Microfluidic Technologies for High Throughput Screening Through Sorting and On-Chip Culture of C. elegans

被引:25
|
作者
Midkiff, Daniel [1 ]
San-Miguel, Adriana [1 ]
机构
[1] North Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
来源
MOLECULES | 2019年 / 24卷 / 23期
关键词
screening; microfluidics; phenotyping; genetics; aging; CAENORHABDITIS-ELEGANS; HIGH-RESOLUTION; NERVOUS-SYSTEM; DEVICE; BEHAVIOR; ELECTROTAXIS; OPTOGENETICS; PLATFORM; PATTERN;
D O I
10.3390/molecules24234292
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nematode Caenorhabditis elegans is a powerful model organism that has been widely used to study molecular biology, cell development, neurobiology, and aging. Despite their use for the past several decades, the conventional techniques for growth, imaging, and behavioral analysis of C. elegans can be cumbersome, and acquiring large data sets in a high-throughput manner can be challenging. Developments in microfluidic "lab-on-a-chip" technologies have improved studies of C. elegans by increasing experimental control and throughput. Microfluidic features such as on-chip control layers, immobilization channels, and chamber arrays have been incorporated to develop increasingly complex platforms that make experimental techniques more powerful. Genetic and chemical screens are performed on C. elegans to determine gene function and phenotypic outcomes of perturbations, to test the effect that chemicals have on health and behavior, and to find drug candidates. In this review, we will discuss microfluidic technologies that have been used to increase the throughput of genetic and chemical screens in C. elegans. We will discuss screens for neurobiology, aging, development, behavior, and many other biological processes. We will also discuss robotic technologies that assist in microfluidic screens, as well as alternate platforms that perform functions similar to microfluidics.
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页数:31
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