| Literature DB >> 27259582 |
Luke Forster1,2, Jill Finlayson1,2, Reza Ghassemifar3,4,5.
Abstract
Beta (β)-thalassaemic erythroblasts grown in vitro have reduced nuclear factor kappa B (NF-κB) pathway gene expression. By inhibiting this pathway in erythroblasts from normal individuals, important downstream genes affected by this inhibition can be identified. Bay 11-7082 is a potent inhibitor of the NF-κB pathway, it acts irreversibly, inhibiting NF-κB activation by blocking tumor necrosis factor alpha (TNF-α)-induced phosphorylation of the inhibitory IκB subunit thereby preventing NF-κB activation. In this study, hematopoietic stem cells were isolated from the peripheral blood of 6 healthy individuals and were then cultured for 14 days in conditions which promote erythroid differentiation. Following erythroid lineage enrichment, these cells were stimulated with TNFα or inhibited with Bay 11-7082. Subsequent RNA isolation and gene expression analyses were performed using pooled cDNA with custom PCR arrays. Genes of interest were examined individually on non-pooled samples. Our data identified RNF187, a RING finger domain gene as being downregulated in response to NF-κB inhibition.Entities:
Keywords: Erythropoiesis; Gene expression; NF-κB; Quantitative real time PCR
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Year: 2016 PMID: 27259582 DOI: 10.1007/s10528-016-9750-0
Source DB: PubMed Journal: Biochem Genet ISSN: 0006-2928 Impact factor: 1.890