纤维蛋白
生物加工
材料科学
心肌细胞
生物医学工程
组织工程
细胞外基质
骨骼肌
体内
刚度
肌肉组织
细胞生物学
机械转化
生物物理学
基质(化学分析)
肌原纤维
纳米技术
再生医学
解剖
天然组织
伤口愈合
脚手架
剪切(地质)
组织修复
间充质干细胞
血管平滑肌
肌肉僵硬
平滑肌
血管生成
作者
Su Hyun Jung,김민준,Da‐Yoon Kim,Min Kyu Kim,Sieun Lee,Yoonhee Jin,Joo H. Kang
标识
DOI:10.1002/adma.202523542
摘要
Volumetric muscle loss (VML), a severe injury involving irreversible loss of both muscle tissue and vasculature, poses a major barrier to the development of clinically viable muscle grafts. Functional restoration requires engineered constructs capable of reconstructing both contractile and vascular components that can functionally integrate with the host vasculature. Here, we introduce SPARC (spatio-chimeric, plasma-based, anisotropic, and shear-responsive construct), a mechanically bimodal fibrin hydrogel engineered via shear-guided assembly of plasma fibrin to recreate the structural and mechanical heterogeneity of native muscle. Controlled microfluidic shear generates aligned fibrillar bundles and a spatially graded bimodal stiffness architecture, establishing stiff, bundle-dense regions that favor myogenic differentiation and compliant regions that promote endothelial morphogenesis. When co-cultured with myoblasts and endothelial cells, the resulting anisotropic matrix directs spatially organized myogenic maturation and endothelial morphogenesis. In vivo evaluation in a murine VML model shows that vascularized muscle SPARC grafts restore muscle architecture and function, promoting neovascularization, myofiber regeneration, and enhanced motor recovery. Through its spatially mechano-programmed design, SPARC enables coordinated myogenic and endothelial organization within a single construct, establishing a scalable biofabrication strategy for functional repair of extensive muscle defects.
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