Hyodo S, Yamada C, Takezawa T, Urano A
Department of Regulation Biology, Faculty of Sciences, Saitama University, Japan.
Neuroscience. 1992;46(1):241-50. doi: 10.1016/0306-4522(92)90024-v.
We investigated the ontogeny of provasopressin gene expression in neurosecretory neurons of the supraoptic and paraventricular nuclei of developing mice by semi-quantitative in situ hybridization and immunohistochemical techniques in combination with stereometry of vasopressin-immunoreactive neurons. Provasopressin mRNA was detected in paraffin sections using a mixture of radiolabeled synthetic oligonucleotide probes complementary to the mRNA loci encoding vasopressin (2-9) and vasopressin neurophysin (1-8). Vasopressin immunoreactivity was located with a polyclonal anti-vasopressin antiserum and a monoclonal anti-vasopressin-neurophysin antibody either with or without enhancing technique for the diaminobenzidine reaction. Autoradiographic hybridization signals that indicate the localization of provasopressin mRNA were first detected on embryonic day 15 in the supraoptic nucleus and embryonic day 18 in the paraventricular nucleus. Vasopressin immunoreactivity was first found in the median eminence on embryonic day 14, and then in the supraoptic and paraventricular nuclei on embryonic days 15 and 16, respectively. The provasopressin mRNA levels were markedly increased in both the supraoptic and the paraventricular nuclei just after birth. The immunoreactivity of vasopressin neurons was drastically decreased in both nuclei on postnatal days 1 and 2, suggesting marked vasopressin release in the neonates. Cross-sectional areas of vasopressin-immunoreactive somata and their cell nuclei gradually increased in both the supraoptic and the paraventricular nuclei during the perinatal period by day 5, and then attained adult size between days 10 and 20. During this phase, the level of provasopressin mRNA remained low compared with that in the adult magnocellular neurosecretory cells. These results indicate that the expression of provasopressin gene is markedly increased in both the supraoptic and the paraventricular nuclei soon after birth. Secretory activity of vasopressin neurons is elevated in neonatal mice. Vasopressin may have an important osmoregulatory role in neonatal mice undergoing drastic changes in water metabolism following birth.
我们通过半定量原位杂交和免疫组织化学技术,结合血管加压素免疫反应性神经元的立体测量法,研究了发育中小鼠视上核和室旁核神经分泌神经元中前血管加压素基因表达的个体发生。使用与编码血管加压素(2 - 9)和血管加压素神经垂体素(1 - 8)的mRNA位点互补的放射性标记合成寡核苷酸探针混合物,在石蜡切片中检测前血管加压素mRNA。使用多克隆抗血管加压素抗血清和单克隆抗血管加压素 - 神经垂体素抗体定位血管加压素免疫反应性,无论有无增强二氨基联苯胺反应的技术。指示前血管加压素mRNA定位的放射自显影杂交信号首先在胚胎第15天在视上核中检测到,在胚胎第18天在室旁核中检测到。血管加压素免疫反应性首先在胚胎第14天在正中隆起中发现,然后分别在胚胎第15天和第16天在视上核和室旁核中发现。出生后,视上核和室旁核中的前血管加压素mRNA水平均显著增加。出生后第1天和第2天,两个核中血管加压素神经元的免疫反应性急剧下降,表明新生儿中血管加压素大量释放。在围产期到第5天期间,视上核和室旁核中血管加压素免疫反应性胞体及其细胞核的横截面积逐渐增加,然后在第10天到第20天之间达到成年大小。在此阶段,与成年大细胞神经分泌细胞相比,前血管加压素mRNA水平仍然较低。这些结果表明,出生后不久,视上核和室旁核中前血管加压素基因的表达显著增加。新生小鼠中血管加压素神经元的分泌活性升高。血管加压素可能在出生后水代谢发生剧烈变化的新生小鼠中具有重要的渗透压调节作用。