| Literature DB >> 24966332 |
Ilkka Paatero1, Tiffany N Seagroves2, Katri Vaparanta3, Wen Han4, Frank E Jones4, Randall S Johnson5, Klaus Elenius6.
Abstract
Conditional knock-out of Hif1a in the mouse mammary gland impairs lobuloalveolar differentiation during lactation. Here, we demonstrate that expression of ErbB4 was reduced in the lobulalveoli of mice with mammary gland-specific deletion of Hif1a. Erbb4 was not, however, a direct target gene for transcriptional regulation by HIF-1α in vitro. HIF-1α overexpression or HIF accumulating prolyl hydroxylase inhibitors reduced ErbB4 endocytosis, promoted transcriptional co-regulatory activity of ErbB4, and stimulated ErbB4-induced differentiation of mammary carcinoma cells. Consistently, RNA interference-mediated down-regulation of HIF-1α resulted in reduced ErbB4 protein amount and reduced mammary carcinoma cell differentiation. These findings indicate that HIF-1α is a physiologically relevant regulator of ErbB4 and that ErbB4 is involved in HIF-regulated differentiation of the mammary gland.Entities:
Keywords: Cell Signaling; Epidermal Growth Factor Receptor (EGFR); ErbB4; Growth Factor; Hypoxia-inducible Factor (HIF); Lactation; Mammary Gland; Receptor Tyrosine Kinase; Signal Transduction
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Year: 2014 PMID: 24966332 PMCID: PMC4139252 DOI: 10.1074/jbc.M113.533497
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157