Tissue Engineering Lab, Department of Development and Regeneration, KU Leuven, Kortrijk, Belgium.
Univ. Lille, CNRS, Centrale Lille, UMR 9013-LaMcube-Laboratoire de Mécanique, Multiphysique, Multi-échelle, Lille, France.
Biofabrication. 2024 Mar 15;16(2). doi: 10.1088/1758-5090/ad2c99.
Decellularized matrices are an attractive choice of scaffold in regenerative medicine as they can provide the necessary extracellular matrix (ECM) components, signals and mechanical properties. Various detergent-based protocols have already been proposed for decellularization of skeletal muscle tissue. However, a proper comparison is difficult due to differences in species, muscle origin and sample sizes. Moreover, a thorough evaluation of the remaining acellular matrix is often lacking. We compared an in-house developed decellularization protocol to four previously published methods in a standardized manner. Porcine skeletal muscle samples with uniform thickness were subjected to in-depth histological, ultrastructural, biochemical and biomechanical analysis. In addition, 2D and three-dimensional cytocompatibility experiments were performed. We found that the decellularization methods had a differential effect on the properties of the resulting acellular matrices. Sodium deoxycholate combined with deoxyribonuclease I was not an effective method for decellularizing thick skeletal muscle tissue. Triton X-100 in combination with trypsin, on the other hand, removed nuclear material but not cytoplasmic proteins at low concentrations. Moreover, it led to significant alterations in the biomechanical properties. Finally, sodium dodecyl sulphate (SDS) seemed most promising, resulting in a drastic decrease in DNA content without major effects on the ECM composition and biomechanical properties. Moreover, cell attachment and metabolic activity were also found to be the highest on samples decellularized with SDS. Through a newly proposed standardized analysis, we provide a comprehensive understanding of the impact of different decellularizing agents on the structure and composition of skeletal muscle. Evaluation of nuclear content as well as ECM composition, biomechanical properties and cell growth are important parameters to assess. SDS comes forward as a detergent with the best balance between all measured parameters and holds the most promise for decellularization of skeletal muscle tissue.
去细胞基质是再生医学中一种有吸引力的支架选择,因为它们可以提供必要的细胞外基质 (ECM) 成分、信号和机械性能。已经提出了各种基于去污剂的方案来对骨骼肌组织进行去细胞化。然而,由于物种、肌肉起源和样本大小的差异,很难进行适当的比较。此外,通常缺乏对剩余去细胞基质的彻底评估。我们以标准化的方式将内部开发的去细胞化方案与之前发表的四种方法进行了比较。具有均匀厚度的猪骨骼肌样本进行了深入的组织学、超微结构、生化和生物力学分析。此外,还进行了 2D 和三维细胞相容性实验。我们发现,去细胞化方法对所得去细胞基质的性质有不同的影响。脱氧胆酸钠与脱氧核糖核酸酶 I 结合不是一种有效的方法来去除厚的骨骼肌组织。另一方面,低浓度的 Triton X-100 与胰蛋白酶结合可去除核材料,但不能去除细胞质蛋白。此外,它导致生物力学性能发生显著变化。最后,十二烷基硫酸钠 (SDS) 似乎最有前途,导致 DNA 含量急剧下降,而对 ECM 组成和生物力学性能几乎没有影响。此外,还发现细胞附着和代谢活性在 SDS 去细胞化的样本中最高。通过新提出的标准化分析,我们全面了解了不同去细胞化剂对骨骼肌结构和组成的影响。评估核含量以及 ECM 组成、生物力学特性和细胞生长是评估的重要参数。SDS 作为一种去污剂,在所有测量参数之间具有最佳的平衡,并且在骨骼肌组织的去细胞化方面最有前途。