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Evaluation of mRNA ...
Evaluation of mRNA markers in differentiating human SH-SY5Y cells for estimation of developmental neurotoxicity
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- Hinojosa, M. G. (author)
- Stockholm Univ, Dept Biochem & Biophys, S-10691 Stockholm, Sweden.
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- Johansson, Y. (author)
- Stockholm Univ, Dept Biochem & Biophys, S-10691 Stockholm, Sweden.
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- Cediel Ulloa, Andrea (author)
- Uppsala universitet,Fysiologi och miljötoxikologi
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- Ivanova, E. (author)
- Stockholm Univ, Dept Biochem & Biophys, S-10691 Stockholm, Sweden.
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- Gabring, N. (author)
- Stockholm Univ, Dept Biochem & Biophys, S-10691 Stockholm, Sweden.
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- Gliga, A. (author)
- Karolinska Institutet
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- Forsby, A. (author)
- Stockholm Univ, Dept Biochem & Biophys, S-10691 Stockholm, Sweden.
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Stockholm Univ, Dept Biochem & Biophys, S-10691 Stockholm, Sweden Fysiologi och miljötoxikologi (creator_code:org_t)
- Elsevier, 2023
- 2023
- English.
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In: Neurotoxicology. - : Elsevier. - 0161-813X .- 1872-9711. ; 97, s. 65-77
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Abstract
Subject headings
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- Current guidelines for developmental neurotoxicity (DNT) evaluation are based on animal models. These have limitations so more relevant, efficient and robust approaches for DNT assessment are needed. We have used the human SH-SY5Y neuroblastoma cell model to evaluate a panel of 93 mRNA markers that are frequent in Neuronal diseases and functional annotations and also differentially expressed during retinoic acid-induced differentiation in the cell model. Rotenone, valproic acid (VPA), acrylamide (ACR) and methylmercury chlo-ride (MeHg) were used as DNT positive compounds. Tolbutamide, D-mannitol and clofibrate were used as DNT negative compounds. To determine concentrations for exposure for gene expression analysis, we developed a pipeline for neurite outgrowth assessment by live-cell imaging. In addition, cell viability was measured by the resazurin assay. Gene expression was analyzed by RT-qPCR after 6 days of exposure during differentiation to concentrations of the DNT positive compounds that affected neurite outgrowth, but with no or minimal effect on cell viability. Methylmercury affected cell viability at lower concentrations than neurite outgrowth, hence the cells were exposed with the highest non-cytotoxic concentration. Rotenone (7.3 nM) induced 32 differentially expressed genes (DEGs), ACR (70 mu M) 8 DEGs, and VPA (75 mu M) 16 DEGs. No individual genes were significantly dysregulated by all 3 DNT positive compounds (p < 0.05), but 9 genes were differentially expressed by 2 of them. Methylmercury (0.8 nM) was used to validate the 9 DEGs. The expression of SEMA5A (encoding semaphorin 5A) and CHRNA7 (encoding nicotinic acetylcholine receptor subunit alpha 7) was downregulated by all 4 DNT positive compounds. None of the DNT negative compounds dysregulated any of the 9 DEGs in common for the DNT positive compounds. We suggest that SEMA5A or CHRNA7 should be further evaluated as biomarkers for DNT studies in vitro since they also are involved in neurodevelopmental adverse outcomes in humans.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
- NATURVETENSKAP -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
- NATURAL SCIENCES -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
Keyword
- Developmental neurotoxicity
- in vitro
- mRNA markers
- Live-cell imaging
- Neurite outgrowth
Publication and Content Type
- ref (subject category)
- art (subject category)
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