TY - JOUR
T1 - Visualizing and quantifying molecular and cellular processes in Caenorhabditis elegans using light microscopy
AU - Shah, Pavak
AU - Bao, Zhirong
AU - Zaidel-Bar, Ronen
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Oxford University Press on behalf of Genetics Society of America. All rights reserved.
PY - 2022/8
Y1 - 2022/8
N2 - Light microscopes are the cell and developmental biologists' "best friend,"providing a means to see structures and follow dynamics from the protein to the organism level. A huge advantage of Caenorhabditis elegans as a model organism is its transparency, which coupled with its small size means that nearly every biological process can be observed and measured with the appropriate probe and light microscope. Continuous improvement in microscope technologies along with novel genome editing techniques to create transgenic probes have facilitated the development and implementation of a dizzying array of methods for imaging worm embryos, larvae, and adults. In this review, we provide an overview of the molecular and cellular processes that can be visualized in living worms using light microscopy. A partial inventory of fluorescent probes and techniques successfully used in worms to image the dynamics of cells, organelles, DNA, and protein localization and activity is followed by a practical guide to choosing between various imaging modalities, including widefield, confocal, lightsheet, and structured illumination microscopy. Finally, we discuss the available tools and approaches, including machine learning, for quantitative image analysis tasks, such as colocalization, segmentation, object tracking, and lineage tracing. Hopefully, this review will inspire worm researchers who have not yet imaged their worms to begin, and push those who are imaging to go faster, finer, and longer.
AB - Light microscopes are the cell and developmental biologists' "best friend,"providing a means to see structures and follow dynamics from the protein to the organism level. A huge advantage of Caenorhabditis elegans as a model organism is its transparency, which coupled with its small size means that nearly every biological process can be observed and measured with the appropriate probe and light microscope. Continuous improvement in microscope technologies along with novel genome editing techniques to create transgenic probes have facilitated the development and implementation of a dizzying array of methods for imaging worm embryos, larvae, and adults. In this review, we provide an overview of the molecular and cellular processes that can be visualized in living worms using light microscopy. A partial inventory of fluorescent probes and techniques successfully used in worms to image the dynamics of cells, organelles, DNA, and protein localization and activity is followed by a practical guide to choosing between various imaging modalities, including widefield, confocal, lightsheet, and structured illumination microscopy. Finally, we discuss the available tools and approaches, including machine learning, for quantitative image analysis tasks, such as colocalization, segmentation, object tracking, and lineage tracing. Hopefully, this review will inspire worm researchers who have not yet imaged their worms to begin, and push those who are imaging to go faster, finer, and longer.
KW - WormBook
KW - activity sensors
KW - confocal microscopy
KW - fluorescence microscopy
KW - green fluorescent protein
KW - image analysis
KW - lightsheet microscopy
KW - localization
KW - molecular dynamics
KW - spatiotemporal resolution
KW - super resolution
UR - http://www.scopus.com/inward/record.url?scp=85135421363&partnerID=8YFLogxK
U2 - 10.1093/genetics/iyac068
DO - 10.1093/genetics/iyac068
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C2 - 35766819
AN - SCOPUS:85135421363
SN - 0016-6731
VL - 221
JO - Genetics
JF - Genetics
IS - 4
M1 - iyac068
ER -