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Long-termC. elegansimmobilization enables high resolution developmental studiesin vivo
Author(s) -
Simon Berger,
Evelyn Lattmann,
Tinri AegerterWilmsen,
Michael O. Hengartner,
Alex Hajnal,
Andrew J. deMello,
Xavier Casadevall i Solvas
Publication year - 2018
Publication title -
lab on a chip
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.064
H-Index - 210
eISSN - 1473-0197
pISSN - 1473-0189
DOI - 10.1039/c7lc01185g
Subject(s) - term (time) , in vivo , biology , resolution (logic) , computational biology , computer science , physics , genetics , artificial intelligence , quantum mechanics
Live-imaging of C. elegans is essential for the study of conserved cellular pathways (e.g. EGFR/Wnt signaling) and morphogenesis in vivo. However, the usefulness of live imaging as a research tool has been severely limited by the need to immobilize worms prior to and during imaging. Conventionally, immobilization is achieved by employing both physical and chemical interventions. These are known to significantly affect many physiological processes, and thus limit our understanding of dynamic developmental processes. Herein we present a novel, easy-to-use microfluidic platform for the long-term immobilization of viable, normally developing C. elegans, compatible with image acquisition at high resolution, thereby overcoming the limitations associated with conventional worm immobilization. The capabilities of the platform are demonstrated through the continuous assessment of anchor cell (AC) invasion and distal tip cell (DTC) migration in larval C. elegans and germ cell apoptosis in adult C. elegans in vivo for the first time.

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