Samolyk Bryanna L, Pace Zoe Y, Li Juanyong, Billiar Kristen L, Coburn Jeannine M, Whittington Catherine F, Pins George D
Department of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.
Tissue Eng Part C Methods. 2024 May;30(5):217-228. doi: 10.1089/ten.TEC.2023.0363. Epub 2024 Apr 23.
Functional regeneration of anisotropically aligned tissues such as ligaments, microvascular networks, myocardium, or skeletal muscle requires a temporal and spatial series of biochemical and biophysical cues to direct cell functions that promote native tissue regeneration. When these cues are lost during traumatic injuries such as volumetric muscle loss (VML), scar formation occurs, limiting the regenerative capacity of the tissue. Currently, autologous tissue transfer is the gold standard for treating injuries such as VML but can result in adverse outcomes including graft failure, donor site morbidity, and excessive scarring. Tissue-engineered scaffolds composed of biomaterials, cells, or both have been investigated to promote functional tissue regeneration but are still limited by inadequate tissue ingrowth. These scaffolds should provide precisely tuned topographies and stiffnesses using proregenerative materials to encourage tissue-specific functions such as myoblast orientation, followed by aligned myotube formation and recovery of functional contraction. In this study, we describe the design and characterization of novel porous fibrin scaffolds with anisotropic microarchitectural features that recapitulate the native tissue microenvironment and offer a promising approach for regeneration of aligned tissues. We used directional freeze-casting with varied fibrin concentrations and freezing temperatures to produce scaffolds with tunable degrees of anisotropy and strut widths. Nanoindentation analyses showed that the moduli of our fibrin scaffolds varied as a function of fibrin concentration and were consistent with native skeletal muscle tissue. Quantitative morphometric analyses of myoblast cytoskeletons on scaffold microarchitectures demonstrated enhanced cell alignment as a function of microarchitectural morphology. The ability to precisely control the anisotropic features of fibrin scaffolds promises to provide a powerful tool for directing aligned tissue ingrowth and enhance functional regeneration of tissues such as skeletal muscle.
各向异性排列的组织(如韧带、微血管网络、心肌或骨骼肌)的功能再生需要一系列时空生化和生物物理信号来引导促进天然组织再生的细胞功能。当这些信号在诸如大面积肌肉损伤(VML)等创伤性损伤中丧失时,就会形成疤痕,限制组织的再生能力。目前,自体组织移植是治疗VML等损伤的金标准,但可能会导致不良后果,包括移植失败、供体部位发病和过度疤痕形成。由生物材料、细胞或两者组成的组织工程支架已被研究用于促进功能性组织再生,但仍受限于组织向内生长不足。这些支架应使用促再生材料提供精确调整的拓扑结构和硬度,以促进组织特异性功能,如成肌细胞定向,随后形成排列的肌管并恢复功能性收缩。在本研究中,我们描述了具有各向异性微结构特征的新型多孔纤维蛋白支架的设计和表征,这些特征概括了天然组织微环境,并为排列组织的再生提供了一种有前景的方法。我们使用不同纤维蛋白浓度和冷冻温度的定向冷冻铸造来制备具有可调各向异性程度和支柱宽度的支架。纳米压痕分析表明,我们的纤维蛋白支架的模量随纤维蛋白浓度而变化,并且与天然骨骼肌组织一致。对支架微结构上的成肌细胞细胞骨架进行的定量形态计量分析表明,细胞排列增强是微结构形态的函数。精确控制纤维蛋白支架各向异性特征的能力有望为引导排列组织向内生长和增强骨骼肌等组织的功能再生提供一个强大的工具。