| Literature DB >> 27235815 |
Maria Angels de Luis Balaguer1, Marina Ramos-Pezzotti1, Morjan B Rahhal2, Charles E Melvin3, Eva Johannes4, Timothy J Horn5, Rosangela Sozzani6.
Abstract
Time-course imaging experiments on live organisms are critical for understanding the dynamics of growth and development. Light-sheet microscopy has advanced the field of long-term imaging of live specimens by significantly reducing photo-toxicity and allowing fast acquisition of three-dimensional data over time. However, current light-sheet technology does not allow the imaging of multiple plant specimens in parallel. To achieve higher throughput, we have developed a Multi-sample Arabidopsis Growth and Imaging Chamber (MAGIC) that provides near-physiological imaging conditions and allows high-throughput time-course imaging experiments in the ZEISS Lightsheet Z.1. Here, we illustrate MAGIC's imaging capabilities by following cell divisions, as an indicator of plant growth and development, over prolonged time periods. To automatically quantify the number of cell divisions in long-term experiments, we present a FIJI-based image processing pipeline. We demonstrate that plants imaged with our chamber undergo cell divisions for >16 times longer than those with the glass capillary system supplied by the ZEISS Z1.Entities:
Keywords: 3D printing; Arabidopsis root; Light sheet; Time-lapse imaging
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Year: 2016 PMID: 27235815 DOI: 10.1016/j.ydbio.2016.05.029
Source DB: PubMed Journal: Dev Biol ISSN: 0012-1606 Impact factor: 3.582