间充质干细胞分泌组在慢性肌腱损伤愈合中的作用:大鼠肌腱的前胶原分析和组织病理学。

IF 1.7 Q4 CELL BIOLOGY
Stem Cells and Cloning-Advances and Applications Pub Date : 2025-04-09 eCollection Date: 2025-01-01 DOI:10.2147/SCCAA.S512079
Andi Dhedie Prasatia Sam, Warsinggih Warsinggih, Muhammad Andry Usman, Muhammad Phetrus Johan, Heri Suroto, M Ruksal Saleh, Muhammad Sakti, Andi Alfian Zainuddin, Andi Firman Mubarak
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引用次数: 0

摘要

背景:慢性肌腱损伤往往导致愈合能力下降,需要创新的治疗方法。间充质干细胞(MSCs)分泌组已成为通过旁分泌信号增强肌腱修复的有希望的选择。本研究评估了来自肌腱来源干细胞(TDSCs)和脂肪来源干细胞(ASCs)的间充质干细胞分泌组在大鼠模型中治疗慢性跟腱损伤的有效性。重点是前胶原I型n末端肽(PINP)和前胶原III型n末端肽(PIIINP)水平和组织病理学变化。方法:将14只成年雄性大鼠分为4组:ⅰ组(TDSC分泌组)、ⅱ组(ASC分泌组)、ⅲ组(TDSC与ASC分泌组联合)和ⅳ组(对照组)。通过PINP和PIIINP免疫血清学标志物评估愈合反应,并分析组织病理学变化。该研究遵循了ARRIVE和ICLAS指南,并遵循了美国国立卫生研究院(NIH)实验动物护理和使用指南。结果:联合治疗组患者的PINP水平明显高于对照组(p = 0.004),提示I型胶原合成增强。然而,各组间PIIINP水平无显著差异。组织病理学分析显示,治疗组和对照组在胶原排列或血管生成方面没有显著差异。结论:MSC分泌组,特别是tdsc与ASCs的结合,可能加速I型胶原的合成,改善肌腱的微观结构。这表明它们治疗慢性肌腱损伤的潜力。然而,进一步的研究,更长的观察期和临床试验是至关重要的,以证实这些发现,并提高我们对肌腱愈合的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mesenchymal Stem Cell Secretome Effectiveness in Healing Chronic Tendon Injury: Procollagen Analysis and Histopathology in Rat Tendons.

Background: Chronic tendon injuries often lead to diminished healing capacity, necessitating innovative treatments. Mesenchymal stem cells (MSCs) secretome has emerged as a promising option for enhancing tendon repair through paracrine signaling. This study evaluates the effectiveness of MSC secretome, derived from tendon-derived stem cells (TDSCs) and adipose-derived stem cells (ASCs) in healing chronic Achilles tendon injuries in a rat model. The focus is on Procollagen Type I N-Terminal Peptide (PINP) and Procollagen Type III N-Terminal Peptide (PIIINP) levels, and histopathological changes.

Methods: Fourteen adult male rats were divided into four groups: Group I (TDSC secretome), Group II (ASC secretome), Group III (combination of TDSC and ASC secretome), and Group IV (control). The healing response was assessed through PINP and PIIINP immunoserological markers, and histopathological changes were analyzed. The study adhered to ARRIVE and ICLAS guidelines and followed the National Institutes of Health (NIH) Guide for the Care and Use of Laboratory Animals.

Results: The combination group showed significantly higher PINP levels compared to the control group (p = 0.004), suggesting enhanced Type I collagen synthesis. However, no significant differences in PIIINP levels were observed among the groups. Histopathological analysis showed no significant differences in collagen alignment or angiogenesis between treatment and control groups.

Conclusion: The MSC secretome, particularly the combination of TDSCs and ASCs, may accelerate collagen Type I synthesis and improve tendon microstructure. This suggests their potential for treating chronic tendon injuries. However, further research with longer observation periods and clinical trials is crucial to confirm these findings and advance our understanding of tendon healing.

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来源期刊
CiteScore
6.50
自引率
0.00%
发文量
10
审稿时长
16 weeks
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