Suppr超能文献

腐胺不支持IEC-6细胞的迁移和生长。

Putrescine does not support the migration and growth of IEC-6 cells.

作者信息

Yuan Q, Viar M J, Ray R M, Johnson L R

机构信息

Department of Physiology, College of Medicine, University of Tennessee, Memphis, Tennessee 38163, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2000 Jan;278(1):G49-56. doi: 10.1152/ajpgi.2000.278.1.G49.

Abstract

The migration of IEC-6 cells is inhibited when the cells are depleted of polyamines by inhibiting ornithine decarboxylase with alpha-difluoromethylornithine (DFMO). Exogenous putrescine, spermidine, and spermine completely restore cell migration inhibited by DFMO. Because polyamines are interconverted during their synthesis and catabolism, the specific role of individual polyamines in intestinal cell migration, as well as growth, remains unclear. In this study, we used an inhibitor of S-adenosylmethionine decarboxylase, diethylglyoxal bis(guanylhydrazone)(DEGBG), to block the synthesis of spermidine and spermine from putrescine. We found that exogenous putrescine does not restore migration and growth of IEC-6 cells treated with DFMO plus DEGBG, whereas exogenous spermine does. In addition, the normal distribution of actin filaments required for migration, which is disrupted in polyamine-deficient cells, could be achieved by adding spermine but not putrescine along with DFMO and DEGBG. These results indicate that putrescine, by itself, is not essential for migration and growth, but that it is effective because it is converted into spermidine and/or spermine.

摘要

当用α-二氟甲基鸟氨酸(DFMO)抑制鸟氨酸脱羧酶使IEC-6细胞中的多胺耗尽时,IEC-6细胞的迁移受到抑制。外源性腐胺、亚精胺和精胺可完全恢复被DFMO抑制的细胞迁移。由于多胺在其合成和分解代谢过程中会相互转化,因此单个多胺在肠道细胞迁移以及生长中的具体作用仍不清楚。在本研究中,我们使用S-腺苷甲硫氨酸脱羧酶抑制剂二乙二醛双(脒腙)(DEGBG)来阻断从腐胺合成亚精胺和精胺。我们发现,外源性腐胺不能恢复用DFMO加DEGBG处理的IEC-6细胞的迁移和生长,而外源性精胺可以。此外,迁移所需的肌动蛋白丝的正常分布在多胺缺乏的细胞中会被破坏,通过与DFMO和DEGBG一起添加精胺而非腐胺可以实现这种正常分布。这些结果表明,腐胺本身对于迁移和生长并非必不可少,但它之所以有效是因为它会转化为亚精胺和/或精胺。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验