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含多聚腺苷酸信使核糖核酸体外翻译后正常大鼠肝脏、再生大鼠肝脏及诺维科夫腹水肝癌细胞的核仁抗原特性

Characterization of nucleolar antigens of normal rat liver, regenerating rat liver, and Novikoff ascites hepatoma cells following in vitro translation of polyadenylic acid-containing messenger RNA.

作者信息

Satoh K, Busch H

出版信息

Cancer Res. 1983 May;43(5):2143-9.

PMID:6831440
Abstract

Nucleolar antigens of normal rat liver, regenerating liver, and Novikoff ascites hepatoma cells were transplanted in vitro from polyadenylic acid-containing messenger RNAs isolated from the respective tissues and immunoprecipitated with specific antinucleolar antibodies and Protein A. By two-dimensional gel electrophoresis of the translation products, five antigens were detected in normal rat liver. The antigens detected in 18-hr regenerating rat liver were the same as those of normal rat liver when immunoprecipitated with the anti-liver nucleolar antibodies. In the Novikoff tumor, 11 antigens were detected with anti-Novikoff nucleolar antibodies. Of these, two were not found in either normal or regenerating liver. Four major antigens were detectable in both Novikoff hepatoma and regenerating liver messenger RNA translation products with anti-Novikoff nucleolar antibodies. Two antigens were found in normal and regenerating liver that were not found in Novikoff hepatoma. In agreement with previous results, these immunoprecipitation analyses provide further evidence that some nucleolar antigens are present in Novikoff hepatoma that are not found in either normal or regenerating rat liver.

摘要

从正常大鼠肝脏、再生肝脏以及诺维科夫腹水肝癌细胞中提取含多聚腺苷酸的信使核糖核酸,在体外进行移植,并用特异性抗核仁抗体和蛋白A进行免疫沉淀,从而分析其核仁抗原。通过对翻译产物进行二维凝胶电泳,在正常大鼠肝脏中检测到了五种抗原。当用抗肝脏核仁抗体进行免疫沉淀时,在18小时再生大鼠肝脏中检测到的抗原与正常大鼠肝脏中的相同。在诺维科夫肿瘤中,用抗诺维科夫核仁抗体检测到了11种抗原。其中,有两种在正常肝脏或再生肝脏中均未发现。用抗诺维科夫核仁抗体在诺维科夫肝癌和再生肝脏信使核糖核酸翻译产物中均可检测到四种主要抗原。在正常肝脏和再生肝脏中发现了两种在诺维科夫肝癌中未发现的抗原。与之前的结果一致,这些免疫沉淀分析进一步证明,诺维科夫肝癌中存在一些在正常大鼠肝脏或再生大鼠肝脏中均未发现的核仁抗原。

相似文献

1
Characterization of nucleolar antigens of normal rat liver, regenerating rat liver, and Novikoff ascites hepatoma cells following in vitro translation of polyadenylic acid-containing messenger RNA.含多聚腺苷酸信使核糖核酸体外翻译后正常大鼠肝脏、再生大鼠肝脏及诺维科夫腹水肝癌细胞的核仁抗原特性
Cancer Res. 1983 May;43(5):2143-9.
2
Differences in nucleolar antigens of rat liver and Novikoff hepatoma ascites cells.大鼠肝脏和诺维科夫肝癌腹水细胞的核仁抗原差异。
Cancer Res. 1978 Jul;38(7):1906-15.
3
Nucleolar phosphoproteins of normal rat liver and Novikoff hepatoma ascites cells.正常大鼠肝脏和诺维科夫肝癌腹水细胞的核仁磷蛋白。
Cancer Res. 1975 Jun;35(6):1470-5.
4
Purification and partial characterization of nucleolar antigen-1 of the Novikoff hepatoma.诺维科夫肝癌核仁抗原-1的纯化及部分特性分析
Cancer Res. 1979 Jan;39(1):59-66.
5
Antigenically active nonhistone chromatin proteins in cancer cells.癌细胞中具有抗原活性的非组蛋白染色质蛋白。
Cancer Res. 1976 Sep;36(9 PT 2):3399-408.
6
Adsorption of messenger RNA of Novikoff hepatoma, normal liver, and regenerating liver on complementary DNA-cellulose affinity matrices.诺维科夫肝癌、正常肝脏和再生肝脏的信使核糖核酸在互补脱氧核糖核酸-纤维素亲和基质上的吸附作用
Cancer Res. 1977 Oct;37(10):3694-700.
7
Identification of polysomes synthesizing Novikoff hepatoma nucleolar antigens.合成诺维科夫肝癌核仁抗原的多核糖体的鉴定。
Cancer Res. 1980 May;40(5):1367-71.
8
Two-dimensional gel electrophoresis of nuclear phosphoproteins of Novikoff hepatoma and regenerating liver.诺维科夫肝癌和再生肝细胞核磷蛋白的二维凝胶电泳
Physiol Chem Phys. 1980;12(1):11-20.
9
Purification and characterization of cytosol protein 45/7.8 present in rapidly growing hepatomas.快速生长型肝癌中存在的胞质溶胶蛋白45/7.8的纯化与特性分析
Cancer Res. 1980 May;40(5):1623-9.
10
Two-dimensional gel electrophoretic comparison of proteins of nuclear fractions of normal liver and Novikoff hepatoma.
Cancer Res. 1979 Feb;39(2 Pt 1):507-18.

引用本文的文献

1
Association between the mammalian 110,000-dalton heat-shock protein and nucleoli.哺乳动物110,000道尔顿热休克蛋白与核仁之间的关联。
J Cell Biol. 1983 Nov;97(5 Pt 1):1389-95. doi: 10.1083/jcb.97.5.1389.
2
Purification, induction, and distribution of placental glutathione transferase: a new marker enzyme for preneoplastic cells in the rat chemical hepatocarcinogenesis.胎盘谷胱甘肽转移酶的纯化、诱导及分布:大鼠化学性肝癌发生过程中一种新的癌前细胞标志物酶
Proc Natl Acad Sci U S A. 1985 Jun;82(12):3964-8. doi: 10.1073/pnas.82.12.3964.