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Probing and manipulating embryogenesis via nanoscale thermometry and temperature control
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4624879
Author(s) Choi, Joonhee; Zhou, Hengyun; Landig, Renate; Wu, Hai-Yin; Yu, Xiaofei; Von Stetina, Stephen E.; Kucsko, Georg; Mango, Susan E.; Needleman, Daniel J.; Samuel, Aravinthan D. T.; Maurer, Peter C.; Park, Hongkun; Lukin, Mikhail D.
Author(s) at UniBasel Mango, Susan Elizabeth
Year 2020
Title Probing and manipulating embryogenesis via nanoscale thermometry and temperature control
Journal Proceedings of the National Academy of Sciences of the United States of America
Volume 117
Number 26
Pages / Article-Number 14636-14641
Keywords cell-cycle control; cell-division asymmetry; nanoscale thermometry; nitrogen-vacancy centers; quantum sensing
Mesh terms Animals; Body Temperature, physiology; Caenorhabditis elegans, embryology; Cell Division, physiology; Embryonic Development, physiology; Nanodiamonds, chemistry; Quantum Dots, chemistry; Thermometry, instrumentation, methods
Abstract Understanding the coordination of cell-division timing is one of the outstanding questions in the field of developmental biology. One active control parameter of the cell-cycle duration is temperature, as it can accelerate or decelerate the rate of biochemical reactions. However, controlled experiments at the cellular scale are challenging, due to the limited availability of biocompatible temperature sensors, as well as the lack of practical methods to systematically control local temperatures and cellular dynamics. Here, we demonstrate a method to probe and control the cell-division timing in; Caenorhabditis elegans; embryos using a combination of local laser heating and nanoscale thermometry. Local infrared laser illumination produces a temperature gradient across the embryo, which is precisely measured by in vivo nanoscale thermometry using quantum defects in nanodiamonds. These techniques enable selective, controlled acceleration of the cell divisions, even enabling an inversion of division order at the two-cell stage. Our data suggest that the cell-cycle timing asynchrony of the early embryonic development in; C. elegans; is determined independently by individual cells rather than via cell-to-cell communication. Our method can be used to control the development of multicellular organisms and to provide insights into the regulation of cell-division timings as a consequence of local perturbations.
Publisher National Academy of Sciences
ISSN/ISBN 0027-8424 ; 1091-6490
URL https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/32541064/
edoc-URL https://edoc.unibas.ch/84360/
Full Text on edoc Restricted
Digital Object Identifier DOI 10.1073/pnas.1922730117
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/32541064
ISI-Number WOS:000548159300008
Document type (ISI) Journal Article
 
   

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03/05/2024