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v-src基因表达对胚胎癌细胞分化的影响。

The effects of v-src expression on the differentiation of embryonal carcinoma cells.

作者信息

Boulter C A, Wagner E F

机构信息

European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.

出版信息

Oncogene. 1988 Mar;2(3):207-14.

PMID:3127777
Abstract

We have used replication-defective selectable retroviruses to express inducibly or constitutively the v-src gene in the embryonal carcinoma (EC) cell lines F9, PC13 and P19. High v-src expression in F9 and PC13 cells does not induce or disrupt their differentiation. In contrast, P19 cells expressing high levels of v-src have a 'differentiated' morphology and are unable to respond to signals that normally induce differentiation along the neural or muscle pathways. Regulation of v-src transcription from the inducible human metallothionein (MT) promoter has shown that v-src expression above a threshold level induces differentiation of these cells, as defined by loss of the stem cell marker ECMA-7. These results suggest that v-src expression may be compatible with differentiation events occurring early in embryogenesis, represented by F9 and PC13 cell differentiation, but might disrupt the differentiation of cell types present at later developmental stages.

摘要

我们已使用复制缺陷型可选择逆转录病毒在胚胎癌细胞系F9、PC13和P19中诱导性或组成性表达v-src基因。F9和PC13细胞中v-src的高表达不会诱导或破坏它们的分化。相反,表达高水平v-src的P19细胞具有“分化”形态,并且无法对通常诱导沿神经或肌肉途径分化的信号作出反应。来自可诱导的人金属硫蛋白(MT)启动子的v-src转录调控表明,高于阈值水平的v-src表达会诱导这些细胞分化,这是由干细胞标志物ECMA-7的丧失所定义的。这些结果表明,v-src表达可能与胚胎发育早期发生的分化事件兼容,如F9和PC13细胞分化所代表的,但可能会破坏后期发育阶段存在的细胞类型的分化。

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