Morel G, Besson J, Rosselin G, Dubois P M
Neuroendocrinology. 1982 Feb;34(2):85-9. doi: 10.1159/000123282.
The immunocytological method was used to investigate whether vasoactive intestinal peptide (VIP) is present in the pituitary gland and to localize the peptide at the cellular and subcellular levels. Pituitaries of Wistar male and female rats (Iffa Credo) were fixed in glutaraldehyde 2.5% and postosmicated and frozen in liquid nitrogen. Ultrathin slices, obtained by cryo-ultramicrotomy were incubated with the antiserum. The antigen-antibody reaction was detected by peroxidase-antiperoxidase complexes revealed by 4-chloro-1-naphtol. The prolactin (PRL)-secreting cells were identified by using an anti-oPRL antiserum. The PRL immunoreactivity was localized in secretory granules of irregular shapes. An anti-VIP serum was used which neither cross-reacted with the several fragments of VIP molecule nor with peptides from gut or hypothalamus. The VIP immunoreactivity obtained with this antiserum, was observed in PRL cells only but never in so-matotropic, gonadotropic, corticotropic and thyrotropic cells. The immunoreactivity was localized in the cytoplasmic matrix between and around the secretory granules but not in the organelles, and in the nucleus distributed all over the euchromatin near to the heterochromatin regions. No reaction was observed by using either nonimmune serum or anti-VIP antiserum incubated with VIP. No modification of VIP immunoreactivity was observed by using anti-VIP antiserum incubated with somatostatin, gonado- or thyroliberin. These data (1) provide immunocytological evidence for presence of VIP in pituitary gland; (2) indicate the presence of this peptide in one particular pituitary cell type, and (3) support the hypothesis that VIP could have a direct effect on the control of PRL secretion.
采用免疫细胞学法研究血管活性肠肽(VIP)是否存在于垂体中,并在细胞及亚细胞水平对该肽进行定位。选用了Iffa Credo公司的雄性和雌性Wistar大鼠垂体,将其固定于2.5%的戊二醛中,后经锇酸处理并在液氮中冷冻。通过冷冻超薄切片显微术获得的超薄切片与抗血清一起孵育。抗原 - 抗体反应通过4 - 氯 - 1 - 萘酚显示的过氧化物酶 - 抗过氧化物酶复合物进行检测。使用抗oPRL抗血清鉴定催乳素(PRL)分泌细胞。PRL免疫反应性定位于不规则形状的分泌颗粒中。使用的抗VIP血清既不与VIP分子的几个片段交叉反应,也不与来自肠道或下丘脑的肽交叉反应。用该抗血清获得的VIP免疫反应性仅在PRL细胞中观察到,而在生长激素细胞、促性腺激素细胞、促肾上腺皮质激素细胞和促甲状腺激素细胞中从未观察到。免疫反应性定位于分泌颗粒之间及周围的细胞质基质中,而非细胞器中,并且在细胞核中分布于靠近异染色质区域的整个常染色质中。使用非免疫血清或与VIP一起孵育的抗VIP抗血清均未观察到反应。用与生长抑素、促性腺激素释放激素或促甲状腺激素释放激素一起孵育的抗VIP抗血清未观察到VIP免疫反应性的改变。这些数据(1)为垂体中存在VIP提供了免疫细胞学证据;(2)表明该肽存在于一种特定的垂体细胞类型中;(3)支持VIP可能对PRL分泌控制有直接作用的假说。