4D Light-sheet imaging and interactive analysis of cardiac contractility in zebrafish larvae

被引:3
|
作者
Zhang, Xinyuan [1 ]
Almasian, Milad [1 ]
Hassan, Sohail S. S. [1 ]
Jotheesh, Rosemary [1 ]
Kadam, Vinay A. A. [1 ]
Polk, Austin R. R. [2 ]
Saberigarakani, Alireza [1 ]
Rahat, Aayan [1 ]
Yuan, Jie [1 ]
Lee, Juhyun [3 ]
Carroll, Kelli [4 ]
Ding, Yichen [1 ,5 ,6 ]
机构
[1] Univ Texas Dallas, Erik Jonsson Sch Engn & Comp Sci, Dept Bioengn, Richardson, TX 75080 USA
[2] Univ Texas Dallas, Erik Jonsson Sch Engn & Comp Sci, Dept Comp Sci, Richardson, TX 75080 USA
[3] Univ Texas Arlington, Dept Bioengn, Arlington, TX 76019 USA
[4] Austin Coll, Dept Biol, Sherman, TX 75090 USA
[5] Univ Texas Dallas, Ctr Imaging & Surg Innovat, Richardson, TX 75080 USA
[6] UT Southwestern Med Ctr, Hamon Ctr Regenerat Sci & Med, Dallas, TX 75390 USA
关键词
MICROSCOPY;
D O I
10.1063/5.0153214
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Despite ongoing efforts in cardiovascular research, the acquisition of high-resolution and high-speed images for the purpose of assessing cardiac contraction remains challenging. Light-sheet fluorescence microscopy (LSFM) offers superior spatiotemporal resolution and minimal photodamage, providing an indispensable opportunity for the in vivo study of cardiac micro-structure and contractile function in zebrafish larvae. To track the myocardial architecture and contractility, we have developed an imaging strategy ranging from LSFM system construction, retrospective synchronization, single cell tracking, to user-directed virtual reality (VR) analysis. Our system enables the four-dimensional (4D) investigation of individual cardiomyocytes across the entire atrium and ventricle during multiple cardiac cycles in a zebrafish larva at the cellular resolution. To enhance the throughput of our model reconstruction and assessment, we have developed a parallel computing-assisted algorithm for 4D synchronization, resulting in a nearly tenfold enhancement of reconstruction efficiency. The machine learning-based nuclei segmentation and VR-based interaction further allow us to quantify cellular dynamics in the myocardium from end-systole to end-diastole. Collectively, our strategy facilitates noninvasive cardiac imaging and user-directed data interpretation with improved efficiency and accuracy, holding great promise to characterize functional changes and regional mechanics at the single cell level during cardiac development and regeneration.
引用
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页数:12
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