Literature DB >> 16543762

Principles of multiphoton microscopy.

Kenneth W Dunn1, Pamela A Young.   

Abstract

Multiphoton fluorescence microscopy is a powerful, important tool in biomedical research that offers low photon toxicity and higher spatial and temporal resolution than other in vivo imaging modalities. The capability to collect images hundreds of micrometers into biological tissues provides an invaluable tool for studying cellular and subcellular processes in the context of tissues and organs in living animals. Multiphoton microscopy is based upon two-photon excitation of fluorescence that occurs only in a sub-femtoliter volume at the focus; by scanning the focus through a sample, 2- and 3-dimensional images can be collected. The complex 3-dimensional organization of the kidney makes it especially appropriate for multiphoton microscopic analysis, which has been used to characterize numerous aspects of renal physiology and pathophysiology in living rats and mice. However, the ability to collect fluorescence images deep into biological tissues raises unique problems not encountered in other forms of optical microscopy, including issues of probe access, and tissue optics. Future improvements in multiphoton fluorescence microscopy will involve optimizing objectives for the unique characteristics of multiphoton fluorescence imaging, improving the speed at which images may be collected and extending the depth to which imaging may be conducted. Copyright 2006 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2006        PMID: 16543762     DOI: 10.1159/000090614

Source DB:  PubMed          Journal:  Nephron Exp Nephrol        ISSN: 1660-2129


  26 in total

1.  The role of backscattering in SHG tissue imaging.

Authors:  François Légaré; Christian Pfeffer; Bjorn R Olsen
Journal:  Biophys J       Date:  2007-04-20       Impact factor: 4.033

2.  Improving Signal Levels in Intravital Multiphoton Microscopy using an Objective Correction Collar.

Authors:  Pamela A Muriello; Kenneth W Dunn
Journal:  Opt Commun       Date:  2008-04-01       Impact factor: 2.310

3.  Techniques to study nephron function: microscopy and imaging.

Authors:  Bruce A Molitoris; Ruben M Sandoval
Journal:  Pflugers Arch       Date:  2009-01-15       Impact factor: 3.657

Review 4.  Deep insights: intravital imaging with two-photon microscopy.

Authors:  Ina Maria Schießl; Hayo Castrop
Journal:  Pflugers Arch       Date:  2016-06-28       Impact factor: 3.657

5.  A pragmatic guide to multiphoton microscope design.

Authors:  Michael D Young; Jeffrey J Field; Kraig E Sheetz; Randy A Bartels; Jeff Squier
Journal:  Adv Opt Photonics       Date:  2015-06-30       Impact factor: 20.107

Review 6.  Real-time intravital imaging of cancer models.

Authors:  A Zomer; E Beerling; E J Vlug; J van Rheenen
Journal:  Clin Transl Oncol       Date:  2011-12       Impact factor: 3.405

Review 7.  Two-photon microscopy in pulmonary research.

Authors:  Ruben G Nava; Wenjun Li; Andrew E Gelman; Alexander S Krupnick; Mark J Miller; Daniel Kreisel
Journal:  Semin Immunopathol       Date:  2010-06-30       Impact factor: 9.623

Review 8.  In vivo microscopy.

Authors:  János Peti-Peterdi
Journal:  Nephrol Ther       Date:  2016-03-08       Impact factor: 0.722

9.  Multimodal nonlinear optical imaging of collagen arrays.

Authors:  Christian P Pfeffer; Bjorn R Olsen; Feruz Ganikhanov; François Légaré
Journal:  J Struct Biol       Date:  2008-07-11       Impact factor: 2.867

10.  Live-animal imaging of renal function by multiphoton microscopy.

Authors:  Kenneth W Dunn; Timothy A Sutton; Ruben M Sandoval
Journal:  Curr Protoc Cytom       Date:  2012-10
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