Our recent study demonstrated that constitutively activated RelB/NF-kappa B2 positively regulates the CRH in the human placenta. In the current study, we explored the role of the glucocorticoid receptor (GR) signaling in constitutive activation of the noncanonical NF-kappa B pathway. A glucocorticoid response element (GRE) motif search suggests that both NF-kappa B inducing kinase (NIK) and RelB genes, which are key regulators of the noncanonical NF-kappa B pathway, have a putative GRE within their promoter, approximately 1 kb upstream from the transcription start site. By using chromatin immunoprecipitation assay we identified that the GR and phosphorylated GR at Ser211 were associated with the GREs of both NIK and RelB. Dexamethasone stimulated expression of NIK, RelB, NF-kappa B2 as well as CRH and cyclooxygenase-2 (COX-2). Repression of GR by short interfering RNA resulted in inhibition of NIK, RelB, NF-kappa B2, CRH, and COX-2. In addition, depletion of GR attenuated glucocorticoid-mediated up-regulation of NIK, RelB, NF-kappa B2, CRH, and COX-2. Furthermore, siRNA specifically targeting NIK down-regulated CRH and COX-2. Taken together, these results suggest that constitutive activation of the noncanonical NF-kappa B pathway in term human placenta is driven by the GR signaling, which in turn up-regulates placental CRH and other NF-kappa B-responsive genes. (Molecular Endocrinology 27: 203-211, 2013)
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据