Jensen Ellis B, Zheng Donghai, Russell Robert A, Bassel-Duby Rhonda, Williams R Sanders, Olson Ann Louise, Dohm G Lynis
Department of Biology, Viterbo University, La Crosse, Wisconsin, USA.
Am J Physiol Regul Integr Comp Physiol. 2009 Jun;296(6):R1820-8. doi: 10.1152/ajpregu.90651.2008. Epub 2009 Mar 25.
Denervation by sciatic nerve resection causes decreased muscle glucose transporter 4 (GLUT4) expression, but little is known about the signaling events that cause this decrease. Experiments were designed to test the hypothesis that decreased GLUT4 expression in denervated muscle occurs because of decreased calcium/CaMK activity, which would then lead to decreased activation of the transcription factors myocyte enhancer factor 2 (MEF2) and GLUT4 enhancer factor (GEF), which are required for normal GLUT4 expression. GLUT4 mRNA was elevated in mice expressing constitutively active CaMK isoform IV (CaMKIV) and decreased by denervation. Denervation decreased GEF binding to the promoter and the content of GEF in the nucleus, but there was no change in either MEF2 binding or MEF2 protein content. Expression of a MEF2-dependent reporter gene did not change in denervated skeletal muscle. To determine the domains of the GLUT4 promoter that respond to denervation, transgenic mice expressing the chloramphenicol acetyl transferase (CAT) reporter gene driven by different lengths of the human GLUT4 promoter were denervated. Using several different promoter/reporter gene constructs, we found that all areas of the GLUT4 promoter were truncated or missing, except for the MEF2 binding domain and the basal promoter. All of the GLUT4 promoter/CAT reporter constructs evaluated responded normally to denervation. Our data lead us to conclude that decreased CaMK activity is not the reason for decreased GLUT4 content in denervated muscle and that negative control of GLUT4 expression is not mediated through the MEF2 or GEF-binding domains. These findings indicate that withdrawal of a GEF- or MEF2-dependent signal is not likely a major determinant of the denervation effect on GLUT4 expression. Thus, the response to denervation may be mediated by other elements present in the basal promoter of the GLUT4 gene.
坐骨神经切除导致去神经支配,会使肌肉中葡萄糖转运蛋白4(GLUT4)的表达降低,但对于导致这种降低的信号传导事件却知之甚少。本实验旨在验证以下假设:去神经支配的肌肉中GLUT4表达降低是由于钙/CaMK活性降低所致,进而导致正常GLUT4表达所需的转录因子肌细胞增强因子2(MEF2)和GLUT4增强因子(GEF)的激活减少。在组成型活性CaMK同工型IV(CaMKIV)表达的小鼠中,GLUT4 mRNA升高,而去神经支配则使其降低。去神经支配降低了GEF与启动子的结合以及细胞核中GEF的含量,但MEF2的结合或MEF2蛋白含量均无变化。在去神经支配的骨骼肌中,MEF2依赖性报告基因的表达没有改变。为了确定GLUT4启动子中对去神经支配有反应的结构域,对表达由不同长度的人GLUT4启动子驱动的氯霉素乙酰转移酶(CAT)报告基因的转基因小鼠进行去神经支配。使用几种不同的启动子/报告基因构建体,我们发现除了MEF2结合结构域和基础启动子外,GLUT4启动子的所有区域均被截断或缺失。所有评估的GLUT4启动子/CAT报告构建体对去神经支配的反应均正常。我们的数据使我们得出结论,CaMK活性降低不是去神经支配肌肉中GLUT4含量降低的原因,并且GLUT4表达的负调控不是通过MEF2或GEF结合结构域介导的。这些发现表明,GEF或MEF2依赖性信号的缺失不太可能是去神经支配对GLUT4表达影响的主要决定因素。因此,对去神经支配的反应可能由GLUT4基因基础启动子中存在的其他元件介导。