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猿猴病毒40诱导的仓鼠肿瘤细胞系的正常变体和回复转化变体中的神经节苷脂模式及表型特征

Ganglioside patterns and phenotypic characteristics in a normal variant and a transformed back variant of a simian virus 40-induced hamster tumor cell line.

作者信息

Nigam V N, Lallier R, Brailovsky C

出版信息

J Cell Biol. 1973 Aug;58(2):307-16. doi: 10.1083/jcb.58.2.307.

Abstract

Ganglioside patterns of a cloned Simian virus 40- (SV40) induced hamster tumor cell (Cl(2)TSV(5)-S), its normal variant (Cl(2)TSV(5)-R) which are Cl(2)TSV(5)-S gradually adapted to grow in the presence of 2 microg/ml actinomycin D and exhibit certain normal phenotypic characteristics, and its back variant (Cl(2)TSV(5)-RR), which are Cl(2)TSV(5)-R cells grown in the absence of actinomycin D for more than 60 passages and which exhibit greater phenotypic similarity to Cl(2)TSV(5)-S cells, have been analyzed. All three cell lines contain N(acetylneuraminyl) galactosylglycosyl ceramide (hematoside, GM(3)), N-acetylgalactosaminyl (N-acetylneuraminyl) galactosylglucosyl ceramide (GM(2)), and a higher ganglioside tentatively identified as disialohematoside. However, Cl(2)TSV(5)-R have more GM(2) than Cl(2)TSV(5)-S whereas Cl(2)TSV(5)-RR contain an intermediate amount of GM(2). The amount of GM(2) is correlative with the activity of UDP-N-acetylgalactosamine: hematoside N-acetylgalactosaminyl transferase in the extract of the three cell lines and with their agglutination by wheat germ agglutinin.

摘要

已对一种克隆的猿猴病毒40(SV40)诱导的仓鼠肿瘤细胞(Cl(2)TSV(5)-S)、其正常变体(Cl(2)TSV(5)-R)以及其回复变体(Cl(2)TSV(5)-RR)的神经节苷脂模式进行了分析。Cl(2)TSV(5)-R是Cl(2)TSV(5)-S在2微克/毫升放线菌素D存在下逐渐适应生长并表现出某些正常表型特征的变体,而Cl(2)TSV(5)-RR是在无放线菌素D的情况下培养超过60代的Cl(2)TSV(5)-R细胞,其与Cl(2)TSV(5)-S细胞表现出更大的表型相似性。所有这三种细胞系都含有N-(乙酰神经氨酰基)半乳糖基糖基神经酰胺(血苷脂,GM(3))、N-乙酰半乳糖胺基(N-乙酰神经氨酰基)半乳糖基葡糖基神经酰胺(GM(2))以及一种暂定为双唾液酸血苷脂的高级神经节苷脂。然而,Cl(2)TSV(5)-R中的GM(2)比Cl(2)TSV(5)-S中的多,而Cl(2)TSV(5)-RR中的GM(2)含量处于中间水平。GM(2)的量与这三种细胞系提取物中UDP-N-乙酰半乳糖胺:血苷脂N-乙酰半乳糖胺基转移酶的活性以及它们被麦胚凝集素凝集的情况相关。

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本文引用的文献

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Ganglioside patterns of three morris minimal deviation hepatomas.
FEBS Lett. 1970 Dec;11(3):181-184. doi: 10.1016/0014-5793(70)80523-3.

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