| Literature DB >> 28041904 |
Wolfgang Keil1, Lena M Kutscher2, Shai Shaham3, Eric D Siggia4.
Abstract
Long-term studies of Caenorhabditis elegans larval development traditionally require tedious manual observations because larvae must move to develop, and existing immobilization techniques either perturb development or are unsuited for young larvae. Here, we present a simple microfluidic device to simultaneously follow development of ten C. elegans larvae at high spatiotemporal resolution from hatching to adulthood (∼3 days). Animals grown in microchambers are periodically immobilized by compression to allow high-quality imaging of even weak fluorescence signals. Using the device, we obtain cell-cycle statistics for C. elegans vulval development, a paradigm for organogenesis. We combine Nomarski and multichannel fluorescence microscopy to study processes such as cell-fate specification, cell death, and transdifferentiation throughout post-embryonic development. Finally, we generate time-lapse movies of complex neural arborization through automated image registration. Our technique opens the door to quantitative analysis of time-dependent phenomena governing cellular behavior during C. elegans larval development.Entities:
Keywords: Caenorhabditis elegans; PDA neuron; PVD neuron; dendritic arborization; larval development; linker cell death; long-term imaging; microfluidics; transdifferentiation; vulval development
Mesh:
Year: 2016 PMID: 28041904 PMCID: PMC5263027 DOI: 10.1016/j.devcel.2016.11.022
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270