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由于容积性肌肉损失损伤导致的肌肉细胞外基质的时间变化。

Temporal changes in the muscle extracellular matrix due to volumetric muscle loss injury.

机构信息

School of Kinesiology, University of Minnesota, Minneapolis, MN, USA.

School of Medicine, Wake Forest University, Winston-Salem, NC, USA.

出版信息

Connect Tissue Res. 2022 Mar;63(2):124-137. doi: 10.1080/03008207.2021.1886285. Epub 2021 Feb 15.

Abstract

PURPOSE/AIM: Volumetric muscle loss (VML) is a devastating orthopedic injury resulting in chronic persistent functional deficits, loss of joint range of motion, pathologic fibrotic deposition and lifelong disability. However, there is only limited mechanistic understanding of VML-induced fibrosis. Herein we examined the temporal changes in the fibrotic deposition at 3, 7, 14, 28, and 48 days post-VML injury.

MATERIALS AND METHODS

Adult male Lewis rats (n = 39) underwent a full thickness 20% (85 mg) VML injury to the tibialis anterior (TA) muscle unilaterally, the contralateral TA muscle served as the control group. All TA muscles were harvested for biochemical and histologic evaluation.

RESULTS

The ratio of collagen I/III was decreased at 3, 7, and 14 days post-VML, but significantly increased at 48 days. Decorin content followed an opposite trend, significantly increasing by day 3 before dropping to below control levels by 48 days. Histological evaluation of the defect area indicates a shift from loosely packed collagen at early time points post-VML, to a densely packed fibrotic scar by 48 days.

CONCLUSIONS

The shift from early wound healing efforts to a fibrotic scar with densely packed collagen within the skeletal muscle occurs around 21 days after VML injury through dogmatic synchronous reduction of collagen III and increase in collagen I. Thus, there appears to be an early window for therapeutic intervention to prevent pathologic fibrous tissue formation, potentially by targeting CCN2/CTGF or using decorin as a therapeutic.

摘要

目的

体积性肌肉损失(VML)是一种毁灭性的骨科损伤,导致慢性持续性功能缺陷、关节活动范围丧失、病理性纤维沉积和终身残疾。然而,人们对 VML 引起的纤维化只有有限的机制理解。在此,我们检查了 VML 损伤后 3、7、14、28 和 48 天纤维化沉积的时间变化。

材料和方法

成年雄性 Lewis 大鼠(n=39)接受单侧胫骨前肌(TA)全层 20%(~85mg)VML 损伤,对侧 TA 肌肉作为对照组。所有 TA 肌肉均用于生化和组织学评估。

结果

VML 后 3、7 和 14 天,I/III 型胶原比降低,但 48 天显著增加。核心蛋白聚糖的含量呈相反趋势,第 3 天显著增加,然后在 48 天降至低于对照水平。缺陷区的组织学评估表明,VML 后早期松散堆积的胶原逐渐转变为 48 天密集的纤维疤痕。

结论

通过胶原 III 的教条性同步减少和胶原 I 的增加,VML 损伤后约 21 天,从早期伤口愈合努力到骨骼肌内密集排列的纤维疤痕发生转变。因此,似乎存在一个早期的治疗干预窗口,以防止病理性纤维组织形成,潜在的靶点是 CCN2/CTGF 或使用核心蛋白聚糖作为治疗药物。

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