Zingg H H, Lefebvre D, Almazan G
J Biol Chem. 1986 Oct 5;261(28):12956-9.
Although the steps involved in biosynthesis and secretion of the neuropeptide vasopressin (AVP) have been extensively studied, the factors which regulate AVP gene expression remain unknown. Therefore, we sought to determine the dynamics of AVP mRNA accumulation in response to a strong stimulus for AVP release, i.e. during salt imbibition and the ensuing period of rehydration. AVP mRNA levels were determined in terms of absolute amounts by a novel quantitative densitometric hybridization assay, using in vitro synthesized sense-strand RNA as a quantitative standard and complementary anti-sense RNA as a specific probe. The template used for RNA transcription consisted of a 196-base pair genomic DNA fragment corresponding to exon C of the rat AVP gene. Determination of basal hypothalamic AVP mRNA levels yielded 12.5 +/- 2.7 fmol/hypothalamus. Salt imbibition, which induced a 6% rise in blood osmolality and an 82% loss of pituitary AVP, resulted in a 3-fold increase of AVP mRNA to 35 +/- 5 fmol/hypothalamus. Following rehydration, plasma osmolality returned to control levels by day 2, pituitary AVP by day 6, and hypothalamic AVP by day 14. By contrast, AVP mRNA levels remained significantly elevated throughout the 30-day rehydration period. Furthermore, pituitary AVP reached a level of 177% of control by day 14 of rehydration. These data show that osmotic stimulation results in a long-lasting elevation of hypothalamic AVP mRNA; during rehydration, these elevated mRNA levels direct AVP biosynthesis at a rate which surpasses secretory demands; AVP mRNA accumulation does not appear to be directly regulated by either pituitary or hypothalamic AVP. Therefore, either an unusually long half-life of greater than or equal to 7 days must be assumed for AVP mRNA or, alternatively, a continued stimulation of AVP gene transcription must occur, even in the absence of a secretory stimulus and following complete repletion of cellular AVP stores.
尽管神经肽血管加压素(AVP)生物合成与分泌所涉及的步骤已得到广泛研究,但调节AVP基因表达的因素仍不清楚。因此,我们试图确定在强烈刺激AVP释放时,即盐摄取期间及随后的补液期,AVP mRNA积累的动态变化。通过一种新型的定量光密度杂交分析法,以体外合成的正义链RNA作为定量标准,互补反义RNA作为特异性探针,以绝对量来测定AVP mRNA水平。用于RNA转录的模板由一个196个碱基对的基因组DNA片段组成,该片段对应大鼠AVP基因的外显子C。测定下丘脑基础AVP mRNA水平,结果为12.5±2.7 fmol/下丘脑。盐摄取导致血液渗透压升高6%,垂体AVP损失82%,使AVP mRNA增加3倍,达到35±5 fmol/下丘脑。补液后,血浆渗透压在第2天恢复到对照水平,垂体AVP在第6天恢复,下丘脑AVP在第14天恢复。相比之下,在整个30天的补液期内,AVP mRNA水平仍显著升高。此外,补液第14天时,垂体AVP达到对照水平的177%。这些数据表明,渗透压刺激导致下丘脑AVP mRNA长期升高;在补液期间,这些升高的mRNA水平指导AVP生物合成的速率超过分泌需求;AVP mRNA积累似乎不受垂体或下丘脑AVP的直接调节。因此,要么必须假定AVP mRNA的半衰期异常长,大于或等于7天,要么即使在没有分泌刺激且细胞AVP储存完全补充后,仍必须持续刺激AVP基因转录。