High-throughput zebrafish histology

被引:104
|
作者
Sabaliauskas, Nicole A.
Foutz, Christina A.
Mest, Jason R.
Budgeon, Lynn R.
Sidor, Adam T.
Gershenson, Joseph A.
Joshi, Sanjay B.
Cheng, Keith C. [1 ]
机构
[1] Penn State Univ, Coll Med, Dept Pathol, Jake Gittlen Canc Res Fdn, Hershey, PA 17033 USA
[2] Penn State Univ, Dept Ind & Mfg Engn, University Pk, PA 16802 USA
关键词
zebrafish; histology; high-throughput toxicology method; atlas screen; array genetic screen;
D O I
10.1016/j.ymeth.2006.03.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The morphological effects of mutation and disease are often critical to our understanding of normal and abnormal function. The power and popularity of zebrafish as a forward and reverse genetic vertebrate model system, combined with its small size, have made it an ideal model in which to study the genetics of histologically scorable phenotypes. The presence of multiple tissue types in this organism's small larvae also makes it a potentially important model for toxicological analysis. Studying histological phenotypes is greatly enhanced by high-throughput methods of histology. Here, we describe details of high-throughput histology of the zebrafish using larval arrays, along with recent advances in mold design and discussion of work in progress that will lead to easier ways for people in the field to more rapidly score phenotypes in arrays. These detailed descriptions, together with the troubleshooting guide, should enable any laboratory with ties to a histology facility to perform high-throughput histology of zebrafish. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:246 / 254
页数:9
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