Campantico E, Guastalla A
Dipartimento di Biologia animale dell'Università di Torino, Turin, Italy.
Gen Comp Endocrinol. 1992 May;86(2):197-202. doi: 10.1016/0016-6480(92)90102-p.
Single indirect immunocytochemical methods (immunofluorescence, PAP, and ABC) and double sequential staining (ABC followed by immunofluorescence) were used to localize GH- and PRL-producing cells in the pituitary distal lobe from Triturus cristatus. The following antisera were employed: rabbit anti-ovine PRL, anti-Rana catesbeiana PRL, anti-ovine GH, anti-bovine GH, and monkey anti-rat GH. A cell population corresponding to type-2 acidophils localized in the dorsal and central region, under the intermediate lobe, immunoreacted with GH antisera. Both ovine and bullfrog PRL antisera labeled a large cell population, corresponding to type-1 acidophils, predominantly localized in the ventral anterior two-thirds of the gland. The pattern of localization shown by the two cell types, although consistent with the majority of data on adult amphibians, disproves the findings obtained on the same species by other authors.
采用单间接免疫细胞化学方法(免疫荧光法、PAP法和ABC法)以及双重顺序染色法(ABC法后接免疫荧光法),对有冠蝾螈垂体远侧叶中产生生长激素(GH)和催乳素(PRL)的细胞进行定位。使用了以下抗血清:兔抗羊PRL、抗牛蛙PRL、抗羊GH、抗牛GH以及猴抗大鼠GH。位于中间叶下方背侧和中央区域的一群对应于2型嗜酸性细胞的细胞,与GH抗血清发生免疫反应。羊和牛蛙的PRL抗血清均标记了一群大细胞,对应于1型嗜酸性细胞,主要位于腺体腹侧前三分之二处。这两种细胞类型的定位模式虽然与大多数关于成年两栖动物的数据一致,但却与其他作者在同一物种上获得的研究结果相矛盾。