Gerhard M, Neumayer N, Presecan-Siedel E, Zanner R, Lengyel E, Cramer T, Höcker M, Prinz C
II Medizinische Klinik, Technical University, D-81675 Munich, Germany.
Endocrinology. 2001 Aug;142(8):3663-72. doi: 10.1210/endo.142.8.8311.
Gastric enterochromaffin-like cells produce histamine in response to the antral hormone gastrin and accumulate the biogenic amine in secretory organelles via vesicular monoamine transporter subtype 2. The putative effects of gastrin on vesicular monoamine transporter subtype 2 expression and promoter activity are poorly understood. In the present study we used highly enriched rat enterochromaffin-like cells (purity, >90%) and rat pheochromocytoma cells stably transfected with a gastrin/cholecystokinin B receptor to investigate the expression and transcriptional regulation of vesicular monoamine transporter subtype 2. Stimulation of vesicular monoamine transporter subtype 2 mRNA and protein expression was observed in isolated enterochromaffin-like cells after 3- to 7-h incubation with gastrin (10(-7) M), forskolin (10(-5) M), or ionomycin (10(-5) M). Deletion analysis of the rat vesicular monoamine transporter subtype 2 promoter defined the minimal promoter sequence necessary for full basal activity as a -121 bp segment upstream of exon 1 containing two Sp1 sites (-97 to -88 bp and -68 to -59 bp) and a cAMP-responsive element (-44 to -35 bp). Gastrin (10(-7) M) stimulated extracellular signal related kinase1/2 phosphorylation, activated Sp1 and cAMP-responsive element-binding protein, and further induced activity of the complete rat vesicular monoamine transporter subtype 2 promoter (-800 bp) in gastrin/cholecystokinin B receptor cells. The -121-bp fragment was able to confer full gastrin responsiveness, and site-directed mutagenesis of the Sp1 and cAMP-responsive element motifs demonstrated their crucial importance for basal and inducible activities. Comparison of promoter activity of histidine decarboxylase, chromogranin A, or vesicular monoamine transporter subtype 2 in transfected cell lines revealed significant differences in basal and gastrin-stimulated activities. Our current study provides the first evidence that gastrin directly stimulates the expression and promoter activity of vesicular monoamine transporter subtype 2. Sp1 and cAMP-responsive element-binding protein recognition motifs located within 121 bp upstream of exon 1 appear to be indispensable for full basal and inducible promoter activities. Diverging effects of gastrin on histidine decarboxylase, chromogranin A, and vesicular monoamine transporter subtype 2 promoter may account for the coordinated synthesis and storage of histamine in this neuroendocrine cell type.
胃肠嗜铬样细胞在胃窦激素胃泌素的作用下产生组胺,并通过囊泡单胺转运体2亚型将生物胺积累在分泌细胞器中。胃泌素对囊泡单胺转运体2亚型表达和启动子活性的假定作用了解甚少。在本研究中,我们使用高度纯化的大鼠肠嗜铬样细胞(纯度>90%)和稳定转染胃泌素/缩胆囊素B受体的大鼠嗜铬细胞瘤细胞,来研究囊泡单胺转运体2亚型的表达和转录调控。在用胃泌素(10⁻⁷ M)、福斯可林(10⁻⁵ M)或离子霉素(10⁻⁵ M)孵育3至7小时后,在分离的肠嗜铬样细胞中观察到囊泡单胺转运体2 mRNA和蛋白质表达受到刺激。对大鼠囊泡单胺转运体2启动子的缺失分析确定了完整基础活性所需的最小启动子序列,为外显子1上游-121 bp的片段,包含两个Sp1位点(-97至-88 bp和-68至-59 bp)和一个cAMP反应元件(-44至-35 bp)。胃泌素(10⁻⁷ M)刺激细胞外信号相关激酶1/2磷酸化,激活Sp1和cAMP反应元件结合蛋白,并进一步诱导胃泌素/缩胆囊素B受体细胞中完整大鼠囊泡单胺转运体2启动子(-800 bp)的活性。-121 bp片段能够赋予完全的胃泌素反应性,对Sp1和cAMP反应元件基序的定点诱变证明了它们对基础活性和诱导活性的至关重要性。在转染细胞系中比较组氨酸脱羧酶、嗜铬粒蛋白A或囊泡单胺转运体2亚型的启动子活性,发现基础活性和胃泌素刺激活性存在显著差异。我们目前的研究提供了首个证据,表明胃泌素直接刺激囊泡单胺转运体2亚型的表达和启动子活性。位于外显子1上游121 bp内的Sp1和cAMP反应元件结合蛋白识别基序似乎是完全基础活性和诱导启动子活性所不可或缺的。胃泌素对组氨酸脱羧酶、嗜铬粒蛋白A和囊泡单胺转运体2启动子的不同作用,可能解释了这种神经内分泌细胞类型中组胺的协同合成和储存。