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托瑞替酯对人肠上皮细胞中表皮生长因子诱导的DNA合成的增强作用。

Enhancement by tocoretinate of epidermal growth factor-induced DNA synthesis in human intestinal epithelial cells.

作者信息

Kawamura N, Miki K, Kurokawa K, Kojima I

机构信息

Cell Biology Research Unit, Institute of Endocrinology, Gunma University, Maebashi, Japan.

出版信息

Dig Dis Sci. 1994 Oct;39(10):2191-6. doi: 10.1007/BF02090370.

Abstract

Tocoretinate (TR) is a hybrid compound composed of alpha-tocopherol esterified with retinoic acid. The present study was conducted to clarify whether or not TR affects DNA synthesis in a human intestinal cell line, FHs 74 Int. In these cells, addition of 10% serum resulted in an approximately 10-fold increase in DNA synthesis as assessed by [3H]thymidine incorporation. Epidermal growth factor (EGF) augmented DNA synthesis three- to fourfold. When EGF was added together with insulin-like growth factor-I (IGF-I), which had only a small effect by itself, a combination of these growth factors reproduced the effect of serum. In quiescent FHs 74 Int cells, TR had no effect on DNA synthesis by itself. However, when quiescent cells were pretreated with TR for 24 hr, DNA synthesis induced by EGF was markedly enhanced. Thus, in TR-pretreated cells, EGF stimulated DNA synthesis to the same extent as 10% serum. The effect of TR was dose-dependent and the maximal effect was obtained by 10(-7) M TR. Pretreatment with TR enhanced the effect of EGF on DNA synthesis but did not change the dose-response relationship for EGF-mediated DNA synthesis. All-trans-retinoic acid had similar stimulatory effect on EGF-induced DNA synthesis. When the medium was changed during the treatment with TR, the effect of TR on DNA synthesis was reduced. In addition, pretreatment with TR resulted in release of immunoreactive IGF-I into medium. Finally, the effect of TR was attenuated by an addition of antibody against IGF-I.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

生育酚视黄酸酯(TR)是一种由视黄酸酯化的α-生育酚组成的杂合化合物。本研究旨在阐明TR是否会影响人肠道细胞系FHs 74 Int中的DNA合成。在这些细胞中,添加10%血清导致通过[3H]胸苷掺入评估的DNA合成增加约10倍。表皮生长因子(EGF)使DNA合成增加三到四倍。当EGF与胰岛素样生长因子-I(IGF-I)一起添加时(IGF-I本身作用较小),这些生长因子的组合重现了血清的作用。在静止的FHs 74 Int细胞中,TR本身对DNA合成没有影响。然而,当静止细胞用TR预处理24小时后,EGF诱导的DNA合成明显增强。因此,在TR预处理的细胞中,EGF刺激DNA合成的程度与10%血清相同。TR的作用是剂量依赖性的,10(-7) M的TR可获得最大效应。用TR预处理增强了EGF对DNA合成的作用,但没有改变EGF介导的DNA合成的剂量反应关系。全反式视黄酸对EGF诱导的DNA合成有类似的刺激作用。在用TR处理期间更换培养基时,TR对DNA合成的作用降低。此外,用TR预处理导致免疫反应性IGF-I释放到培养基中。最后,添加抗IGF-I抗体可减弱TR的作用。(摘要截断于250字)

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