Literature DB >> 33828140

Fluorescence based rapid optical volume screening system (OVSS) for interrogating multicellular organisms.

Jigmi Basumatary1, Tarannum Ara1, Amartya Mukherjee2, Debanjan Dutta2, Upendra Nongthomba2, Partha Pratim Mondal3.   

Abstract

Continuous monitoring of large specimens for long durations requires fast volume imaging. This is essential for understanding the processes occurring during the developmental stages of multicellular organisms. One of the key obstacles of fluorescence based prolonged monitoring and data collection is photobleaching. To capture the biological processes and simultaneously overcome the effect of bleaching, we developed single- and multi-color lightsheet based OVSS imaging technique that enables rapid screening of multiple tissues in an organism. Our approach based on OVSS imaging employs quantized step rotation of the specimen to record 2D angular data that reduces data acquisition time when compared to the existing light sheet imaging system (SPIM). A co-planar multicolor light sheet PSF is introduced to illuminate the tissues labelled with spectrally-separated fluorescent probes. The detection is carried out using a dual-channel sub-system that can simultaneously record spectrally separate volume stacks of the target organ. Arduino-based control systems were employed to automatize and control the volume data acquisition process. To illustrate the advantages of our approach, we have noninvasively imaged the Drosophila larvae and Zebrafish embryo. Dynamic studies of multiple organs (muscle and yolk-sac) in Zebrafish for a prolonged duration (5 days) were carried out to understand muscle structuring (Dystrophin, microfibers), primitive Macrophages (in yolk-sac) and inter-dependent lipid and protein-based metabolism. The volume-based study, intensity line-plots and inter-dependence ratio analysis allowed us to understand the transition from lipid-based metabolism to protein-based metabolism during early development (Pharyngula period with a critical transition time, [Formula: see text] h post-fertilization) in Zebrafish. The advantage of multicolor lightsheet illumination, fast volume scanning, simultaneous visualization of multiple organs and an order-less photobleaching makes OVSS imaging the system of choice for rapid monitoring and real-time assessment of macroscopic biological organisms with microscopic resolution.

Entities:  

Year:  2021        PMID: 33828140     DOI: 10.1038/s41598-021-86951-3

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  33 in total

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Authors:  Valentin Magidson; Alexey Khodjakov
Journal:  Methods Cell Biol       Date:  2013       Impact factor: 1.441

8.  LITE microscopy: Tilted light-sheet excitation of model organisms offers high resolution and low photobleaching.

Authors:  Tanner C Fadero; Therese M Gerbich; Kishan Rana; Aussie Suzuki; Matthew DiSalvo; Kristina N Schaefer; Jennifer K Heppert; Thomas C Boothby; Bob Goldstein; Mark Peifer; Nancy L Allbritton; Amy S Gladfelter; Amy S Maddox; Paul S Maddox
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9.  Zebrafish: an emerging real-time model system to study Alzheimer's disease and neurospecific drug discovery.

Authors:  Suraiya Saleem; Rajaretinam Rajesh Kannan
Journal:  Cell Death Discov       Date:  2018-10-03

10.  Loss of embryonic neural crest derived cardiomyocytes causes adult onset hypertrophic cardiomyopathy in zebrafish.

Authors:  Sarah Abdul-Wajid; Bradley L Demarest; H Joseph Yost
Journal:  Nat Commun       Date:  2018-11-02       Impact factor: 14.919

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  1 in total

1.  Lightsheet optical tweezer (LOT) for optical manipulation of microscopic particles and live cells.

Authors:  Partha Pratim Mondal; Neptune Baro; Ankur Singh; Prakash Joshi; Jigmi Basumatary
Journal:  Sci Rep       Date:  2022-06-17       Impact factor: 4.996

  1 in total

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