f1881结合蛋白在人良性前列腺肥大组织中的组织化学观察。

Investigative urology Pub Date : 1981-03-01
H Naito, H Ito, M Wakisaka, A Kambegawa, J Shimazaki
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引用次数: 0

摘要

将r1881的3-羧基甲基肟偶联物与牛血清白蛋白偶联,并与异硫氰酸荧光素反应。用该化合物孵育良性前列腺肥大患者的组织切片。在腺体细胞的细胞质中可见荧光,虽然阳性细胞和阴性细胞在某些区域均匀分布。上皮细胞间质和细胞核均无荧光。用20倍摩尔过量的r1881 -羧甲基肟-牛血清白蛋白、1微米的r1881或1微米的曲安奈德进行预孵育,可使切片的荧光减弱。牛血清白蛋白结合异硫氰酸荧光素未染色切片。因此,在切片中观察到的荧光似乎归因于r1881的高亲和力结合。荧光细胞的强度和数量与生化方法估计的r1881结合具有良好的相关性。
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Histochemical observation of F 1881 binding protein in human benign prostatic hypertrophy.

A 3-carboxymethyloxime conjugate of R 1881 was conjugated with bovine serum albumin and reacted with fluorescein isothiocyanate. Tissue sections from patients with benign prostatic hypertrophy were incubated with this compound. Fluorescence was observed in the cytoplasm of gland cells, although both positive and negative cells were distributed evenly in some areas. Neither the stroma nor the nuclei of epithelial cells were fluorescent. Preincubation with a 20 fold molar excess of R 1881-carboxymethyloxime-bovine serum albumin, 1 microM of R 1881, or 1 microM of triamcinolone acetonide diminished fluorescence of the section. Bovine serum albumin conjugated with fluorescein isothiocyanate did not stain the section. Therefore, the fluorescence observed in the sections seems to be attributable to the high affinity binding of R 1881. The intensity and number of fluorescent cells and the R 1881 binding estimated by a biochemical method were well correlated.

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