Multi-sample SPIM image acquisition, processing and analysis of vascular growth in zebrafish

被引:31
|
作者
Daetwyler, Stephan [1 ,2 ,3 ]
Guenther, Ulrik [1 ,3 ,4 ]
Modes, Carl D. [1 ,3 ]
Harrington, Kyle [5 ]
Huisken, Jan [1 ,6 ,7 ]
机构
[1] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[2] UT Southwestern Med Ctr, Dept Cell Biol, Dallas, TX 75390 USA
[3] Ctr Syst Biol Dresden, D-01307 Dresden, Germany
[4] Tech Univ Dresden, Chair Sci Comp Syst Biol, Fac Comp Sci, D-01069 Dresden, Germany
[5] Univ Idaho, Virtual Technol & Design, Moscow, ID 83844 USA
[6] Morgridge Inst Res, Madison, WI 53715 USA
[7] Univ Wisconsin, Dept Integrat Biol, Madison, WI 53706 USA
来源
DEVELOPMENT | 2019年 / 146卷 / 06期
关键词
Multi-sample imaging; Light sheet microscopy; Zebrafish; SPIM; Vasculature; Segmentation; Growth models; FLUORESCENCE MICROSCOPY; LIGHT; TRANSPLANTATION; PLATFORM; MODEL;
D O I
10.1242/dev.173757
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To quantitatively understand biological processes that occur over many hours or days, it is desirable to image multiple samples simultaneously, and automatically process and analyse the resulting datasets. Here, we present a complete multi-sample preparation, imaging, processing and analysis workflow to determine the development of the vascular volume in zebrafish. Up to five live embryos were mounted and imaged simultaneously over several days using selective plane illumination microscopy (SPIM). The resulting large imagery dataset of several terabytes was processed in an automated manner on a high-performance computer cluster and segmented using a novel segmentation approach that uses images of red blood cells as training data. This analysis yielded a precise quantification of growth characteristics of the whole vascular network, head vasculature and tail vasculature over development. Our multi-sample platform demonstrates effective upgrades to conventional single-sample imaging platforms and paves the way for diverse quantitative long-term imaging studies.
引用
收藏
页数:10
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