Literature DB >> 26613986

Caenorhabditis elegans, a Biological Model for Research in Toxicology.

Lesly Tejeda-Benitez1, Jesus Olivero-Verbel2.   

Abstract

Caenorhabditis elegans is a nematode of microscopic size which, due to its biological characteristics, has been used since the 1970s as a model for research in molecular biology, medicine, pharmacology, and toxicology. It was the first animal whose genome was completely sequenced and has played a key role in the understanding of apoptosis and RNA interference. The transparency of its body, short lifespan, ability to self-fertilize and ease of culture are advantages that make it ideal as a model in toxicology. Due to the fact that some of its biochemical pathways are similar to those of humans, it has been employed in research in several fields. C. elegans' use as a biological model in environmental toxicological assessments allows the determination of multiple endpoints. Some of these utilize the effects on the biological functions of the nematode and others use molecular markers. Endpoints such as lethality, growth, reproduction, and locomotion are the most studied, and usually employ the wild type Bristol N2 strain. Other endpoints use reporter genes, such as green fluorescence protein, driven by regulatory sequences from other genes related to different mechanisms of toxicity, such as heat shock, oxidative stress, CYP system, and metallothioneins among others, allowing the study of gene expression in a manner both rapid and easy. These transgenic strains of C. elegans represent a powerful tool to assess toxicity pathways for mixtures and environmental samples, and their numbers are growing in diversity and selectivity. However, other molecular biology techniques, including DNA microarrays and MicroRNAs have been explored to assess the effects of different toxicants and samples. C. elegans has allowed the assessment of neurotoxic effects for heavy metals and pesticides, among those more frequently studied, as the nematode has a very well defined nervous system. More recently, nanoparticles are emergent pollutants whose toxicity can be explored using this nematode. Overall, almost every type of known toxicant has been tested with this animal model. In the near future, the available knowledge on the life cycle of C. elegans should allow more studies on reproduction and transgenerational toxicity for newly developed chemicals and materials, facilitating their introduction in the market. The great diversity of endpoints and possibilities of this animal makes it an easy first-choice for rapid toxicity screening or to detail signaling pathways involved in mechanisms of toxicity.

Entities:  

Keywords:  Biological model; Nematode; Pollutants; Reproduction; Transgenic strains

Mesh:

Year:  2016        PMID: 26613986     DOI: 10.1007/978-3-319-23573-8_1

Source DB:  PubMed          Journal:  Rev Environ Contam Toxicol        ISSN: 0179-5953            Impact factor:   7.563


  19 in total

1.  Zebrafish CYP1A expression in transgenic Caenorhabditis elegans protects from exposures to benzo[a]pyrene and a complex polycyclic aromatic hydrocarbon mixture.

Authors:  Jamie B Harris; Jessica H Hartman; Anthony L Luz; Joanna Y Wilson; Audrey Dinyari; Joel N Meyer
Journal:  Toxicology       Date:  2020-05-01       Impact factor: 4.221

Review 2.  Caenorhabditis elegans as an emerging model system in environmental epigenetics.

Authors:  Caren Weinhouse; Lisa Truong; Joel N Meyer; Patrick Allard
Journal:  Environ Mol Mutagen       Date:  2018-08-09       Impact factor: 3.216

3.  Epigenetic effects of environmental chemicals: insights from zebrafish.

Authors:  Neelakanteswar Aluru
Journal:  Curr Opin Toxicol       Date:  2017-07-14

4.  Toxicity profile of organic extracts from Magdalena River sediments.

Authors:  Lesly Tejeda-Benítez; Katia Noguera-Oviedo; Diana S Aga; Jesus Olivero-Verbel
Journal:  Environ Sci Pollut Res Int       Date:  2017-11-02       Impact factor: 4.223

Review 5.  C. elegans as a model in developmental neurotoxicology.

Authors:  Joanna A Ruszkiewicz; Adi Pinkas; Mahfuzur R Miah; Rebecca L Weitz; Michael J A Lawes; Ayodele J Akinyemi; Omamuyovwi M Ijomone; Michael Aschner
Journal:  Toxicol Appl Pharmacol       Date:  2018-03-14       Impact factor: 4.219

6.  Perfluorooctanesulfonic acid (PFOS) and perfluorobutanesulfonic acid (PFBS) impaired reproduction and altered offspring physiological functions in Caenorhabditis elegans.

Authors:  Yiren Yue; Sida Li; Zhuojia Qian; Renalison Farias Pereira; Jonghwa Lee; Jeffery J Doherty; Zhenyu Zhang; Ye Peng; John M Clark; Alicia R Timme-Laragy; Yeonhwa Park
Journal:  Food Chem Toxicol       Date:  2020-08-22       Impact factor: 6.023

7.  Comparative Analysis of Zebrafish and Planarian Model Systems for Developmental Neurotoxicity Screens Using an 87-Compound Library.

Authors:  Danielle Hagstrom; Lisa Truong; Siqi Zhang; Robert Tanguay; Eva-Maria S Collins
Journal:  Toxicol Sci       Date:  2019-01-01       Impact factor: 4.849

8.  Graphene Oxide Dysregulates Neuroligin/NLG-1-Mediated Molecular Signaling in Interneurons in Caenorhabditis elegans.

Authors:  He Chen; Huirong Li; Dayong Wang
Journal:  Sci Rep       Date:  2017-01-27       Impact factor: 4.379

Review 9.  Xenobiotic metabolism and transport in Caenorhabditis elegans.

Authors:  Jessica H Hartman; Samuel J Widmayer; Christina M Bergemann; Dillon E King; Katherine S Morton; Riccardo F Romersi; Laura E Jameson; Maxwell C K Leung; Erik C Andersen; Stefan Taubert; Joel N Meyer
Journal:  J Toxicol Environ Health B Crit Rev       Date:  2021-02-22       Impact factor: 8.071

10.  Wnt Ligands Differentially Regulate Toxicity and Translocation of Graphene Oxide through Different Mechanisms in Caenorhabditis elegans.

Authors:  Lingtong Zhi; Mingxia Ren; Man Qu; Hanyu Zhang; Dayong Wang
Journal:  Sci Rep       Date:  2016-12-13       Impact factor: 4.379

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