Literature DB >> 30406156

6-hydroxydopamine (6-OHDA) Oxidative Stress Assay for Observing Dopaminergic Neuron Loss in Caenorhabditis elegans.

Sarah-Lena Offenburger1, Anton Gartner1.   

Abstract

The nematode Caenorhabditis elegans is a powerful genetic model that can be used to investigate neuronal death. Research using C. elegans has been crucial to characterize cell death programmes that are conserved in mammals. Many neuronal signaling components, such as those mediating dopaminergic neurotransmission, are preserved as well. Dopaminergic neurons are progressively lost in Parkinson's disease and an important risk factor to develop this disease appears to be oxidative stress, the increased occurrence of highly reactive oxygen species. Oxidative stress-induced dopaminergic neurodegeneration is mimicked in animal models by treatment with 6-hydroxydopamine (6-OHDA), a dopamine analog, which is specifically taken up into dopaminergic neurons. After exposing C. elegans to 6-OHDA, the loss of fluorescently labeled dopaminergic neurons can be easily monitored. An organisms' sensitivity to oxidative stress is thought to be influenced by basal levels of intrinsic oxidative stress and the ability to counteract oxidative stress and oxidative stress-induced damage. The C. elegans '6-OHDA model' led to the discovery of novel genes that are required to protect dopaminergic neurons and it has helped to determine the effects of conserved cell death and cell engulfment pathways in dopaminergic neurodegeneration. Here, we describe a simple protocol that allows for the easy detection of dopaminergic neuron loss after 6-OHDA treatment in C. elegans.

Entities:  

Keywords:  6-OHDA; 6-hydroxydopamine; C. elegans; Caenorhabditis elegans; Dopaminergic neurodegeneration; Intoxication; Oxidative stress assay

Year:  2018        PMID: 30406156      PMCID: PMC6218003          DOI: 10.21769/BioProtoc.3025

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  11 in total

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Journal:  J Comp Neurol       Date:  1975-09-15       Impact factor: 3.215

2.  Modeling dopamine neuron degeneration in Caenorhabditis elegans.

Authors:  Michelle L Tucci; Adam J Harrington; Guy A Caldwell; Kim A Caldwell
Journal:  Methods Mol Biol       Date:  2011

Review 3.  Classic toxin-induced animal models of Parkinson's disease: 6-OHDA and MPTP.

Authors:  Andreas Schober
Journal:  Cell Tissue Res       Date:  2004-07-28       Impact factor: 5.249

4.  Influence of autophagy genes on ion-channel-dependent neuronal degeneration in Caenorhabditis elegans.

Authors:  Márton L Tóth; Péter Simon; Attila L Kovács; Tibor Vellai
Journal:  J Cell Sci       Date:  2007-02-27       Impact factor: 5.285

5.  C. elegans: a novel pharmacogenetic model to study Parkinson's disease.

Authors:  R Nass; D M. Miller; R D. Blakely
Journal:  Parkinsonism Relat Disord       Date:  2001-07       Impact factor: 4.891

6.  The genetics of Caenorhabditis elegans.

Authors:  S Brenner
Journal:  Genetics       Date:  1974-05       Impact factor: 4.562

7.  Tetraspanin (TSP-17) protects dopaminergic neurons against 6-OHDA-induced neurodegeneration in C. elegans.

Authors:  Neda Masoudi; Pablo Ibanez-Cruceyra; Sarah-Lena Offenburger; Alexander Holmes; Anton Gartner
Journal:  PLoS Genet       Date:  2014-12-04       Impact factor: 5.917

8.  Exposure to mitochondrial genotoxins and dopaminergic neurodegeneration in Caenorhabditis elegans.

Authors:  Claudia P González-Hunt; Maxwell C K Leung; Rakesh K Bodhicharla; Madeline G McKeever; Andrew E Arrant; Kathleen M Margillo; Ian T Ryde; Derek D Cyr; Sara G Kosmaczewski; Marc Hammarlund; Joel N Meyer
Journal:  PLoS One       Date:  2014-12-08       Impact factor: 3.240

9.  Mutations in Caenorhabditis elegans neuroligin-like glit-1, the apoptosis pathway and the calcium chaperone crt-1 increase dopaminergic neurodegeneration after 6-OHDA treatment.

Authors:  Sarah-Lena Offenburger; Elisabeth Jongsma; Anton Gartner
Journal:  PLoS Genet       Date:  2018-01-18       Impact factor: 5.917

10.  6-OHDA-induced dopaminergic neurodegeneration in Caenorhabditis elegans is promoted by the engulfment pathway and inhibited by the transthyretin-related protein TTR-33.

Authors:  Sarah-Lena Offenburger; Xue Yan Ho; Theresa Tachie-Menson; Sean Coakley; Massimo A Hilliard; Anton Gartner
Journal:  PLoS Genet       Date:  2018-01-18       Impact factor: 5.917

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