营养不良小鼠膈肌的细胞外基质占其被动僵硬的大部分,并抵抗胶原酶消化

Q1 Medicine Matrix Biology Plus Pub Date : 2023-06-01 DOI:10.1016/j.mbplus.2023.100131
Ross P. Wohlgemuth , Ryan M. Feitzinger , Kyle E. Henricson , Daryl T. Dinh , Sarah E. Brashear , Lucas R. Smith
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引用次数: 1

摘要

健康的骨骼肌细胞外基质(ECM)具有多种功能,包括为肌纤维提供结构完整性,实现侧向力传递,并有助于整体被动机械性能。在杜兴肌营养不良等疾病中,ECM物质(主要是胶原蛋白)积聚,导致纤维化。先前的研究表明,纤维化肌肉通常比健康肌肉更硬,部分原因是ECM内胶原纤维的数量增加和结构改变。这意味着纤维化基质比健康基质更硬。然而,尽管之前的研究试图量化细胞外对肌肉被动僵硬的贡献,但结果取决于所用方法的类型。因此,本研究的目的是比较健康和纤维化肌肉ECM的硬度,并证明两种方法量化肌肉中基于细胞外的硬度的有效性,即脱细胞和胶原酶消化。这些方法已被证明可以分别去除肌肉纤维或消融胶原纤维的完整性,同时保持细胞外基质的含量。将这些方法与对野生型和D2.mdx小鼠的机械测试结合使用,我们发现隔膜中的大多数被动硬度依赖于ECM,并且D2.mdx隔膜ECM对细菌胶原酶的消化具有抵抗力。我们认为这种阻力是由于D2.mdx隔膜ECM中胶原交联和胶原堆积密度增加所致。总之,虽然我们没有发现纤维化ECM的硬度增加,但我们确实观察到D2.mdx隔膜传递了对胶原酶消化的抵抗力。这些发现表明,测量基于ECM的刚度的不同方法各有其局限性,并可能产生不同的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The extracellular matrix of dystrophic mouse diaphragm accounts for the majority of its passive stiffness and is resistant to collagenase digestion

The healthy skeletal muscle extracellular matrix (ECM) has several functions including providing structural integrity to myofibers, enabling lateral force transmission, and contributing to overall passive mechanical properties. In diseases such as Duchenne Muscular dystrophy, there is accumulation of ECM materials, primarily collagen, which results in fibrosis. Previous studies have shown that fibrotic muscle is often stiffer than healthy muscle, in part due to the increased number and altered architecture of collagen fibers within the ECM. This would imply that the fibrotic matrix is stiffer than the healthy matrix. However, while previous studies have attempted to quantify the extracellular contribution to passive stiffness in muscle, the outcomes are dependent on the type of method used. Thus, the goals of this study were to compare the stiffness of healthy and fibrotic muscle ECM and to demonstrate the efficacy of two methods for quantifying extracellular-based stiffness in muscle, namely decellularization and collagenase digestion. These methods have been demonstrated to remove the muscle fibers or ablate collagen fiber integrity, respectively, while maintaining the contents of the extracellular matrix. Using these methods in conjunction with mechanical testing on wildtype and D2.mdx mice, we found that a majority of passive stiffness in the diaphragm is dependent on the ECM, and the D2.mdx diaphragm ECM is resistant to digestion by bacterial collagenase. We propose that this resistance is due to the increased collagen cross-links and collagen packing density in the ECM of the D2.mdx diaphragm. Taken altogether, while we did not find increased stiffness of the fibrotic ECM, we did observe that the D2.mdx diaphragm conveyed resistance against collagenase digestion. These findings demonstrate how different methods for measuring ECM-based stiffness each have their own limitations and can produce different results.

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来源期刊
Matrix Biology Plus
Matrix Biology Plus Medicine-Histology
CiteScore
9.00
自引率
0.00%
发文量
25
审稿时长
105 days
期刊最新文献
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