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Effects of 4-nitrophenol on testicular somatic cells [TM3]

ABSTRACT: These data suggested that TM3 and TM4 cells showed different responses to PNP, which might mediate different toxic mechanisms.

ORGANISM(S): Mus musculus

PROVIDER: GSE150447 | GEO | 2023/05/06

REPOSITORIES: GEO

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Effects of 4-nitrophenol on testicular somatic cells [TM4]

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Effects of 4-nitrophenol on testicular somatic cells

Project description:This SuperSeries is composed of the SubSeries listed below.

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Effects of 4-nitrophenol on testicular somatic cells

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Nitrophenol (o-nitrophenol) treatment with 3 mM for 2 h

Project description:The number and type of synthetic chemicals that are being produced worldwide continues to increase significantly. While these industrial chemicals provide numerous benefits, there is no doubt that some have potential to damage the environment and health. Toxicity must be evaluated and use must be carefully controlled and monitored in order to minimize potential damage. DNA microarray technology has become an important new technique in toxicology. We are using the yeast Saccharomyces cerevisiae as a model organism for toxicological study because it is a simple, fast-growing eukaryote that has been thoroughly characterized. In order to evaluate toxicity by newly synthesized or mixture chemicals, toxicity-induced gene expression alteration profiles by known chemicals should be collected. In our study, cells need to be exposed with same experimental cellular condition, semi lethal (IC50), respectively. In the case of o-nitrophenol (CAS; 88-75-5), the exposure dose was decided as 3 mM by growth curve with continuously diluted exposure. o-Nitrophenol is one of the nitrogen compounds, and 2-nitrophenol is reported to be less toxic than 4-. This substrate is suspected to be cardiovascular or blood toxicant, neurotoxicant. Keywords: stress response

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RNA-seq of C18-4 and TM4 cells samples from different M5 receptor modification groups

Project description:The goat of this project is to explore M5 receptor regulation spermatogenesis. We tried to search the mechanism of M5 receptor regulation spermatogenesis. RNA-seq of C18-4 and TM4 cells samples from different groups: C3NC, M5 knockdown in C18-4, TM3NC, M5 knockdown in TM4 cells. The cell were transfected with virus with inhibition of M5 expression ( M5 gene knockdown).

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Nitrophenol (p-nitrophenol) treatment with 1.5 mM for 2 h

Project description:The number and type of synthetic chemicals that are being produced worldwide continues to increase significantly. While these industrial chemicals provide numerous benefits, there is no doubt that some have potential to damage the environment and health. Toxicity must be evaluated and use must be carefully controlled and monitored in order to minimize potential damage. DNA microarray technology has become an important new technique in toxicology. We are using the yeast Saccharomyces cerevisiae as a model organism for toxicological study because it is a simple, fast-growing eukaryote that has been thoroughly characterized. In order to evaluate toxicity by newly synthesized or mixture chemicals, toxicity-induced gene expression alteration profiles by known chemicals should be collected. In our study, cells need to be exposed with same experimental cellular condition, semi lethal (IC50), respectively. In the case of p-nitrophenol (CAS; 100-02-7), the exposure dose was decided as 1.5 mM by growth curve with continuously diluted exposure. p-Nitrophenol is one of the nitrogen compounds, and 4-nitrophenol is reported to be more toxic than 2-. This substrate is reported to cause methemoglobinemia and suspected to be cardiovascular or blood toxicant, neurotoxicant, skin or sense organ toxicant. Keywords: stress response

2007-11-01 | GSE9190 | GEO

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