Literature DB >> 23517500

Deep UV autofluorescence microscopy for cell biology and tissue histology.

Frédéric Jamme1, Slavka Kascakova, Sandrine Villette, Fatma Allouche, Stéphane Pallu, Valérie Rouam, Matthieu Réfrégiers.   

Abstract

BACKGROUND INFORMATION: Autofluorescence spectroscopy is a powerful tool for molecular histology and for following metabolic processes in biological samples as it does not require labelling. However, at the microscopic scale, it is mostly limited to visible and near infrared excitation of the samples. Several interesting and naturally occurring fluorophores can be excited in the UV and deep UV (DUV), but cannot be monitored in cellulo nor in vivo due to a lack of available microscopic instruments working in this wavelength range. To fulfil this need, we have developed a synchrotron-coupled DUV microspectrofluorimeter which is operational since 2010. An extended selection of endogenous autofluorescent probes that can be excited in DUV, including their spectral characteristics, is presented. The distribution of the probes in various biological samples, including cultured cells, soft tissues, bone sections and maize stems, is shown to illustrate the possibilities offered by this system. In this work we demonstrate that DUV autofluorescence is a powerful tool for tissue histology and cell biology.
RESULTS: To fulfil this need, we have developed a synchrotron-coupled DUV microspectrofluorimeter which is operational since 2010. An extended selection of endogenous autofluorescent probes that can be excited in DUV, including their spectral characteristics, is presented. The distribution of the probes in various biological samples, including cultured cells, soft tissues, bone sections and maize stems, is shown to illustrate the possibilities offered by this system. In this work we demonstrate that DUV autofluorescence is a powerful tool for tissue histology and cell biology.
CONCLUSIONS: In this work we demonstrate that DUV autofluorescence is a powerful tool for tissue histology and cell biology.
© 2013 Société Française des Microscopies and Société de Biologie Cellulaire de France. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Autofluorescence; DUV; Microspectroscopy; Synchrotron; UV

Mesh:

Year:  2013        PMID: 23517500     DOI: 10.1111/boc.201200075

Source DB:  PubMed          Journal:  Biol Cell        ISSN: 0248-4900            Impact factor:   4.458


  17 in total

1.  Spectrofluorimetric quantification of antibiotic drug concentration in bacterial cells for the characterization of translocation across bacterial membranes.

Authors:  Julia Vergalli; Estelle Dumont; Jelena Pajović; Bertrand Cinquin; Laure Maigre; Muriel Masi; Matthieu Réfrégiers; Jean-Marie Pagés
Journal:  Nat Protoc       Date:  2018-05-17       Impact factor: 13.491

2.  Synchrotron Infrared and Deep UV Fluorescent Microspectroscopy Study of PB1-F2 β-Aggregated Structures in Influenza A Virus-infected Cells.

Authors:  Christophe Chevalier; Ronan Le Goffic; Frédéric Jamme; Olivier Leymarie; Matthieu Réfrégiers; Bernard Delmas
Journal:  J Biol Chem       Date:  2016-02-19       Impact factor: 5.157

3.  Deep-UV biological imaging by lanthanide ion molecular protection.

Authors:  Yasuaki Kumamoto; Katsumasa Fujita; Nicholas Isaac Smith; Satoshi Kawata
Journal:  Biomed Opt Express       Date:  2015-12-18       Impact factor: 3.732

4.  Aluminum plasmonic nanoshielding in ultraviolet inactivation of bacteria.

Authors:  Jeremy N Kunz; Dmitri V Voronine; Weigang Lu; Zachary Liege; Ho Wai Howard Lee; Zhenrong Zhang; Marlan O Scully
Journal:  Sci Rep       Date:  2017-08-22       Impact factor: 4.379

5.  Characterization of Pustular Mats and Related Rivularia-Rich Laminations in Oncoids From the Laguna Negra Lake (Argentina).

Authors:  Estela C Mlewski; Céline Pisapia; Fernando Gomez; Lena Lecourt; Eliana Soto Rueda; Karim Benzerara; Bénédicte Ménez; Stephan Borensztajn; Frédéric Jamme; Matthieu Réfrégiers; Emmanuelle Gérard
Journal:  Front Microbiol       Date:  2018-05-22       Impact factor: 5.640

6.  Synchrotron Time-Lapse Imaging of Lignocellulosic Biomass Hydrolysis: Tracking Enzyme Localization by Protein Autofluorescence and Biochemical Modification of Cell Walls by Microfluidic Infrared Microspectroscopy.

Authors:  Marie-Françoise Devaux; Frédéric Jamme; William André; Brigitte Bouchet; Camille Alvarado; Sylvie Durand; Paul Robert; Luc Saulnier; Estelle Bonnin; Fabienne Guillon
Journal:  Front Plant Sci       Date:  2018-02-20       Impact factor: 5.753

7.  Synchrotron multimodal imaging in a whole cell reveals lipid droplet core organization.

Authors:  Frédéric Jamme; Bertrand Cinquin; Yann Gohon; Eva Pereiro; Matthieu Réfrégiers; Marine Froissard
Journal:  J Synchrotron Radiat       Date:  2020-04-23       Impact factor: 2.616

8.  Microspectrometric insights on the uptake of antibiotics at the single bacterial cell level.

Authors:  Bertrand Cinquin; Laure Maigre; Elizabeth Pinet; Jacqueline Chevalier; Robert A Stavenger; Scott Mills; Matthieu Réfrégiers; Jean-Marie Pagès
Journal:  Sci Rep       Date:  2015-12-11       Impact factor: 4.379

9.  Histological quantification of maize stem sections from FASGA-stained images.

Authors:  David Legland; Fadi El-Hage; Valérie Méchin; Matthieu Reymond
Journal:  Plant Methods       Date:  2017-11-01       Impact factor: 4.993

10.  Imaging and Spectroscopy of Natural Fluorophores in Pine Needles.

Authors:  Lloyd Donaldson; Nari Williams
Journal:  Plants (Basel)       Date:  2018-02-02
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