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Sökning: WFRF:(Hermanson O) > (2015-2019) > Tet3 mediates stabl...

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FältnamnIndikatorerMetadata
00002679naa a2200361 4500
001oai:prod.swepub.kib.ki.se:131541902
003SwePub
008240701s2015 | |||||||||||000 ||eng|
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1315419022 URI
024a https://doi.org/10.1038/cddis.2015.1592 DOI
040 a (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Bose, R4 aut
2451 0a Tet3 mediates stable glucocorticoid-induced alterations in DNA methylation and Dnmt3a/Dkk1 expression in neural progenitors
264 c 2015-06-18
264 1b Springer Science and Business Media LLC,c 2015
520 a Developmental exposure to excess glucocorticoids (GCs) has harmful neurodevelopmental effects, which include persistent alterations in the differentiation potential of embryonic neural stem cells (NSCs). The mechanisms, however, are largely unknown. Here, we investigated the effects of dexamethasone (Dex, a synthetic GC analog) by MeDIP-like genome-wide analysis of differentially methylated DNA regions (DMRs) in NSCs isolated from embryonic rat cortices. We found that Dex-induced genome-wide DNA hypomethylation in the NSCs in vitro. Similarly, in utero exposure to Dex resulted in global DNA hypomethylation in the cerebral cortex of 3-day-old mouse pups. Dex-exposed NSCs displayed stable changes in the expression of the DNA methyltransferase Dnmt3a, and Dkk1, an essential factor for neuronal differentiation. These alterations were dependent on Tet3 upregulation. In conclusion, we propose that GCs elicit strong and persistent effects on DNA methylation in NSCs with Tet3 playing an essential role in the regulation of Dnmt3a and Dkk1. Noteworthy is the occurrence of similar changes in Dnmt3a and Dkk1 gene expression after exposure to excess GC in vivo.
700a Spulber, Su Karolinska Institutet4 aut
700a Kilian, P4 aut
700a Heldring, Nu Karolinska Institutet4 aut
700a Lonnerberg, Pu Karolinska Institutet4 aut
700a Johnsson, Au Karolinska Institutet4 aut
700a Conti, Mu Karolinska Institutet4 aut
700a Hermanson, Ou Karolinska Institutet4 aut
700a Ceccatelli, Su Karolinska Institutet4 aut
710a Karolinska Institutet4 org
773t Cell death & diseased : Springer Science and Business Media LLCg 6, s. e1793-q 6<e1793-x 2041-4889
856u https://www.nature.com/articles/cddis2015159.pdf
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:131541902
8564 8u https://doi.org/10.1038/cddis.2015.159

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