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A stylized image of a nematode worm (C. elegans) adult encircled by embryos. Credit: Yicong Wu |
The beauty of live-imaging studies is that the specimen is alive, allowing dynamics such as cell division and embryonic development to be recorded over time.
Yet the frustration of live-imaging studies is the specimen is alive – wriggling, twisting, escaping the field of view. Plus, it’s delicate, susceptible to heat damage or death from the imaging equipment itself.
A technical solution to this quandary recently emerged from the MBL Embryology course, in “a classic example of the collaborative effort here at MBL,” says MBL Imaging Research Specialist Carsten Wolff.
“During the 2021 Embryology course, we started to develop a technique that enables us to image adult C. elegans worms for longer periods of time, and at high resolution, using light sheet microscopy,” says Wolff. A group of course faculty and staff, collaborating with MBL imagers, fine-tuned the protocol during the 2022 course and wrote up the paper, which is published this month in Frontiers in Cell and Developmental Biology.
The nematode C. elegans is a popular organism in biological and biomedical research. Light-sheet fluorescence microscopy (LSFM) has been very successful in capturing embryonic processes in C. elegans, as well as in mice and zebrafish. But once the organisms hatch out, LSFM presents limitations.