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

再生(生物学) 脚手架 纤维蛋白 材料科学 组织工程 再生医学 天然组织 骨骼肌 限制 化学 生物物理学 生物医学工程 细胞 解剖 细胞生物学 医学 生物 生物化学 免疫学 机械工程 工程类
作者
Bryanna Lynn Samolyk,Zoe Pace,Juanyong Li,Kristen L. Billiar,Jeannine M. Coburn,Catherine F. Whittington,George D. Pins
出处
期刊:Tissue Engineering Part C-methods [Mary Ann Liebert, Inc.]
标识
DOI:10.1089/ten.tec.2023.0363
摘要

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 pro-regenerative 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 to 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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