Supported by the EU’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 101038087. Additional funds were given by ICBAS-UPorto and by FCT (UIDB/04423/2020, UIDP/04423/2020).

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Supported by the EU’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 101038087. Additional funds were given by ICBAS-UPorto and by FCT (UIDB/04423/2020, UIDP/04423/2020).

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Publications

Testing the trout liver RTL-W1 cell line potential to study the influences of temperature on the effects of endocrine disruptors

Lopes, Celia; Teixeira, Ingrid; Raskovic, Bozidar; Rocha, Eduardo

(European Society for Comparative Endocrinology and International Society for Fish Endocrinology, 2022)

TY  - GEN
AU  - Lopes, Celia
AU  - Teixeira, Ingrid
AU  - Raskovic, Bozidar
AU  - Rocha, Eduardo
PY  - 2022
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/6939
AB  - Global warming is an undeniable reality, and one consequence is a continuous increase in the temperature of different water bodies. This phenomenon affects numerous processes in the aquatic ecosystems, including the impacts of the widely present endocrine-disrupting chemicals (EDCs). Within EDCs, ethinylestradiol (EE2) and progestins, such as levonorgestrel (LEV), are commonly detected in environmental waters. It is thus imperative to study the effects of temperature changes in the toxicology of EDCs to aquatic animals, including fish. Endocrine disruption research often relies on in vitro models, complying with the 3Rs principles. Primary hepatocytes are commonly used but also are specific and well-characterized cell lines, such as the rainbow trout liver-derived RTL-W1. This cell line presents several functional features of differentiated hepatocytes. To test the cell line potential to study the way temperature models the effects of EDCs, we exposed RTL-W1 cells (72h) to EE2, LEV or a mixture of both synthetic hormones (at 10 μM). Exposures were carried out at 18 ºC and 21 ºC, in 24-well plates, 80.000 cells per well. The cells grew at either temperature. At the end of exposures, cells were trypsinized, and the viability measured using the trypan blue exclusion assay. Cell suspensions were then centrifuged at 200 rcf, for 5 min, and pellets were frozen at -80 ºC for gene expression analysis. No differences were found in cell viability among experimental groups. The expression of two CYP P450 enzymes enrolled in xenobiotic metabolism was analyzed by qRT-PCR. The Two-way ANOVA results revealed that CYP1A was affected by temperature as its expression was lower at 18ºC than at 21ºC. As to CYP3A27 expression, it was independent of temperature but was significantly higher in the EE2 + LEV mixture compared with control and solvent control conditions. Given these results, the RTL-W1 cell line seems like a promising model to study the interactions of temperature and exposure effects of EDCs. Studies are undergoing to include genes from other relevant signalling pathways such as estrogenic, progestogenic and lipid metabolism.
PB  - European Society for Comparative Endocrinology and International Society for Fish Endocrinology
T2  - 30th CECE & 9th ISFE Joint Conference of the European Society for Comparative Endocrinology and of the International Society for Fish Endocrinology
T1  - Testing the trout liver RTL-W1 cell line potential to study the influences of temperature on the effects of endocrine disruptors
EP  - 202
SP  - 202
UR  - https://hdl.handle.net/21.15107/rcub_agrospace_6939
ER  - 
@misc{
author = "Lopes, Celia and Teixeira, Ingrid and Raskovic, Bozidar and Rocha, Eduardo",
year = "2022",
abstract = "Global warming is an undeniable reality, and one consequence is a continuous increase in the temperature of different water bodies. This phenomenon affects numerous processes in the aquatic ecosystems, including the impacts of the widely present endocrine-disrupting chemicals (EDCs). Within EDCs, ethinylestradiol (EE2) and progestins, such as levonorgestrel (LEV), are commonly detected in environmental waters. It is thus imperative to study the effects of temperature changes in the toxicology of EDCs to aquatic animals, including fish. Endocrine disruption research often relies on in vitro models, complying with the 3Rs principles. Primary hepatocytes are commonly used but also are specific and well-characterized cell lines, such as the rainbow trout liver-derived RTL-W1. This cell line presents several functional features of differentiated hepatocytes. To test the cell line potential to study the way temperature models the effects of EDCs, we exposed RTL-W1 cells (72h) to EE2, LEV or a mixture of both synthetic hormones (at 10 μM). Exposures were carried out at 18 ºC and 21 ºC, in 24-well plates, 80.000 cells per well. The cells grew at either temperature. At the end of exposures, cells were trypsinized, and the viability measured using the trypan blue exclusion assay. Cell suspensions were then centrifuged at 200 rcf, for 5 min, and pellets were frozen at -80 ºC for gene expression analysis. No differences were found in cell viability among experimental groups. The expression of two CYP P450 enzymes enrolled in xenobiotic metabolism was analyzed by qRT-PCR. The Two-way ANOVA results revealed that CYP1A was affected by temperature as its expression was lower at 18ºC than at 21ºC. As to CYP3A27 expression, it was independent of temperature but was significantly higher in the EE2 + LEV mixture compared with control and solvent control conditions. Given these results, the RTL-W1 cell line seems like a promising model to study the interactions of temperature and exposure effects of EDCs. Studies are undergoing to include genes from other relevant signalling pathways such as estrogenic, progestogenic and lipid metabolism.",
publisher = "European Society for Comparative Endocrinology and International Society for Fish Endocrinology",
journal = "30th CECE & 9th ISFE Joint Conference of the European Society for Comparative Endocrinology and of the International Society for Fish Endocrinology",
title = "Testing the trout liver RTL-W1 cell line potential to study the influences of temperature on the effects of endocrine disruptors",
pages = "202-202",
url = "https://hdl.handle.net/21.15107/rcub_agrospace_6939"
}
Lopes, C., Teixeira, I., Raskovic, B.,& Rocha, E.. (2022). Testing the trout liver RTL-W1 cell line potential to study the influences of temperature on the effects of endocrine disruptors. in 30th CECE & 9th ISFE Joint Conference of the European Society for Comparative Endocrinology and of the International Society for Fish Endocrinology
European Society for Comparative Endocrinology and International Society for Fish Endocrinology., 202-202.
https://hdl.handle.net/21.15107/rcub_agrospace_6939
Lopes C, Teixeira I, Raskovic B, Rocha E. Testing the trout liver RTL-W1 cell line potential to study the influences of temperature on the effects of endocrine disruptors. in 30th CECE & 9th ISFE Joint Conference of the European Society for Comparative Endocrinology and of the International Society for Fish Endocrinology. 2022;:202-202.
https://hdl.handle.net/21.15107/rcub_agrospace_6939 .
Lopes, Celia, Teixeira, Ingrid, Raskovic, Bozidar, Rocha, Eduardo, "Testing the trout liver RTL-W1 cell line potential to study the influences of temperature on the effects of endocrine disruptors" in 30th CECE & 9th ISFE Joint Conference of the European Society for Comparative Endocrinology and of the International Society for Fish Endocrinology (2022):202-202,
https://hdl.handle.net/21.15107/rcub_agrospace_6939 .