1997
DOI: 10.1897/1551-5028(1997)016<0543:aivrtc>2.3.co;2
|View full text |Cite
|
Sign up to set email alerts
|

An in Vitro Rainbow Trout Cell Bioassay for Aryl Hydrocarbon Receptor-Mediated Toxins

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

2
29
0

Year Published

1997
1997
2014
2014

Publication Types

Select...
8

Relationship

4
4

Authors

Journals

citations
Cited by 13 publications
(31 citation statements)
references
References 0 publications
2
29
0
Order By: Relevance
“…Example data set III (Fig. 3c) was generated using the RLT 2.0 bioassay, which utilizes rainbow trout hepatoma cells trans‐fected with a luciferase reporter gene under control of dioxin responsive elements to screen for Ah receptor‐active compounds [30,31]. Extracts from sediments collected from a su‐perfund site contaminated with Aroclor® 1268 (Monsanto, St. Louis, MO, USA) were analyzed.…”
Section: Methodsmentioning
confidence: 99%
“…Example data set III (Fig. 3c) was generated using the RLT 2.0 bioassay, which utilizes rainbow trout hepatoma cells trans‐fected with a luciferase reporter gene under control of dioxin responsive elements to screen for Ah receptor‐active compounds [30,31]. Extracts from sediments collected from a su‐perfund site contaminated with Aroclor® 1268 (Monsanto, St. Louis, MO, USA) were analyzed.…”
Section: Methodsmentioning
confidence: 99%
“…MVLN cells are MCF‐7 human breast carcinoma cells stably transfected with a luciferase reporter gene under control of estrogen response elements of the Xenopus vitellogenin A2 gene [23]. H4IIE‐luc cells and RLT 2.0 cells are rat and rainbow trout hepatoma cells, respectively, which were stably transfected with a luciferase reporter gene under control of dioxin‐responsive enhancers (DREs) [20,24]. All cells were cultured in 100‐mm disposable petri plates (Corning, Corning, NY, USA) and were incubated in a humidified 95:5 air:CO 2 atmosphere.…”
Section: Methodsmentioning
confidence: 99%
“…A similar system was generated previously in carp cells (Muñoz et al, 2005;Rocha et al, 2004). Single recombinant cell lines producing luciferase had been established in the past as a tool to study specific sequences, to monitor toxicity of samples to fish cells (Richter et al, 1997) or to study signalling mechanisms but the transgene was always a reporter gene luciferase linked to a regulatory sequence or encoding an endogenous gene (Collet et al, 2004;Collet and Secombes, 2005;Martin et al, 2008). Previous attempts to force fish cell to produce ISAV proteins using plasmids with strong promoters such as CMV failed to produce any recombinant cells probably because of the toxicity of the viral proteins.…”
mentioning
confidence: 99%