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大鼠垂体前叶中糖蛋白激素的免疫细胞化学定位。使用抗大鼠β亚基抗血清的光镜和电镜研究:包埋前和包埋后方法的比较。

Immunocytochemical localization of glycoprotein hormones in the rat anterior pituitary. A light and electron microscope study using antisera against rat bet subunits: a comparison between preembedding and postembeeding methods.

作者信息

Tougard C, Picart R, Tixier-Vidal A

出版信息

J Histochem Cytochem. 1980 Feb;28(2):101-14. doi: 10.1177/28.2.6986430.

Abstract

The binding sites of antisera (anti) to the beta (beta) subunits of rat follicle-stimulating hormone (rFSH), rat luteinizing hormone (rLH), and rat thyroid-stimulating hormone (rTSH) have been localized in rat anterior pituitaries by immunocytochemistry using light and electron microscopy. With the light microscope, LHbeta and FSHbeta were found in the same cells, which were violet after the alcian blue-periodic acid Schiff (AB-PAS) staining. TSHbeta was found in polygonal or stellate cells that were blue after AB-PAS. With the electron microscope, the thyrotropic cells contained very small secretory granules. LHbeta and FSHbeta were found in various types of cells (types A and B and their intermediate forms), which had previously been identified as gonadotropic cells. On serial ultrathin sections using the postembedding method the same cells and even some granules inside these cells were stained by both anti-rLHbeta and anti-rFSHbeta. A comparison of binding sites of anti-rLHbeta was performed using the preembeeding and the postembeeding methods. Antigenicity was observed on secretory granules whatever the method used. However, binding sites of anti-rLHbeta were detected inside the cisternae of the rough endoplasmic reticulum only with the preembedding method.

摘要

利用光学显微镜和电子显微镜,通过免疫细胞化学方法,已将抗大鼠促卵泡激素(rFSH)、大鼠促黄体生成素(rLH)和大鼠促甲状腺激素(rTSH)β亚基的抗血清(anti)结合位点定位在大鼠垂体前叶。在光学显微镜下,LHβ和FSHβ存在于同一细胞中,这些细胞在阿尔辛蓝-过碘酸希夫(AB-PAS)染色后呈紫色。TSHβ存在于AB-PAS染色后呈蓝色的多边形或星状细胞中。在电子显微镜下,促甲状腺细胞含有非常小的分泌颗粒。LHβ和FSHβ存在于各种类型的细胞(A 型和 B 型及其中间形式)中,这些细胞先前已被鉴定为促性腺细胞。使用包埋后方法对连续超薄切片进行观察,发现抗rLHβ和抗rFSHβ可对同一细胞甚至这些细胞内的一些颗粒进行染色。使用包埋前和包埋后方法对抗rLHβ的结合位点进行了比较。无论使用何种方法,在分泌颗粒上均观察到抗原性。然而,仅用包埋前方法在粗面内质网池内检测到抗rLHβ的结合位点。

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