4.7 Article

Non-Lethal Concentration of MeHg Causes Marked Responses in the DNA Repair, Integrity, and Replication Pathways in the Exposed Human Salivary Gland Cell Line

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FRONTIERS IN PHARMACOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.698671

关键词

toxicology; salivary gland; transcriptome; methylmercury; biomarker

资金

  1. Brazilian National Council for Scientific and Technological Development (CNPq)
  2. Brazilian Government/Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [001]
  3. Programa Nacional de Pos Doutorado/Capes (PNPD/CAPES)
  4. Pro-Reitoria de Pesquisa e Pos-graduacao da Universidade Federal do Para (PROPESP-UFPA)

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The study aims to investigate the gene expression changes in human salivary gland cells after exposure to MeHg through transcriptome analysis. The results showed that MeHg altered the expression of 155 genes, with upregulated genes mainly related to cell-cycle progression, DNA repair, and GSH basal metabolism, while downregulated genes were associated with impaired cell metabolism.
In Brazilian northern Amazon, communities are potentially exposed and vulnerable to methylmercury (MeHg) toxicity through the vast ingestion of fish. In vivo and in vitro studies demonstrated that the salivary glands as a susceptible organ to this potent environmental pollutant, reporting alterations on physiological, biochemical, and proteomic parameters. However, the alterations caused by MeHg on the gene expression of the exposed human salivary gland cells are still unknown. Therefore, the goal was to perform the transcriptome profile of the human salivary gland cell line after exposure to MeHg, using the microarray technique and posterior bioinformatics analysis. The cell exposure was performed using 2.5 mu M MeHg. A previously published study demonstrated that this concentration belongs to a range of concentrations that caused biochemical and metabolic alterations in this linage. As a result, the MeHg exposure did not cause lethality in the human salivary gland cells line but was able to alter the expression of 155 genes. Downregulated genes (15) are entirety relating to the cell metabolism impairment, and according to KEGG analysis, they belong to the glycosphingolipid (GSL) biosynthesis pathway. On the other hand, most of the 140 upregulated genes were related to cell-cycle progression, DNA repair, and replication pathway, or cellular defenses through the GSH basal metabolism. These genomic changes revealed the effort to the cell to maintain physiological and genomic stability to avoid cell death, being in accordance with the nonlethality in the toxicity test. Last, the results support in-depth studies on nonlethal MeHg concentrations for biomarkers identification that interpret transcriptomics data in toxicological tests serving as an early alert of physiological changes in vitro biological models.

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