Literature DB >> 15004740

Imaging plant cells by two-photon excitation.

José A Feijó1, Nuno Moreno.   

Abstract

Along the past recent years, two-photon excitation (TPE) microscopy has moved from the realms of technical curiosity to be a standard application in many advanced cell biology laboratories. The growing body of literature covered in this review points out the obvious advantages of TPE over any other imaging method based on fluorescence, clearly improving signal-to-noise ratio and thick-tissue penetration and showing added potential for vital imaging. Like any new technology that has to gain its own space, TPE microscopy is still going through the growing pains in which reproducible protocols, probes, and applications are scarce. Yet, the published reports and unpublished results covered in this review point out that TPE can eventually accommodate most available protocols and probes, most of the times with evident advantages. Further, the potential for plant sciences is obvious, as plant cells possess many absorbing molecules and structures and are routinely more opaque than tissues of other organisms. Since prices make it one of the most expensive microscopies, TPE is coming slow to be a generalised technology, but enough data are emerging to establish it as a method with no alternative for some objectives.

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Year:  2004        PMID: 15004740     DOI: 10.1007/s00709-003-0026-2

Source DB:  PubMed          Journal:  Protoplasma        ISSN: 0033-183X            Impact factor:   3.356


  28 in total

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2.  Emergence and patterning of the five cell types of the Zea mays anther locule.

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Journal:  Dev Biol       Date:  2010-11-09       Impact factor: 3.582

3.  Enlightenment by the invisible.

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Journal:  Protoplasma       Date:  2015-09-05       Impact factor: 3.356

4.  Exclusion of a proton ATPase from the apical membrane is associated with cell polarity and tip growth in Nicotiana tabacum pollen tubes.

Authors:  Ana C Certal; Ricardo B Almeida; Lara M Carvalho; Eric Wong; Nuno Moreno; Erwan Michard; Jorge Carneiro; Joaquín Rodriguéz-Léon; Hen-Ming Wu; Alice Y Cheung; José A Feijó
Journal:  Plant Cell       Date:  2008-03-25       Impact factor: 11.277

5.  Imaging of multi-color fluorescence emission from leaf tissues.

Authors:  Zuzana Benediktyová; Ladislav Nedbal
Journal:  Photosynth Res       Date:  2009-09-26       Impact factor: 3.573

Review 6.  Optical microscopy in photosynthesis.

Authors:  Richard Cisek; Leigh Spencer; Nicole Prent; Donatas Zigmantas; George S Espie; Virginijus Barzda
Journal:  Photosynth Res       Date:  2009-10-23       Impact factor: 3.573

7.  An optical clearing technique for plant tissues allowing deep imaging and compatible with fluorescence microscopy.

Authors:  Cherish A Warner; Meredith L Biedrzycki; Samuel S Jacobs; Randall J Wisser; Jeffrey L Caplan; D Janine Sherrier
Journal:  Plant Physiol       Date:  2014-10-24       Impact factor: 8.340

8.  Fluorescent Labeling and Confocal Microcopy of Plastids and Stromules.

Authors:  Maureen R Hanson; Patricia L Conklin; Amirali Sattarzadeh
Journal:  Methods Mol Biol       Date:  2021

9.  Influence of Vacuum Cooling on Escherichia coli O157:H7 Infiltration in Fresh Leafy Greens via a Multiphoton-Imaging Approach.

Authors:  Erica Vonasek; Nitin Nitin
Journal:  Appl Environ Microbiol       Date:  2015-10-16       Impact factor: 4.792

10.  High-contrast three-dimensional imaging of the Arabidopsis leaf enables the analysis of cell dimensions in the epidermis and mesophyll.

Authors:  Nathalie Wuyts; Jean-Christophe Palauqui; Geneviève Conejero; Jean-Luc Verdeil; Christine Granier; Catherine Massonnet
Journal:  Plant Methods       Date:  2010-07-02       Impact factor: 4.993

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