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在暴露于脱氧胆酸盐的人结肠上皮细胞中,GADD基因表达增加。

Increased GADD gene expression in human colon epithelial cells exposed to deoxycholate.

作者信息

Scott David W, Mutamba Sophia, Hopkins Robin G, Loo George

机构信息

Cellular and Molecular Nutrition Research Laboratory, Graduate Program in Nutrition, University of North Carolina at Greensboro, Greensboro, North Carolina 27403-6170, USA.

出版信息

J Cell Physiol. 2005 Jan;202(1):295-303. doi: 10.1002/jcp.20135.

Abstract

The colonic epithelium is often exposed to high concentrations of secondary bile acids, which stresses the epithelial cells, leading potentially to activation of stress-response genes. To examine this possibility in vitro, the purpose of this study was to determine if expression of certain growth arrest and DNA damage-inducible genes (GADD) is upregulated in human colonic epithelial cells exposed to deoxycholate (DOC). DNA macroarray screening of a small cluster of stress/apoptosis-related genes in DOC-treated HCT-116 colonocytes revealed clearly higher expression of only GADD45, which was confirmed by gene-specific relative RT-PCR analysis. Subsequently, it was found that DOC also increased GADD34 mRNA expression. However, mRNA expression of GADD153 was increased most markedly in DOC-treated HCT-116 colonocytes, which express wild-type p53. However, the upregulation of GADD34, GADD45, and GADD153 mRNA expression apparently did not require p53, based on the finding that DOC increased expression of all three GADD genes in HCT-15 colonocytes, which express mutant p53. In further studying GADD153 in particular, the effect of DOC on GADD153 mRNA was prevented by actinomycin-D (Act-D), but not by antioxidants or MAPK inhibitors. DOC also caused GADD153 protein to be expressed in close parallel with increased GADD153 mRNA expression. Induction of GADD153 protein by DOC was prevented by either anisomycin or cycloheximide. These findings suggest that DOC-induced upregulation of GADD153 mRNA expression occurred at the level of transcription without involving reactive oxygen species and MAPK signaling, and that the expression of GADD153 protein was due also to translation of pre-existing, and not just newly synthesized, mRNA.

摘要

结肠上皮经常暴露于高浓度的次级胆汁酸中,这会给上皮细胞造成压力,可能导致应激反应基因的激活。为了在体外研究这种可能性,本研究的目的是确定在暴露于脱氧胆酸盐(DOC)的人结肠上皮细胞中,某些生长停滞和DNA损伤诱导基因(GADD)的表达是否上调。对DOC处理的HCT-116结肠细胞中一小群应激/凋亡相关基因进行DNA微阵列筛选,结果清楚地显示只有GADD45的表达明显更高,这通过基因特异性相对RT-PCR分析得到了证实。随后发现,DOC也增加了GADD34 mRNA的表达。然而,在表达野生型p53的DOC处理的HCT-116结肠细胞中,GADD153的mRNA表达增加最为明显。然而,基于DOC增加了表达突变型p53的HCT-15结肠细胞中所有三种GADD基因的表达这一发现,GADD34、GADD45和GADD153 mRNA表达的上调显然不需要p53。特别是在进一步研究GADD153时,放线菌素-D(Act-D)可阻止DOC对GADD153 mRNA的影响,但抗氧化剂或MAPK抑制剂则不能。DOC还导致GADD153蛋白的表达与GADD153 mRNA表达的增加密切平行。茴香霉素或环己酰亚胺均可阻止DOC诱导的GADD153蛋白表达。这些发现表明,DOC诱导的GADD153 mRNA表达上调发生在转录水平,不涉及活性氧和MAPK信号传导,并且GADD153蛋白的表达也是由于预先存在的mRNA的翻译,而不仅仅是新合成的mRNA的翻译。

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