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自组装肽水凝胶在前交叉韧带重建小鼠模型中的修复潜力

Repair potential of self-assembling peptide hydrogel in a mouse model of anterior cruciate ligament reconstruction.

作者信息

Fujino Keitaro, Yamamoto Natsuki, Yoshimura Yukiko, Yokota Atsushi, Hirano Yoshiaki, Neo Masashi

机构信息

Department of Orthopedic Surgery Osaka Medical and Pharmaceutical University Osaka Japan.

Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials, and Bioengineering Kansai University Osaka Japan.

出版信息

J Exp Orthop. 2024 Jun 19;11(3):e12061. doi: 10.1002/jeo2.12061. eCollection 2024 Jul.

Abstract

PURPOSE

Establishing zonal tendon-to-bone attachment could accelerate the anterior cruciate ligament reconstruction (ACLR) rehabilitation schedule and facilitate an earlier return to sports. KI24RGDS is a self-assembling peptide hydrogel scaffold (SAPS) with the RGDS amino acid sequence. This study aimed to elucidate the therapeutic potential of KI24RGDS in facilitating zonal tendon-to-bone attachment after ACLR.

METHODS

Sixty-four C57BL/6 mice were divided into the ACLR + SAPS and ACLR groups. ACLR was performed using the tail tendon. To assess the maturation of tendon-to-bone attachment, we quantified the area of mineralized fibrocartilage (MFC) in the tendon graft with demeclocycline. Immunofluorescence staining of α-smooth muscle actin (α-SMA) was performed to evaluate progenitor cell proliferation. The strength of tendon-to-bone attachment was evaluated using a pull-out test.

RESULTS

The MFC and maximum failure load in the ACLR + SAPS group were remarkably higher than in the ACLR group on Day 14. However, no significant difference was observed between the two groups on Day 28. The number of α-SMA-positive cells in the tendon graft was highest on Day 7 after ACLR in both the groups and was significantly higher in the ACLR + SAPS group than in the ACLR group.

CONCLUSION

This study highlighted the latent healing potential of KI24RGDS in facilitating early-stage zonal attachment of tendon grafts and bone tunnels post-ACLR. These findings may expedite rehabilitation protocols and shorten the timeline for returning to sports.

LEVEL OF EVIDENCE

Not applicable.

摘要

目的

建立区域腱骨附着可加速前交叉韧带重建(ACLR)的康复进程,并有助于更早恢复运动。KI24RGDS是一种具有RGDS氨基酸序列的自组装肽水凝胶支架(SAPS)。本研究旨在阐明KI24RGDS在促进ACLR后区域腱骨附着方面的治疗潜力。

方法

将64只C57BL/6小鼠分为ACLR + SAPS组和ACLR组。采用尾腱进行ACLR。为评估腱骨附着的成熟情况,我们用去甲金霉素对肌腱移植物中矿化纤维软骨(MFC)的面积进行定量。进行α-平滑肌肌动蛋白(α-SMA)的免疫荧光染色以评估祖细胞增殖。使用拔出试验评估腱骨附着的强度。

结果

在第14天,ACLR + SAPS组的MFC和最大破坏载荷显著高于ACLR组。然而,在第28天两组之间未观察到显著差异。两组中,肌腱移植物中α-SMA阳性细胞的数量在ACLR后第7天最高,且ACLR + SAPS组显著高于ACLR组。

结论

本研究突出了KI24RGDS在促进ACLR后肌腱移植物与骨隧道早期区域附着方面的潜在愈合潜力。这些发现可能会加快康复方案并缩短恢复运动的时间线。

证据水平

不适用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a5a/11185946/18c2b33ad335/JEO2-11-e12061-g001.jpg

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