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Quantitative proteomic dataset of mouse caput epididymal epithelial cells exposed to acrylamide in vivo.


ABSTRACT: This article reports the proteomic legacy of in vivo exposure to the xenobiotic, acrylamide, on the epithelial cell population of the proximal segments of the mouse epididymis. Specifically, adult male mice were administered acrylamide (25 mg/kg bw/day) or vehicle control for five consecutive days before dissection of the epididymis. Epididymal epithelial cells were isolated from the proximal (caput) epididymal segment and subjected to quantitative proteomic analysis using multiplexed tandem mass tag (TMT) labeling coupled to mass spectrometry. Here, we report the data generated by this strategy, including the identification of 4405 caput epididymal epithelial cell proteins, approximately 6.8% of which displayed altered expression in response to acrylamide challenge. Our interpretation and discussion of these data features in the article "Acrylamide modulates the mouse epididymal proteome to drive alterations in the sperm small non-coding RNA profile and dysregulate embryo development".

SUBMITTER: Trigg NA 

PROVIDER: S-EPMC8980551 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Quantitative proteomic dataset of mouse caput epididymal epithelial cells exposed to acrylamide <i>in vivo</i>.

Trigg Natalie A NA   Skerrett-Byrne David A DA   Martin Jacinta H JH   De Iuliis Geoffry N GN   Dun Matthew D MD   Roman Shaun D SD   Eamens Andrew L AL   Nixon Brett B  

Data in brief 20220308


This article reports the proteomic legacy of <i>in vivo</i> exposure to the xenobiotic, acrylamide, on the epithelial cell population of the proximal segments of the mouse epididymis. Specifically, adult male mice were administered acrylamide (25 mg/kg bw/day) or vehicle control for five consecutive days before dissection of the epididymis. Epididymal epithelial cells were isolated from the proximal (caput) epididymal segment and subjected to quantitative proteomic analysis using multiplexed tan  ...[more]

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