Literature DB >> 16458361

Ultrafast random-access scanning in two-photon microscopy using acousto-optic deflectors.

R Salomé1, Y Kremer, S Dieudonné, J-F Léger, O Krichevsky, C Wyart, D Chatenay, L Bourdieu.   

Abstract

Two-photon scanning microscopy (TPSM) is a powerful tool for imaging deep inside living tissues with sub-cellular resolution. The temporal resolution of TPSM is however strongly limited by the galvanometric mirrors used to steer the laser beam. Fast physiological events can therefore only be followed by scanning repeatedly a single line within the field of view. Because acousto-optic deflectors (AODs) are non-mechanical devices, they allow access at any point within the field of view on a microsecond time scale and are therefore excellent candidates to improve the temporal resolution of TPSM. However, the use of AOD-based scanners with femtosecond pulses raises several technical difficulties. In this paper, we describe an all-digital TPSM setup based on two crossed AODs. It includes in particular an acousto-optic modulator (AOM) placed at 45 degrees with respect to the AODs to pre-compensate for the large spatial distortions of femtosecond pulses occurring in the AODs, in order to optimize the spatial resolution and the fluorescence excitation. Our setup allows recording from freely selectable point-of-interest at high speed (1kHz). By maximizing the time spent on points of interest, random-access TPSM (RA-TPSM) constitutes a promising method for multiunit recordings with millisecond resolution in biological tissues.

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Mesh:

Year:  2006        PMID: 16458361     DOI: 10.1016/j.jneumeth.2005.12.010

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  49 in total

1.  Fast two-photon in vivo imaging with three-dimensional random-access scanning in large tissue volumes.

Authors:  Gergely Katona; Gergely Szalay; Pál Maák; Attila Kaszás; Máté Veress; Dániel Hillier; Balázs Chiovini; E Sylvester Vizi; Botond Roska; Balázs Rózsa
Journal:  Nat Methods       Date:  2012-01-08       Impact factor: 28.547

Review 2.  Two-photon microscopy as a tool to study blood flow and neurovascular coupling in the rodent brain.

Authors:  Andy Y Shih; Jonathan D Driscoll; Patrick J Drew; Nozomi Nishimura; Chris B Schaffer; David Kleinfeld
Journal:  J Cereb Blood Flow Metab       Date:  2012-02-01       Impact factor: 6.200

Review 3.  Imaging calcium signals in vivo: a powerful tool in physiology and pharmacology.

Authors:  James T Russell
Journal:  Br J Pharmacol       Date:  2011-08       Impact factor: 8.739

4.  Method to reconstruct neuronal action potential train from two-photon calcium imaging.

Authors:  Tingwei Quan; Xiuli Liu; Xiaohua Lv; Wei R Chen; Shaoqun Zeng
Journal:  J Biomed Opt       Date:  2010 Nov-Dec       Impact factor: 3.170

5.  Ultrafast, temporally stochastic STED nanoscopy of millisecond dynamics.

Authors:  Jale Schneider; Jasmin Zahn; Marta Maglione; Stephan J Sigrist; Jonas Marquard; Jakub Chojnacki; Hans-Georg Kräusslich; Steffen J Sahl; Johann Engelhardt; Stefan W Hell
Journal:  Nat Methods       Date:  2015-07-27       Impact factor: 28.547

6.  High-throughput spatial light modulation two-photon microscopy for fast functional imaging.

Authors:  Paolo Pozzi; Daniela Gandolfi; Marialuisa Tognolina; Giuseppe Chirico; Jonathan Mapelli; Egidio D'Angelo
Journal:  Neurophotonics       Date:  2015-02-09       Impact factor: 3.593

7.  Two-photon imaging of spatially extended neuronal network dynamics with high temporal resolution.

Authors:  Kyle P Lillis; Alfred Eng; John A White; Jerome Mertz
Journal:  J Neurosci Methods       Date:  2008-05-03       Impact factor: 2.390

8.  Second-harmonic generation imaging of membrane potential with photon counting.

Authors:  Jiang Jiang; Rafael Yuste
Journal:  Microsc Microanal       Date:  2008-12       Impact factor: 4.127

9.  Two-photon microscope for multisite microphotolysis of caged neurotransmitters in acute brain slices.

Authors:  Bradley E Losavio; Vijay Iyer; Peter Saggau
Journal:  J Biomed Opt       Date:  2009 Nov-Dec       Impact factor: 3.170

10.  Longitudinal in vivo two-photon fluorescence imaging.

Authors:  Sarah E Crowe; Graham C R Ellis-Davies
Journal:  J Comp Neurol       Date:  2014-06-01       Impact factor: 3.215

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