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3D 生物打印胶原蛋白以重建人类心脏的组件。

3D bioprinting of collagen to rebuild components of the human heart.

机构信息

Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.

Engineering Research Accelerator, Carnegie Mellon University, Pittsburgh, PA 15213, USA.

出版信息

Science. 2019 Aug 2;365(6452):482-487. doi: 10.1126/science.aav9051.

Abstract

Collagen is the primary component of the extracellular matrix in the human body. It has proved challenging to fabricate collagen scaffolds capable of replicating the structure and function of tissues and organs. We present a method to 3D-bioprint collagen using freeform reversible embedding of suspended hydrogels (FRESH) to engineer components of the human heart at various scales, from capillaries to the full organ. Control of pH-driven gelation provides 20-micrometer filament resolution, a porous microstructure that enables rapid cellular infiltration and microvascularization, and mechanical strength for fabrication and perfusion of multiscale vasculature and tri-leaflet valves. We found that FRESH 3D-bioprinted hearts accurately reproduce patient-specific anatomical structure as determined by micro-computed tomography. Cardiac ventricles printed with human cardiomyocytes showed synchronized contractions, directional action potential propagation, and wall thickening up to 14% during peak systole.

摘要

胶原蛋白是人体细胞外基质的主要成分。制造能够复制组织和器官结构和功能的胶原蛋白支架一直具有挑战性。我们提出了一种使用自由形式可逆嵌入悬浮水凝胶(FRESH)3D 生物打印胶原蛋白的方法,以在各种尺度上工程化人类心脏的组成部分,从小血管到整个器官。pH 驱动凝胶化的控制提供了 20 微米长丝的分辨率、允许快速细胞渗透和微血管化的多孔微结构,以及用于多尺度血管和三叶瓣制造和灌注的机械强度。我们发现,FRESH 3D 生物打印的心脏通过微计算机断层扫描准确再现了患者特定的解剖结构。用人心肌细胞打印的心脏心室显示出同步收缩、方向动作电位传播以及在峰值收缩期间高达 14%的壁增厚。

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