Olsen Hanne, Haldosén Lars-Arne
Department of Medical Nutrition, Karolinska Institutet, NOVUM, S-141 86 Huddinge, Sweden.
Exp Cell Res. 2006 May 1;312(8):1371-80. doi: 10.1016/j.yexcr.2005.12.023. Epub 2006 Feb 2.
Signal transducer and activator of transcription 5A (STAT5A) has been shown to be important for terminal differentiation of mammary epithelial cells. In order to understand regulation of expression of STAT5A, the 5' end of the mouse Stat5a gene was isolated. Putative regulatory elements was searched for and several peroxisome proliferator response elements (PPREs) were found, one with high (12/13 nucleotides) and three with less (8-10/13) similarity to the reported consensus sequence. Mouse mammary epithelial HC11 cells were treated with peroxisome proliferator-activated receptor gamma (PPARgamma) ligand, the thiazolidinedione (TZD) troglitazone, and an increase in STAT5A protein expression was seen. The 5' flank of Stat5a gene was cloned in a luciferase reporter vector. A concentration dependent activation of the STAT5A-luciferase reporter was detected, when transiently transfected HC11 cells were treated with TZD. The activation could be inhibited by treatment with a PPARgamma antagonist. It has earlier been shown that epidermal growth factor (EGF) induces MAPK phosphorylation of PPARgamma resulting in a less transcriptionally active receptor. In HC11 cells, EGF inhibited TZD induced STAT5A-reporter activity suggesting that our previously reported EGF-mediated suppression of STAT5A expression is mediated in all or partly through inhibition of PPARgamma activity. Furthermore, the MEK inhibitor PD98059 inhibited the EGF effect. All together, data presented suggest that PPARgamma participates in regulation of STAT5A expression.
信号转导及转录激活因子5A(STAT5A)已被证明对乳腺上皮细胞的终末分化很重要。为了了解STAT5A表达的调控机制,分离了小鼠Stat5a基因的5'端。搜索了潜在的调控元件,发现了几个过氧化物酶体增殖物反应元件(PPREs),其中一个与报道的共有序列具有高度相似性(12/13个核苷酸),另外三个相似性较低(8 - 10/13个核苷酸)。用噻唑烷二酮(TZD)曲格列酮(过氧化物酶体增殖物激活受体γ(PPARγ)配体)处理小鼠乳腺上皮HC11细胞,发现STAT5A蛋白表达增加。将Stat5a基因的5'侧翼克隆到荧光素酶报告载体中。当用TZD处理瞬时转染的HC11细胞时,检测到STAT5A - 荧光素酶报告基因的浓度依赖性激活。用PPARγ拮抗剂处理可抑制这种激活。先前已经表明表皮生长因子(EGF)诱导PPARγ的MAPK磷酸化,导致受体转录活性降低。在HC11细胞中,EGF抑制TZD诱导的STAT5A报告基因活性,这表明我们先前报道的EGF介导的STAT5A表达抑制全部或部分是通过抑制PPARγ活性介导的。此外,MEK抑制剂PD98059抑制了EGF的作用。总之,所呈现的数据表明PPARγ参与了STAT5A表达的调控。