From transient transcriptome responses to disturbed neurodevelopment : role of histone acetylation and methylation as epigenetic switch between reversible and irreversible drug effects

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2014
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Rempel, Eugen
Kolde, Raivo
Meganathan, Kesavan
Henry, Margit
Sachinidis, Agapios
Hengstler, Jan G.
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Archives of toxicology. 2014, 88(7), pp. 1451-1468. ISSN 0340-5761. eISSN 1432-0738. Available under: doi: 10.1007/s00204-014-1279-6
Zusammenfassung

The superordinate principles governing the transcriptome response of differentiating cells exposed to drugs are still unclear. Often, it is assumed that toxicogenomics data reflect the immediate mode of action (MoA) of drugs. Alternatively, transcriptome changes could describe altered differentiation states as indirect consequence of drug exposure. We used here the developmental toxicants valproate and trichostatin A to address this question. Neurally differentiating human embryonic stem cells were treated for 6 days. Histone acetylation (primary MoA) increased quickly and returned to baseline after 48 h. Histone H3 lysine methylation at the promoter of the neurodevelopmental regulators PAX6 or OTX2 was increasingly altered over time. Methylation changes remained persistent and correlated with neurodevelopmental defects and with effects on PAX6 gene expression, also when the drug was washed out after 3-4 days. We hypothesized that drug exposures altering only acetylation would lead to reversible transcriptome changes (indicating MoA), and challenges that altered methylation would lead to irreversible developmental disturbances. Data from pulse-chase experiments corroborated this assumption. Short drug treatment triggered reversible transcriptome changes; longer exposure disrupted neurodevelopment. The disturbed differentiation was reflected by an altered transcriptome pattern, and the observed changes were similar when the drug was washed out during the last 48 h. We conclude that transcriptome data after prolonged chemical stress of differentiating cells mainly reflect the altered developmental stage of the model system and not the drug MoA. We suggest that brief exposures, followed by immediate analysis, are more suitable for information on immediate drug responses and the toxicity MoA.

Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
570 Biowissenschaften, Biologie
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Valproic acid, Embryonic stem cell, Histone deacetylase, Developmental toxicity, Histone modification
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ISO 690STIEGLER, Nina, Stefanie KLIMA, Eugen REMPEL, Violeta IVANOVA-ROHLING, Raivo KOLDE, Matthias K. WENG, Kesavan MEGANATHAN, Margit HENRY, Agapios SACHINIDIS, Jan G. HENGSTLER, Michael R. BERTHOLD, Jörg RAHNENFÜHRER, Tanja WALDMANN, Marcel LEIST, 2014. From transient transcriptome responses to disturbed neurodevelopment : role of histone acetylation and methylation as epigenetic switch between reversible and irreversible drug effects. In: Archives of toxicology. 2014, 88(7), pp. 1451-1468. ISSN 0340-5761. eISSN 1432-0738. Available under: doi: 10.1007/s00204-014-1279-6
BibTex
@article{Stiegler2014trans-29398,
  year={2014},
  doi={10.1007/s00204-014-1279-6},
  title={From transient transcriptome responses to disturbed neurodevelopment : role of histone acetylation and methylation as epigenetic switch between reversible and irreversible drug effects},
  number={7},
  volume={88},
  issn={0340-5761},
  journal={Archives of toxicology},
  pages={1451--1468},
  author={Stiegler, Nina and Klima, Stefanie and Rempel, Eugen and Ivanova-Rohling, Violeta and Kolde, Raivo and Weng, Matthias K. and Meganathan, Kesavan and Henry, Margit and Sachinidis, Agapios and Hengstler, Jan G. and Berthold, Michael R. and Rahnenführer, Jörg and Waldmann, Tanja and Leist, Marcel}
}
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