Son Young June, Hur Min Kyu, Ryu Byung Jun, Park Sang Kyu, Damante Giuseppe, D'Elia Angela Valentina, Costa Maria E, Ojeda Sergio R, Lee Byung Ju
Department of Biological Sciences, College of Natural Sciences, University of Ulsan, Ulsan 680-749, South Korea.
J Biol Chem. 2003 Jul 18;278(29):27043-52. doi: 10.1074/jbc.M303157200. Epub 2003 May 2.
In recent years, it has become increasingly evident that angiotensins synthesized in the brain contribute to regulating body fluid homeostasis. Although angiotensinogen, the unique angiotensin precursor, is produced in the brain, the factors that regulate its gene expression remain unknown. We recently found that TTF-1, a homeodomain-containing transcription factor essential for the development of the fetal diencephalon, is postnatally expressed in discrete areas of the hypothalamus. We now report that the subfornical organ, an important site of angiotensinogen synthesis, is an extra-hypothalamic site of TTF-1 expression. Double in situ hybridization histochemistry demonstrated the presence of TTF-1 mRNA in angiotensinogen-producing cells of the rat subfornical organ. RNase protection assays showed that TTF-1 and angiotensinogen mRNA levels are simultaneously increased in the subfornical organ by water deprivation. The angiotensinogen promoter contains seven presumptive TTF-1 binding motifs, four of which are recognized by the TTF-1 homeodomain. In the C6 glioma cell line, TTF-1 transactivates the angiotensinogen promoter in a dose-dependent manner. This transactivation is abolished by deletion of the TTF-1 binding motif at -125. Intracranial administration of an antisense TTF-1 oligodeoxynucleotide decreased angiotensinogen mRNA in the subfornical organ and dramatically reduced the animal's water intake while increasing urine excretion. Moreover, plasma arginine vasopressin content was decreased by the same treatment. These results demonstrate a novel role for TTF-1 in the regulation of body fluid homeostasis, exerted via the transactivational control of angiotensinogen synthesis in the subfornical organ.
近年来,越来越明显的是,大脑中合成的血管紧张素有助于调节体液平衡。尽管血管紧张素原是唯一的血管紧张素前体,在大脑中产生,但其基因表达的调节因子仍不清楚。我们最近发现,TTF-1是一种含同源结构域的转录因子,对胎儿间脑的发育至关重要,在出生后在下丘脑的离散区域表达。我们现在报告,穹窿下器是血管紧张素原合成的重要部位,是TTF-1表达的下丘脑外部位。双重原位杂交组织化学显示大鼠穹窿下器产生血管紧张素原的细胞中存在TTF-1 mRNA。核糖核酸酶保护试验表明,脱水可使穹窿下器中TTF-1和血管紧张素原mRNA水平同时升高。血管紧张素原启动子包含七个推定的TTF-1结合基序,其中四个可被TTF-1同源结构域识别。在C6胶质瘤细胞系中,TTF-1以剂量依赖的方式反式激活血管紧张素原启动子。通过缺失-125处的TTF-1结合基序,这种反式激活被消除。颅内注射反义TTF-1寡脱氧核苷酸可降低穹窿下器中血管紧张素原mRNA水平,并显著减少动物的饮水量,同时增加尿量。此外,相同处理可降低血浆精氨酸加压素含量。这些结果表明TTF-1在调节体液平衡中具有新的作用,通过对穹窿下器中血管紧张素原合成的反式激活控制来发挥作用。