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甲胎蛋白在正常及病变肝脏中的免疫组织学定位

Immunohistological localization of alpha 1-fetoprotein in normal and diseased liver.

作者信息

Kuhlmann W D, Kuhlmann M

出版信息

Acta Histochem Suppl. 1982;25:63-8.

PMID:6178134
Abstract

Cellular alpha 1-fetoprotein (AFP) is localized by light and electron microscopic immunoperoxidase methods. For light microscopic studies we employed ethanol-acetic acid fixed and paraffin embedded liver blocks. For the ultrastructural localization of AFP, formaldehyde-glutaraldehyde fixed tissues were used in preembedding phase. The occurrence of AFP was studied in normal and diseased livers of mice and rats: (a) fetal and neonatal livers; (b) liver regeneration after CCl4 intoxication; (c) chemical hepatocarcinogenesis. During ontogenesis, AFP is detected in perinuclear spaces, in lamellae of the RER and in the Golgi apparatus of fetal and postnatal hepatocytes. After CCl4 intoxication of low and high AFP producing mouse strains, cellular AFP is found in hepatocytes of portal, periportal and intermediate zones. Hepatocytes in front of the necroses usually contain the strongest reactions. In early stage of hepatocarcinogenesis, AFP is localized in proliferating oval-shaped cells when injured livers regenerate. At the stage of malignant conversion, distinct AFP staining and non-AFP staining hepatocellular carcinomas occur.

摘要

通过光学显微镜和电子显微镜免疫过氧化物酶方法对细胞α1-甲胎蛋白(AFP)进行定位。对于光学显微镜研究,我们使用乙醇-乙酸固定并石蜡包埋的肝组织块。为了对AFP进行超微结构定位,在包埋前阶段使用甲醛-戊二醛固定的组织。在小鼠和大鼠的正常及患病肝脏中研究AFP的存在情况:(a)胎儿和新生儿肝脏;(b)四氯化碳中毒后的肝脏再生;(c)化学性肝癌发生。在个体发育过程中,在胎儿和出生后肝细胞的核周间隙、粗面内质网片层和高尔基体中检测到AFP。对产生低水平和高水平AFP的小鼠品系进行四氯化碳中毒后,在门周、门周周围和中间区的肝细胞中发现细胞AFP。坏死灶前方的肝细胞通常反应最强。在肝癌发生的早期阶段,当受损肝脏再生时,AFP定位于增殖的椭圆形细胞中。在恶性转化阶段,出现明显的AFP染色和非AFP染色的肝细胞癌。

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