Evidence map›Paper›PMID 25181051›Full record

ArticlePloS one2014

Exposure to low-dose bisphenol A impairs meiosis in the rat seminiferous tubule culture model: a physiotoxicogenomic approach.

Sazan Ali, Gérard Steinmetz, Guillaume Montillet, Marie-Hélène Perrard, Anderson Loundou, Philippe Durand, Marie-Roberte Guichaoua, Odette Prat

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sazan AliInstitut Méditerranéen de Biodiversité et d'Ecologie marine et continentale (IMBE), Centre National de la Recherche Scientifique (CNRS) UMR 7263/ Institut de Recherche pour le Développement (IRD) 237, Faculté de Médecine, Aix-Marseille Université (AMU), Marseille, France.
Gérard SteinmetzInstitute of Environmental Biology and Biotechnology (IBEB), Life Science division, French Alternative Energy and Atomic Energy Commission (CEA), Marcoule, Bagnols-sur-Cèze, France.
Guillaume MontilletInstitut de Génomique Fonctionnelle de Lyon (IGFL), Centre National de la Recherche Scientifique (CNRS) UMR 5242/ Institut National de la Recherche Agronomique (INRA), Ecole Normale Supérieure de Lyon (ENS), Lyon, France.
Marie-Hélène PerrardInstitut de Génomique Fonctionnelle de Lyon (IGFL), Centre National de la Recherche Scientifique (CNRS) UMR 5242/ Institut National de la Recherche Agronomique (INRA), Ecole Normale Supérieure de Lyon (ENS), Lyon, France.
Anderson LoundouUnité d'Aide Méthodologique à la Recherche clinique, Faculté de Médecine, Aix-Marseille Université (AMU), Marseille, France.
Philippe DurandInstitut de Génomique Fonctionnelle de Lyon (IGFL), Centre National de la Recherche Scientifique (CNRS) UMR 5242/ Institut National de la Recherche Agronomique (INRA), Ecole Normale Supérieure de Lyon (ENS), Lyon, France.
Marie-Roberte GuichaouaInstitut Méditerranéen de Biodiversité et d'Ecologie marine et continentale (IMBE), Centre National de la Recherche Scientifique (CNRS) UMR 7263/ Institut de Recherche pour le Développement (IRD) 237, Faculté de Médecine, Aix-Marseille Université (AMU), Marseille, France.
Odette PratInstitute of Environmental Biology and Biotechnology (IBEB), Life Science division, French Alternative Energy and Atomic Energy Commission (CEA), Marcoule, Bagnols-sur-Cèze, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBisphenol A (BPA) is one of the most widespread chemicals in the world and is suspected of being responsible for male reproductive impairments. Nevertheless, its molecular mode of action on spermatogenesis is unclear. This work combines physiology and toxicogenomics to identify mechanisms by which BPA affects the timing of meiosis and induces germ-cell abnormalities.

methodsWe used a rat seminiferous tubule culture model mimicking the in vivo adult rat situation. BPA (1 nM and 10 nM) was added to the culture medium. Transcriptomic and meiotic studies were performed on the same cultures at the same exposure times (days 8, 14, and 21). Transcriptomics was performed using pangenomic rat microarrays. Immunocytochemistry was conducted with an anti-SCP3 antibody.

resultsThe gene expression analysis showed that the total number of differentially expressed transcripts was time but not dose dependent. We focused on 120 genes directly involved in the first meiotic prophase, sustaining immunocytochemistry. Sixty-two genes were directly involved in pairing and recombination, some of them with high fold changes. Immunocytochemistry indicated alteration of meiotic progression in the presence of BPA, with increased leptotene and decreased diplotene spermatocyte percentages and partial meiotic arrest at the pachytene checkpoint. Morphological abnormalities were observed at all stages of the meiotic prophase. The prevalent abnormalities were total asynapsis and apoptosis. Transcriptomic analysis sustained immunocytological observations.

conclusionWe showed that low doses of BPA alter numerous genes expression, especially those involved in the reproductive system, and severely impair crucial events of the meiotic prophase leading to partial arrest of meiosis in rat seminiferous tubule cultures.

Indexed as

Models, BiologicalToxicogeneticsAnimalsBenzhydryl CompoundsBisphenol A CompoundsCell NucleusCells, CulturedDown-RegulationGene Expression ProfilingMaleMeiosisOligonucleotide Array Sequence AnalysisPhenolsRats, Sprague-DawleyRecombination, GeneticReproducibility of ResultsBenzhydryl Compoundsbisphenol ABisphenol A CompoundsPhenols

Identifiers

PMID25181051
PMCPMC4152015

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.