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鸟氨酸脱羧酶抑制对小鼠红白血病细胞增殖和分化过程中c-myc表达的影响。

Effects of ornithine decarboxylase inhibition on c-myc expression during murine erythroleukemia cell proliferation and differentiation.

作者信息

Watanabe T, Sherman M, Shafman T, Iwata T, Kufe D

出版信息

J Cell Physiol. 1986 Jun;127(3):480-4. doi: 10.1002/jcp.1041270319.

Abstract

The polyamines putrescine, spermidine, and spermine have been implicated in the regulation of cellular proliferation and differentiation. We have previously demonstrated that spermidine is required for proliferation of murine Friend erythroleukemia (MEL) cells. We have also shown that spermidine is required at a transcriptional level for induction of MEL globin synthesis. Since studies monitoring c-myc expression have suggested that this gene also plays a role in both growth and differentiation, we have monitored the effects of inhibiting ornithine decarboxylase (ODCase) activity and polyamine synthesis on levels of c-myc transcripts. The results demonstrate that the level of c-myc RNA is independent of ODCase inhibition and depletion of intracellular spermidine. More importantly, arrest of MEL proliferation is not associated with detectable changes in c-myc expression, while under these conditions there is a decline in ODCase transcripts. During induction of MEL differentiation with dimethyl sulfoxide (DMSO) and hexamethylene bisacetamide (HMBA), c-myc and ODCase undergo similar changes in patterns of expression. However, although spermidine is required for appearance of the differentiated MEL phenotype, depletion of this polyamine by ODCase inhibition had no detectable effect on the biphasic changes in c-myc RNA observed during MEL differentiation. Thus, these biphasic changes in c-myc expression are not sufficient for induction of the mature phenotype. Finally, these results would indicate that the regulation of c-myc expression during both proliferation and differentiation is independent of ODCase activity and inhibition of proliferation by spermidine depletion.

摘要

多胺腐胺、亚精胺和精胺与细胞增殖和分化的调节有关。我们之前已经证明,亚精胺是小鼠Friend红白血病(MEL)细胞增殖所必需的。我们还表明,在转录水平上,亚精胺是诱导MEL珠蛋白合成所必需的。由于监测c-myc表达的研究表明该基因在生长和分化中也起作用,我们监测了抑制鸟氨酸脱羧酶(ODCase)活性和多胺合成对c-myc转录本水平的影响。结果表明,c-myc RNA的水平与ODCase抑制和细胞内亚精胺的消耗无关。更重要的是,MEL增殖的停滞与c-myc表达的可检测变化无关,而在这些条件下ODCase转录本会下降。在用二甲基亚砜(DMSO)和六亚甲基双乙酰胺(HMBA)诱导MEL分化的过程中,c-myc和ODCase的表达模式发生了类似的变化。然而,尽管亚精胺是分化的MEL表型出现所必需的,但通过抑制ODCase来消耗这种多胺对MEL分化过程中观察到的c-myc RNA的双相变化没有可检测到的影响。因此,c-myc表达的这些双相变化不足以诱导成熟表型。最后,这些结果表明,在增殖和分化过程中c-myc表达的调节与ODCase活性以及通过消耗亚精胺来抑制增殖无关。

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