinctly reduced in the Exos + LiCl group comparing to the exosome-treated group.

Conclusion:

hucMSCs-Exos effectively attenuated the pathological damage of OA cartilage and chondrocytes, promoted the synthesis of cartilage matrix, reduced inflammation, suppressed the Wnt/β-catenin pathway, and enhanced autophagy which promoted the repair of OA cartilage.