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A promising new wavelength region for three-photon fluorescence microscopy of live cells

We report three-photon laser scanning microscopy (3PLSM) using a bi-directional pumped optical parametric oscillator (OPO) with signal wavelength output at λ= 1500 nm. This novel laser was used to overcome the high optical loss in the infrared spectral region observed in laser scanning microscopes a...

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Detalles Bibliográficos
Autores principales: Norris, Greg, Amor, Rumelo, Dempster, John, Amos, William B, McConnell, Gail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664407/
https://www.ncbi.nlm.nih.gov/pubmed/22458977
http://dx.doi.org/10.1111/j.1365-2818.2012.03610.x
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author Norris, Greg
Amor, Rumelo
Dempster, John
Amos, William B
McConnell, Gail
author_facet Norris, Greg
Amor, Rumelo
Dempster, John
Amos, William B
McConnell, Gail
author_sort Norris, Greg
collection PubMed
description We report three-photon laser scanning microscopy (3PLSM) using a bi-directional pumped optical parametric oscillator (OPO) with signal wavelength output at λ= 1500 nm. This novel laser was used to overcome the high optical loss in the infrared spectral region observed in laser scanning microscopes and objective lenses that renders them otherwise difficult to use for imaging. To test our system, we performed 3PLSM auto-fluorescence imaging of live plant cells at λ= 1500 nm, specifically Spirogyra, and compared performance with two-photon excitation (2PLSM) imaging using a femtosecond pulsed Ti:Sapphire laser at λ= 780 nm. Analysis of cell viability based on cytoplasmic organelle streaming and structural changes of cells revealed that at similar peak powers, 2PLSM caused gross cell damage after 5 min but 3PLSM showed little or no interference with cell function after 15 min. The λ= 1500 nm OPO is thus shown to be a practical laser source for live cell imaging.
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spelling pubmed-36644072013-06-03 A promising new wavelength region for three-photon fluorescence microscopy of live cells Norris, Greg Amor, Rumelo Dempster, John Amos, William B McConnell, Gail J Microsc Original Articles We report three-photon laser scanning microscopy (3PLSM) using a bi-directional pumped optical parametric oscillator (OPO) with signal wavelength output at λ= 1500 nm. This novel laser was used to overcome the high optical loss in the infrared spectral region observed in laser scanning microscopes and objective lenses that renders them otherwise difficult to use for imaging. To test our system, we performed 3PLSM auto-fluorescence imaging of live plant cells at λ= 1500 nm, specifically Spirogyra, and compared performance with two-photon excitation (2PLSM) imaging using a femtosecond pulsed Ti:Sapphire laser at λ= 780 nm. Analysis of cell viability based on cytoplasmic organelle streaming and structural changes of cells revealed that at similar peak powers, 2PLSM caused gross cell damage after 5 min but 3PLSM showed little or no interference with cell function after 15 min. The λ= 1500 nm OPO is thus shown to be a practical laser source for live cell imaging. Blackwell Publishing Ltd 2012-06 /pmc/articles/PMC3664407/ /pubmed/22458977 http://dx.doi.org/10.1111/j.1365-2818.2012.03610.x Text en © 2012 The Authors Journal of Microscopy © 2012 Wadsworth Center, New York State Department of Health http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Norris, Greg
Amor, Rumelo
Dempster, John
Amos, William B
McConnell, Gail
A promising new wavelength region for three-photon fluorescence microscopy of live cells
title A promising new wavelength region for three-photon fluorescence microscopy of live cells
title_full A promising new wavelength region for three-photon fluorescence microscopy of live cells
title_fullStr A promising new wavelength region for three-photon fluorescence microscopy of live cells
title_full_unstemmed A promising new wavelength region for three-photon fluorescence microscopy of live cells
title_short A promising new wavelength region for three-photon fluorescence microscopy of live cells
title_sort promising new wavelength region for three-photon fluorescence microscopy of live cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664407/
https://www.ncbi.nlm.nih.gov/pubmed/22458977
http://dx.doi.org/10.1111/j.1365-2818.2012.03610.x
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