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谷氨酰胺对肠道上皮细胞的保护作用:诱导型热休克蛋白70的作用

Glutamine protects intestinal epithelial cells: role of inducible HSP70.

作者信息

Wischmeyer P E, Musch M W, Madonna M B, Thisted R, Chang E B

机构信息

Department of Medicine, University of Chicago, Illinois 60637, USA.

出版信息

Am J Physiol. 1997 Apr;272(4 Pt 1):G879-84. doi: 10.1152/ajpgi.1997.272.4.G879.

Abstract

Glutamine (Gln) protects gut mucosa against injury and promotes mucosal healing. Because the induction of heat shock proteins (HSP) protects cells under conditions of stress, we determined whether Gln conferred protection against stress in an intestinal epithelial cell line through HSP induction. Gln added to IEC-18 cells induces an increase in HSP70, a concentration-dependent effect also seen with mRNA. Two forms of injury, lethal heat (49 degrees C) and oxidant, were used, and viability was determined by 51Cr release. Gln-treated cells were significantly more resistant to injury. Treatment with 6-diazo-5-oxo-L-norleucine (DON), a nonmetabolizable analog of Gln, induced HSP70 and protected cells from injury, but less than Gln. These findings suggest that the effects of Gln on HSP70 induction and cellular protection are mediated by metabolic and nonmetabolic mechanisms. To determine whether HSP induction was central to the action of Gln and DON, quercetin, which blocks HSP induction, was used. Quercetin blocked HSP70 induction and the protective effect of Gln and DON. We conclude that the protective effects of Gln in intestinal epithelial cells are in part mediated by HSP70 induction.

摘要

谷氨酰胺(Gln)可保护肠道黏膜免受损伤并促进黏膜愈合。由于热休克蛋白(HSP)的诱导可在应激条件下保护细胞,我们研究了Gln是否通过诱导HSP来保护肠上皮细胞系免受应激。添加到IEC - 18细胞中的Gln可诱导HSP70增加,mRNA也呈现浓度依赖性效应。使用了两种损伤形式,致死性热(49摄氏度)和氧化剂,并通过51Cr释放来测定细胞活力。经Gln处理的细胞对损伤的抵抗力明显更强。用6 - 重氮 - 5 - 氧代 - L - 正亮氨酸(DON)(Gln的一种不可代谢类似物)处理可诱导HSP70并保护细胞免受损伤,但效果不如Gln。这些发现表明,Gln对HSP70诱导和细胞保护的作用是由代谢和非代谢机制介导的。为了确定HSP诱导是否是Gln和DON作用的核心,使用了可阻断HSP诱导的槲皮素。槲皮素阻断了HSP70的诱导以及Gln和DON的保护作用。我们得出结论,Gln在肠上皮细胞中的保护作用部分是由HSP70诱导介导的。

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