[前列腺和前列腺癌的免疫组织化学]。

N Wernert
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引用次数: 0

摘要

1. 从胎儿时期到青春期,前列腺和导管的未成熟多层上皮对以下抗原反应积极:酸性前列腺磷酸酶(PAP)、前列腺特异性抗原(PSA)、角蛋白抗体广泛反应的角蛋白“AE1 + AE3”、角质层角蛋白、角蛋白7、8、18和19、花生凝集素(PNA)和癌胚抗原(CEA)的结合位点。PAP和PSA的表达各不相同,个别病例甚至不存在。α -1抗凝乳胰蛋白酶(ACT)直到出生时才被证实。它仅在三分之二的病例中被发现是局部的。前列腺基质对静脉溶酶和desmin均呈阳性。在前列腺中,波形蛋白可局部发生。胎儿前列腺鳞状细胞化生的所有抗角蛋白抗血清以及PNA和CEA均呈阳性。射精管和精囊上皮的所有角蛋白均呈阳性。在一般的基础上发现了蛋白蛋白和rna结合位点。前列腺尿道的尿路上皮也含有所有角蛋白,此外还有PNA和CEA。5 -羟色胺阳性的内分泌细胞在前列腺、前列腺导管和尿路上皮中稀少。2. 青春期雄激素作用的发生很可能导致未成熟腺上皮在形态上分化为基底细胞和分泌柱状上皮两种细胞类型,这两种细胞类型在免疫组织化学行为上有所不同。良性结节增生的腺体,包括特殊形式,以及核异型性上皮改变的免疫组织化学行为与正常前列腺完全相同。标记物PAP、PSA、CEA、ACT、角蛋白8和18以及局灶性波形蛋白仅在前列腺和导管的分泌上皮中表达,而不在基底细胞中表达。相比之下,针对以下抗原的抗血清仅染色基底细胞和基底细胞增生:角质层角蛋白,角蛋白4、5和6的共同表位(抗体KA1)以及雌激素和孕激素受体。鳞状细胞化生的免疫组织化学行为与基底细胞相似。在基底细胞和分泌上皮中均发现角蛋白7和19、desmoplakin、PNA以及患者自身的血型抗原。角蛋白7和血型抗原总是只在局部发现。pna结合位点由圆筒状上皮分泌。萎缩腺体和营养增生后的腺体与基底细胞和分泌上皮具有相同的免疫组织化学特征。(摘要删节为400字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Immunohistochemistry of the prostate and prostate carcinomas].

1. The immature multilayered epithelium of the prostate glands and ducts reacts positively throughout the fetal period up to puberty for the following antigens: Acid prostate phosphatase (PAP), the prostate-specific antigen (PSA), keratins demonstrated by the broadly reacting keratin antibody "AE1 + AE3", keratins from stratum corneum, the keratins 7, 8, 18 and 19, binding sites for the peanut agglutinin (PNA) and carcinoembryonic antigen (CEA). The expression of PAP and PSA varies and can in individual cases even be nonexistent. Alpha-1-antichymotrypsin (ACT) is not demonstrable until birth. It is found only focally in two thirds of the cases. The prostate stroma proves positive for vimentin as well as desmin. In the prostate glands, vimentin may occur focally. Squamous cell metaplasias in the fetal prostate show positive for all antikeratin antisera as well as PNA and CEA. The epithelium of the ejaculatory ducts and seminal vesicles proves positive for all keratins investigated. Vimentin as well as PNA-binding sites are found on a general basis. The urothelium of the prostate urethra also contains all keratins and, in addition, PNA and CEA. Endocrine cells, positive for serotonin, are sparse in the prostate glands, in the prostatic ducts and in the urothelium. 2. The onset of the androgen effect during puberty leads very probably to the morphological differentiation of the immature glandular epithelium into the two cell types, basal cell and secretory cylindric epithelium which differ with regard to their immunohistochemical behavior. The glands of benign nodular hyperplasia, including special forms, as well as epithelial alterations with nuclear atypia behave immunohistochemically exactly like normal prostate glands. The markers PAP, PSA, CEA, ACT, the keratins 8 and 18 and focally occurring vimentin are expressed exclusively in the secretory epithelium of the prostate glands and ducts, and not in the basal cells. In contrast, antisera against the following antigens stain only the basal cells and basal cell hyperplasia: Keratins from stratum corneum, a common epitope of the keratins 4, 5 and 6 (antibody KA1) and both the estrogen and progesterone receptor. Squamous cell metaplasias behave immunohistochemically like the basal cells. The keratins 7 and 19, desmoplakin, PNA as well as the patients' own blood group antigens are found in both the basal cells and the secretory epithelium. Keratin 7 and the blood group antigens are always only found focally. PNA-binding sites are secreted by the cylindric epithelium. Atrophic glands and the glands in postatrophic hyperplasia share immunohistochemical features with both the basal cells and the secretory epithelium.(ABSTRACT TRUNCATED AT 400 WORDS)

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