Literature DB >> 24915644

Analyzing cell physiology in C. elegans with fluorescent ratiometric reporters.

Hongning Wang1, Uma Karadge2, William H Humphries3, Alfred L Fisher4.   

Abstract

Ratiometric fluorescent reporters have recently emerged a new technique to non-invasively measure aspects of cell physiology such as redox status, calcium levels, energy production, and NADH levels. These reporters consist of either a single or pair of fluorophores along with specific modifications, such as the addition of a protein domain which binds to a metabolite of interest, thereby producing gradual alterations in fluorescence in response to changes in the measured parameter. Measurement of the changes in fluorescence produces a quantitative read-out of the cellular environment. While these reporters were initially developed to easily visualize and track changes in cultured cells, several groups have adapted these reporters to use in Caenorhabditis elegans which opens a new avenue through which to explore cell physiology during development or aging, in response to changes in external environment, or in response to genetic manipulation. These reporters have the advantage of being easily targeted to any part of the worm, and because C. elegans is transparent both the reporters and changes in their fluorescence can be clearly observed in vivo. Here we discuss the application of ratiometric reporters to C. elegans, and outline a method to quantitatively measure changes in intracellular peroxide levels using the HyPer ratiometric reporter. However, these principles can be applied to alternate ratiometric reporters which are designed to measure either other chemical species or other cellular parameters. Published by Elsevier Inc.

Entities:  

Keywords:  Caenorhabditis elegans; Digital imaging; Fluorescent proteins; Metabolism; Ratiometric reporters; Transgene

Mesh:

Substances:

Year:  2014        PMID: 24915644      PMCID: PMC4118691          DOI: 10.1016/j.ymeth.2014.05.012

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  59 in total

1.  Monitoring protein conformations and interactions by fluorescence resonance energy transfer between mutants of green fluorescent protein.

Authors:  A Miyawaki; R Y Tsien
Journal:  Methods Enzymol       Date:  2000       Impact factor: 1.600

2.  Genetically encoded fluorescent reporters of protein tyrosine kinase activities in living cells.

Authors:  A Y Ting; K H Kain; R L Klemke; R Y Tsien
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-18       Impact factor: 11.205

3.  Imaging dynamic redox changes in mammalian cells with green fluorescent protein indicators.

Authors:  Colette T Dooley; Timothy M Dore; George T Hanson; W Coyt Jackson; S James Remington; Roger Y Tsien
Journal:  J Biol Chem       Date:  2004-02-25       Impact factor: 5.157

4.  A calcineurin homologous protein is required for sodium-proton exchange events in the C. elegans intestine.

Authors:  Jamie Wagner; Erik Allman; Ashley Taylor; Kiri Ulmschneider; Timothy Kovanda; Bryne Ulmschneider; Keith Nehrke; Maureen A Peters
Journal:  Am J Physiol Cell Physiol       Date:  2011-08-24       Impact factor: 4.249

5.  The OhrR repressor senses organic hydroperoxides by reversible formation of a cysteine-sulfenic acid derivative.

Authors:  Mayuree Fuangthong; John D Helmann
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-30       Impact factor: 11.205

6.  Basic Caenorhabditis elegans methods: synchronization and observation.

Authors:  Montserrat Porta-de-la-Riva; Laura Fontrodona; Alberto Villanueva; Julián Cerón
Journal:  J Vis Exp       Date:  2012-06-10       Impact factor: 1.355

7.  Fluorescent biosensor for quantitative real-time measurements of inositol 1,4,5-trisphosphate in single living cells.

Authors:  Akihiko Tanimura; Akihiro Nezu; Takao Morita; R James Turner; Yosuke Tojyo
Journal:  J Biol Chem       Date:  2004-07-22       Impact factor: 5.157

8.  A reduction in intestinal cell pHi due to loss of the Caenorhabditis elegans Na+/H+ exchanger NHX-2 increases life span.

Authors:  Keith Nehrke
Journal:  J Biol Chem       Date:  2003-08-25       Impact factor: 5.157

9.  Visualization of ATP levels inside single living cells with fluorescence resonance energy transfer-based genetically encoded indicators.

Authors:  Hiromi Imamura; Kim P Huynh Nhat; Hiroko Togawa; Kenta Saito; Ryota Iino; Yasuyuki Kato-Yamada; Takeharu Nagai; Hiroyuki Noji
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-31       Impact factor: 11.205

Review 10.  Use of chimeric fluorescent proteins and fluorescence resonance energy transfer to monitor cellular responses.

Authors:  Manuela Zaccolo
Journal:  Circ Res       Date:  2004-04-16       Impact factor: 17.367

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  4 in total

1.  Expanding the C. elegans toolbox into a toolshed.

Authors:  Arjumand Ghazi; Judith Yanowitz; Gary A Silverman
Journal:  Methods       Date:  2014-08-01       Impact factor: 3.608

2.  In Vivo Detection of Reactive Oxygen Species and Redox Status in Caenorhabditis elegans.

Authors:  Bart P Braeckman; Arne Smolders; Patricia Back; Sasha De Henau
Journal:  Antioxid Redox Signal       Date:  2016-09-12       Impact factor: 8.401

3.  Evaluation of the antioxidant property and effects in Caenorhabditis elegans of Xiangxi flavor vinegar, a Hunan local traditional vinegar.

Authors:  Run-Ting Huang; Qing Huang; Gen-Liang Wu; Chun-Guang Chen; Zong-Jun Li
Journal:  J Zhejiang Univ Sci B       Date:  2017 Apr.       Impact factor: 3.066

4.  Cell-autonomous and non-autonomous roles of daf-16 in muscle function and mitochondrial capacity in aging C. elegans.

Authors:  Hongning Wang; Phillip Webster; Lizhen Chen; Alfred L Fisher
Journal:  Aging (Albany NY)       Date:  2019-04-24       Impact factor: 5.682

  4 in total

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