Lombardero Matilde, Quintanar-Stephano Andres, Vidal Sergio, Horvath Eva, Kovacs Kalman, Lloyd Ricardo V, Scheithauer Bernd W
Department of Anatomy and Animal Production, University of Santiago de Compostela, Lugo, Spain.
J Anat. 2009 Feb;214(2):235-44. doi: 10.1111/j.1469-7580.2008.01037.x.
Estrogens are known to cause pituitary enlargement and lactotroph proliferation. They also modulate pituitary angiogenesis and induce tumor formation. Pituitary grafts, due to the loss of hypothalamic dopamine, also show lactotroph hyperplasia. We investigated the role of estrogen on rat pituitary autograft vascularization by light and transmission electron microscopy, and assessed prolactin (PRL) blood levels, microvessel density (MVD) and cell proliferation using the BrdU labeling index. All adenohypophysial cell types were identified by immunohistochemistry (streptavidin-biotin-peroxidase complex method). The proangiogenic factors, vascular endothelial growth factor (VEGF), its receptor Flk-1, and hypoxia inducible factor-1alpha (HIF-1alpha) were similarly demonstrated. The prevalence of lactotrophs, as well as more intense staining for VEGF, Flk-1 and HIF-1alpha, was noted in those grafts exposed to estrogen, mainly in the area surrounding the central necrotic core. Immunostaining showed Flk-1 expression increased in endothelial cells of the estrogen-exposed grafts as compared with those unexposed. In contrast to the grafts not exposed to estrogen, in the estrogen-exposed grafts, only fenestrated endothelium could be demonstrated, suggesting that estrogen induces fenestration of newly formed capillaries. There was an increase in blood PRL levels in the estrogen-treated groups as compared with controls. Both MVD and BrdU labeling indices were higher in grafts exposed to estrogen, especially after 4 weeks. Our results suggest that estrogen administration not only enhances the expression of proangiogenic factors in the pituitary grafts but also induces their expression at earlier stages, leading to rapid neoformation of purely fenestrated capillaries.
已知雌激素会导致垂体增大和催乳细胞增殖。它们还能调节垂体血管生成并诱导肿瘤形成。由于下丘脑多巴胺缺失,垂体移植也会出现催乳细胞增生。我们通过光学显微镜和透射电子显微镜研究了雌激素对大鼠垂体自体移植血管化的作用,并使用BrdU标记指数评估催乳素(PRL)血水平、微血管密度(MVD)和细胞增殖。通过免疫组织化学(链霉亲和素-生物素-过氧化物酶复合物法)鉴定所有腺垂体细胞类型。同样证实了促血管生成因子血管内皮生长因子(VEGF)、其受体Flk-1和缺氧诱导因子-1α(HIF-1α)的存在。在暴露于雌激素的那些移植中,尤其是在中央坏死核心周围区域,观察到催乳细胞的比例增加,以及VEGF、Flk-1和HIF-1α的染色更强。免疫染色显示,与未暴露于雌激素的移植相比,暴露于雌激素的移植中内皮细胞中Flk-1表达增加。与未暴露于雌激素的移植相反,在暴露于雌激素的移植中,仅能证实有窗孔内皮,这表明雌激素诱导新形成的毛细血管形成窗孔。与对照组相比,雌激素处理组的血PRL水平升高。暴露于雌激素的移植中MVD和BrdU标记指数均较高,尤其是在4周后。我们的结果表明,给予雌激素不仅能增强垂体移植中促血管生成因子的表达,还能在更早阶段诱导其表达,导致快速形成纯窗孔毛细血管的新生血管。