Literature DB >> 25360352

Wide field intravital imaging by two-photon-excitation digital-scanned light-sheet microscopy (2p-DSLM) with a high-pulse energy laser.

Atsushi Maruyama1, Yusuke Oshima2, Hiroko Kajiura-Kobayashi3, Shigenori Nonaka3, Takeshi Imamura4, Kiyoshi Naruse5.   

Abstract

Digital-scanned light-sheet microscopy (DSLM) illuminates a sample in a plane and captures single-photon-excitation fluorescence images with a camera from a direction perpendicular to the light sheet. This method is potentially useful for observing biological specimens, because image acquisition is relatively fast, resulting in reduction of phototoxicity. However, DSLM cannot be effectively applied to high-scattering materials due to the image blur resulting from thickening of the light sheet by scattered photons. However, two-photon-excitation DSLM (2p-DSLM) enables collection of high-contrast image with near infrared (NIR) excitation. In conventional 2p-DSLM, the minimal excitation volume for two-photon excitation restricts the field of view. In this study, we achieved wide-field 2p-DSLM by using a high-pulse energy fiber laser, and then used this technique to perform intravital imaging of a small model fish species, medaka (Oryzias latipes). Wide fields of view (>700 μm) were achieved by using a low-numerical aperture (NA) objective lens and high-peak energy NIR excitation at 1040 nm. We also performed high-speed imaging at near-video rate and successfully captured the heartbeat movements of a living medaka fish at 20 frames/sec.

Entities:  

Keywords:  (000.1430) Biology and medicine; (110.6880) Three-dimensional image acquisition; (180.0180) Microscopy; (180.2520) Fluorescence microscopy; (180.4315) Nonlinear microscopy

Year:  2014        PMID: 25360352      PMCID: PMC4206304          DOI: 10.1364/BOE.5.003311

Source DB:  PubMed          Journal:  Biomed Opt Express        ISSN: 2156-7085            Impact factor:   3.732


  20 in total

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4.  Controlled light-exposure microscopy reduces photobleaching and phototoxicity in fluorescence live-cell imaging.

Authors:  R A Hoebe; C H Van Oven; T W J Gadella; P B Dhonukshe; C J F Van Noorden; E M M Manders
Journal:  Nat Biotechnol       Date:  2007-01-21       Impact factor: 54.908

Review 5.  Principles of two-photon excitation fluorescence microscopy and other nonlinear imaging approaches.

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6.  Reconstruction of zebrafish early embryonic development by scanned light sheet microscopy.

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Journal:  Nat Methods       Date:  2011-07-17       Impact factor: 28.547

8.  Two-photon laser scanning fluorescence microscopy.

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9.  Light-sheet microscopy in thick media using scanned Bessel beams and two-photon fluorescence excitation.

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  8 in total

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Journal:  Rev Sci Instrum       Date:  2018-05       Impact factor: 1.523

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5.  Optimizing ultrafast illumination for multiphoton-excited fluorescence imaging.

Authors:  Caleb R Stoltzfus; Aleksander Rebane
Journal:  Biomed Opt Express       Date:  2016-04-07       Impact factor: 3.732

6.  Integrated single- and two-photon light sheet microscopy using accelerating beams.

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7.  Imaging tissue-mimic with light sheet microscopy: A comparative guideline.

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8.  Nonlinear Absorption Response Correlated to Embedded Ag Nanoparticles in BGO Single Crystal: From Two-Photon to Three-Photon Absorption.

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  8 in total

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