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Integrating light-sheet imaging with virtual reality to recapitulate developmental cardiac mechanics

机译:将光片成像与虚拟现实相结合以概括发育性心脏力学

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摘要

Currently, there is a limited ability to interactively study developmental cardiac mechanics and physiology. We therefore combined light-sheet fluorescence microscopy (LSFM) with virtual reality (VR) to provide a hybrid platform for 3D architecture and time-dependent cardiac contractile function characterization. By taking advantage of the rapid acquisition, high axial resolution, low phototoxicity, and high fidelity in 3D and 4D (3D spatial + 1D time or spectra), this VR-LSFM hybrid methodology enables interactive visualization and quantification otherwise not available by conventional methods, such as routine optical microscopes. We hereby demonstrate multiscale applicability of VR-LSFM to (a) interrogate skin fibroblasts interacting with a hyaluronic acid–based hydrogel, (b) navigate through the endocardial trabecular network during zebrafish development, and (c) localize gene therapy-mediated potassium channel expression in adult murine hearts. We further combined our batch intensity normalized segmentation algorithm with deformable image registration to interface a VR environment with imaging computation for the analysis of cardiac contraction. Thus, the VR-LSFM hybrid platform demonstrates an efficient and robust framework for creating a user-directed microenvironment in which we uncovered developmental cardiac mechanics and physiology with high spatiotemporal resolution.
机译:当前,交互式研究发育性心脏力学和生理的能力有限。因此,我们将光片荧光显微镜(LSFM)与虚拟现实(VR)相结合,为3D体系结构和随时间变化的心脏收缩功能表征提供了一个混合平台。通过利用3D和4D(3D空间+ 1D时间或光谱)的快速采集,高轴向分辨率,低光毒性和高保真度,这种VR-LSFM混合方法可实现交互式可视化和定量,而传统方法则无法提供这种方法,例如常规的光学显微镜。我们在此证明VR-LSFM对(a)询问与透明质酸基水凝胶相互作用的皮肤成纤维细胞的多尺度适用性(b)在斑马鱼发育过程中通过心内膜小梁网络导航,以及(c)定位基因治疗介导的钾通道表达在成年鼠心中。我们进一步将批次强度归一化分割算法与可变形图像配准相结合,以将VR环境与成像计算进行接口,以分析心脏收缩。因此,VR-LSFM混合平台演示了一个有效且强大的框架,可用于创建用户主导的微环境,在该环境中我们发现了具有高时空分辨率的发育性心脏力学和生理学。

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