TY - GEN
T1 - Rapid and addressable immobilization of Caenorhabditis elegans in a thermo-reversible hydrogel enabled by an optoelectric microchip
AU - Chuang, H. S.
AU - Chuang, W. Y.
N1 - Funding Information:
This study was supported by the Ministry of Science and Technology under the grant number 105-2221-E-006-090-.
PY - 2016
Y1 - 2016
N2 - Caenorhabditis elegans is an ideal model animal in genetic engineering, neural science, and developmental biology. Worm immobilization is an essential step in many operations, such as microsurgeries and fluorescent imaging, yet little has been done. To this end, an immobilization technique based on the combinative use of an optoelectric device and a thermos-reversible hydrogel, Pluronic F-127, was developed in this study. The optoelectric device was coated with a photoconductive layer, allowing local circuit channels to be rapidly switched by optical illumination. The hydrogel sandwiched in the device could reach gelation within 4 s. Notably, the gelation spot was defined by the light. The immobilized C. elegans appeared to resume its full locomotion within 3 s after the light was switched off. The technique was eventually used to assist the evaluation of senescence process of the RW1596 strain. A serial sarcomere images from the same batch of worms taken at different developmental stages showed progressive muscl e degeneration. This rapid and reversible immobilization technique provides insight to realize more worm-based applications, such as drug assays, that require long-term and constant monitoring.
AB - Caenorhabditis elegans is an ideal model animal in genetic engineering, neural science, and developmental biology. Worm immobilization is an essential step in many operations, such as microsurgeries and fluorescent imaging, yet little has been done. To this end, an immobilization technique based on the combinative use of an optoelectric device and a thermos-reversible hydrogel, Pluronic F-127, was developed in this study. The optoelectric device was coated with a photoconductive layer, allowing local circuit channels to be rapidly switched by optical illumination. The hydrogel sandwiched in the device could reach gelation within 4 s. Notably, the gelation spot was defined by the light. The immobilized C. elegans appeared to resume its full locomotion within 3 s after the light was switched off. The technique was eventually used to assist the evaluation of senescence process of the RW1596 strain. A serial sarcomere images from the same batch of worms taken at different developmental stages showed progressive muscl e degeneration. This rapid and reversible immobilization technique provides insight to realize more worm-based applications, such as drug assays, that require long-term and constant monitoring.
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M3 - Conference contribution
AN - SCOPUS:85014170164
T3 - 20th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2016
SP - 481
EP - 482
BT - 20th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2016
PB - Chemical and Biological Microsystems Society
T2 - 20th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2016
Y2 - 9 October 2016 through 13 October 2016
ER -