Kim S, Dugail I, Standridge M, Claycombe K, Chun J, Moustaïd-Moussa N
University of Tennessee, Nutrition Department and Agricultural Experiment Station, 1215 West Cumberland Avenue, Knoxville, TN 37996-1900, USA.
Biochem J. 2001 Aug 1;357(Pt 3):899-904. doi: 10.1042/0264-6021:3570899.
We have previously shown that angiotensin II (Ang II) increases the expression of the gene encoding adipocyte fatty acid synthase (FAS). Here we investigate the mechanism responsible for increased FAS gene transcription by Ang II. We demonstrate that Ang II increased luciferase activity by 3-fold in 3T3-L1 adipocytes transfected with fusion constructs linking the FAS promoter to the luciferase reporter gene. Interestingly, we mapped the Ang II regulatory sequences to the insulin-responsive region (E box) in the proximal FAS promoter. The E box alone was able to mediate Ang II responsiveness when linked to a heterologous promoter. However, this response was lost when mutations that abolished the binding of the E box to its transcription factors were introduced. Using adenoviral overexpression of a dominant-negative form of adipocyte determination and differentiation factor 1 (ADD1), a transcription factor that binds to the insulin-responsive E box, we demonstrated that ADD1 was required for Ang II regulation of the FAS gene in 3T3-L1 adipocytes. Furthermore, ADD1 expression was also up-regulated by Ang II. With the use of transfections as well as glucose transport assays, we further demonstrated that Ang II stimulation of the FAS gene was dependent on glucose. In conclusion, this is the first report that Ang II regulates adipocyte FAS gene transcription via insulin response sequences in a glucose-dependent manner and that this regulation is mediated at least in part via the ADD1 transcription factor.
我们之前已经表明,血管紧张素II(Ang II)可增加编码脂肪细胞脂肪酸合酶(FAS)的基因的表达。在此,我们研究Ang II导致FAS基因转录增加的机制。我们证明,在用连接FAS启动子与荧光素酶报告基因的融合构建体转染的3T3-L1脂肪细胞中,Ang II可使荧光素酶活性增加3倍。有趣的是,我们将Ang II调控序列定位到近端FAS启动子中的胰岛素反应区域(E盒)。当与异源启动子相连时,单独的E盒能够介导Ang II反应性。然而,当引入消除E盒与其转录因子结合的突变时,这种反应就消失了。通过腺病毒过表达脂肪细胞决定和分化因子1(ADD1)的显性负性形式(一种与胰岛素反应性E盒结合的转录因子),我们证明ADD1是3T3-L1脂肪细胞中Ang II对FAS基因调控所必需的。此外,Ang II也上调ADD1的表达。通过转染以及葡萄糖转运测定,我们进一步证明Ang II对FAS基因的刺激依赖于葡萄糖。总之,这是第一份报告,表明Ang II通过胰岛素反应序列以葡萄糖依赖的方式调节脂肪细胞FAS基因转录,并且这种调节至少部分是通过ADD1转录因子介导的。