Developing Porous Fibrin Scaffolds with Tunable Anisotropic Features to Direct Myoblast Orientation.

IF 2.7 4区 医学 Q3 CELL & TISSUE ENGINEERING Tissue engineering. Part C, Methods Pub Date : 2024-05-01 Epub Date: 2024-04-23 DOI:10.1089/ten.TEC.2023.0363
Bryanna L Samolyk, Zoe Y Pace, Juanyong Li, Kristen L Billiar, Jeannine M Coburn, Catherine F Whittington, George D Pins
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Abstract

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.

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开发具有可调各向异性特征的多孔纤维蛋白支架,引导成肌细胞定向
韧带、微血管网、心肌或骨骼肌等各向异性排列组织的功能再生需要一系列时间和空间上的生化和生物物理线索来引导细胞功能,从而促进原生组织再生。在创伤(如体积性肌肉缺失(VML))过程中,如果失去了这些线索,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 等损伤的黄金标准,但可能导致移植失败、供体部位发病率高和瘢痕过多等不良后果。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,但仍受到组织生长不足的限制。这些支架应使用促进再生的材料提供精确调整的形貌和硬度,以促进组织的特定功能,如肌细胞定向,然后形成排列整齐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,以再现原生组织的微环境,并为排列整齐的组织再生提供一种前景广阔的方法。我们采用定向冷冻铸造技术,通过改变纤维蛋白浓度和冷冻温度,生产出各向异性程度和支柱宽度可调的支架。纳米压痕分析表明,纤维蛋白支架的模量随纤维蛋白浓度的变化而变化,与原生骨骼肌组织一致。对支架微体系结构上的成肌细胞细胞骨架进行的定量形态分析表明,细胞排列与微体系结构形态有关。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整齐的组织生长和增强骨骼肌等组织的功能再生提供强有力的工具。
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来源期刊
Tissue engineering. Part C, Methods
Tissue engineering. Part C, Methods Medicine-Medicine (miscellaneous)
CiteScore
5.10
自引率
3.30%
发文量
136
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues. Tissue Engineering Methods (Part C) presents innovative tools and assays in scaffold development, stem cells and biologically active molecules to advance the field and to support clinical translation. Part C publishes monthly.
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