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导入胚胎癌细胞的诱导型c-fos基因的促分化潜能分析。

Analysis of the differentiation-promoting potential of inducible c-fos genes introduced into embryonal carcinoma cells.

作者信息

Rüther U, Wagner E F, Müller R

出版信息

EMBO J. 1985 Jul;4(7):1775-81. doi: 10.1002/j.1460-2075.1985.tb03850.x.

Abstract

To investigate the differentiation-promoting potential of c-fos in embryonal carcinoma cells (EC cells) we have designed various human metallothionein promoter-mouse-c-fos gene constructs containing also the selectable SV40 promoter-driven neo gene. Upon transfection into F9 EC cells and selection for neo resistance, the following results were obtained. (i) With each of the constructs, colonies of morphologically altered and differentiated (i.e., TROMA-1 and TROMA-3 expressing) cells were identified. (ii) Expression of c-fos was required to affect the differentiation state of F9 cells to a significant extent, but a low level was sufficient; no enhancement of differentiation was noticeable even after 100-fold induction of c-fos expression by cadmium. (iii) F9 cell clones were isolated which, in spite of very high levels of exogenous c-fos expression, had stem cell morphology. These cells, however, continuously generated morphologically altered and differentiated cells upon subculturing. (iv) In other EC cell lines, which resemble stem cells more closely than the 'partially differentiated' F9 cells, c-fos expression showed either a less pronounced (P19 cells) or no differentiation-promoting effect at all (PC13 cells). Our results suggest that the c-fos gene product acts in concert with other, probably 'spontaneously' occurring events to promote differentiation of certain EC cell lines.

摘要

为了研究原癌基因c-fos在胚胎癌细胞(EC细胞)中的促分化潜能,我们设计了多种含有人金属硫蛋白启动子的小鼠c-fos基因构建体,这些构建体还包含可选择的SV40启动子驱动的新霉素抗性基因(neo基因)。将这些构建体转染到F9 EC细胞中并筛选新霉素抗性后,得到了以下结果。(i)对于每个构建体,均鉴定出形态改变且分化的(即表达TROMA-1和TROMA-3的)细胞集落。(ii)c-fos的表达对于显著影响F9细胞的分化状态是必需的,但低水平即可;即使在用镉诱导c-fos表达增加100倍后,也未观察到分化增强。(iii)分离出了F9细胞克隆,尽管外源c-fos表达水平很高,但这些细胞具有干细胞形态。然而,这些细胞在传代培养时会持续产生形态改变且分化的细胞。(iv)在其他比“部分分化的”F9细胞更类似于干细胞的EC细胞系中,c-fos表达要么显示出不太明显的促分化作用(P19细胞),要么根本没有促分化作用(PC13细胞)。我们的结果表明,c-fos基因产物与其他可能“自发”发生的事件协同作用,以促进某些EC细胞系的分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03e7/554417/597ab8b7710b/emboj00272-0155-a.jpg

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