Department of Biomedical Engineering and Institute for Cell Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Proc Natl Acad Sci U S A. 2010 Jan 12;107(2):565-70. doi: 10.1073/pnas.0906504107. Epub 2009 Dec 16.
Heart tissue possesses complex structural organization on multiple scales, from macro- to nano-, but nanoscale control of cardiac function has not been extensively analyzed. Inspired by ultrastructural analysis of the native tissue, we constructed a scalable, nanotopographically controlled model of myocardium mimicking the in vivo ventricular organization. Guided by nanoscale mechanical cues provided by the underlying hydrogel, the tissue constructs displayed anisotropic action potential propagation and contractility characteristic of the native tissue. Surprisingly, cell geometry, action potential conduction velocity, and the expression of a cell-cell coupling protein were exquisitely sensitive to differences in the substratum nanoscale features of the surrounding extracellular matrix. We propose that controlling cell-material interactions on the nanoscale can stipulate structure and function on the tissue level and yield novel insights into in vivo tissue physiology, while providing materials for tissue repair.
心脏组织在多个尺度上具有复杂的结构组织,从宏观到纳米,但对心脏功能的纳米级控制尚未得到广泛分析。受天然组织超微结构分析的启发,我们构建了一种可扩展的、纳米拓扑控制的心肌模型,模拟体内心室组织。在底层水凝胶提供的纳米级机械线索的指导下,组织构建体表现出与天然组织相似的各向异性动作电位传播和收缩性。令人惊讶的是,细胞几何形状、动作电位传导速度以及细胞间连接蛋白的表达对周围细胞外基质基底纳米特征的差异非常敏感。我们提出,控制纳米级的细胞-材料相互作用可以规定组织水平的结构和功能,并为体内组织生理学提供新的见解,同时为组织修复提供材料。