Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1021
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dc.contributor.authorGupta, Satish Kumar-
dc.contributor.authorMalhotra, Sudha Saryu-
dc.date.accessioned2018-05-23T09:01:08Z-
dc.date.available2018-05-23T09:01:08Z-
dc.date.issued2017-08-
dc.identifier.urihttp://hdl.handle.net/123456789/1021-
dc.description.abstractNur-77, a member of the NR4A sub-family of nuclear orphan receptors, is downregulated in the placentae of pre-eclamptic women. Here, we investigate the relevance of Nor-1, Nurr-1 and Nur-77 in trophoblastic cell differentiation. Their transcript levels were found to be significantly upregulated in BeWo cells treated with forskolin. The maximum increase was observed after 2 h, with a second peak in the expression levels after 48 h. The expression of NR4A sub-family members was also found to be upregulated in BeWo cells after treatment with hCG and GnRH. A similar significant increase was observed at the respective protein levels after 2 and 48 h of treatment with forskolin, hCG or GnRH. Silencing Nor-1, Nurr-1 or Nur-77 individually did not show any effect on forskolin-, hCG- and/or GnRH-mediated BeWo cell fusion and/or hCG secretion. After silencing any one member of the NR4A sub-family, an increase in the transcript levels of the other sub-family members was observed, indicating a compensatory effect due to their functional redundancy. Simultaneously silencing all three NR4A sub-family members significantly downregulated forskolin- and hCG-mediated BeWo cell fusion and/or hCG secretion. However, a considerable amount of cell death occurred after forskolin or hCG treatment as compared to the control siRNA-transfected cells. These results suggest that the NR4A sub-family of nuclear orphan receptors has a role in trophoblastic cell differentiation.en_US
dc.publisherBioMed Central Ltden_US
dc.titleRelevance of the NR4A sub-family of nuclear orphan receptors in trophoblastic BeWo cell differentiationen_US
dc.keywordGnRH; Nor-1; Nur-77; Nurr-1; Trophoblast differentiation; hCGen_US
dc.journalCellular & Molecular Biology Lettersen_US
dc.volumeno22en_US
dc.pages15en_US
Appears in Collections:Reproductive Cell Biology, Publications

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