首页> 外文期刊>Apoptosis >Effect of transforming growth factor-alpha on enterocyte apoptosis is correlated with EGF receptor expression along the villus-crypt axis during methotrexate-induced intestinal mucositis in a rat
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Effect of transforming growth factor-alpha on enterocyte apoptosis is correlated with EGF receptor expression along the villus-crypt axis during methotrexate-induced intestinal mucositis in a rat

机译:甲氨蝶呤致大鼠肠黏膜炎期间转化生长因子-α对肠细胞凋亡的影响与绒毛隐窝轴上EGF受体的表达相关

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摘要

The purpose of the present study was to evaluate the effect of transforming-growth factor-alpha (TGF-α) on enterocyte apoptosis following methotrexate (MTX) induced intestinal mucositis in a rat and in Caco-2 cells. Non-pretreated and pretreated with MTX Caco-2 cells were incubated with increasing concentrations of TGF-α. Cell apoptosis was determined by FACS cytometry. Adult rats were divided into four groups: Control, Control-TGF-α, MTX, and MTX- TGF-α rats. Three days later rats were sacrificed. Enterocyte apoptosis were measured at sacrifice. RT-PCR and Western Blotting was used to determine the level of Bax and Bcl-2 mRNA and protein. Real time PCR was used to measure epidermal growth factor receptor (EGFr) expression along the villus-crypt axis. The in vitro experiment has shown that treatment with TGF-α of Caco-2 cells results in a significant inhibition of cell apoptosis in a dose-dependent manner. In vivo experiment, a decreased levels of apoptosis in MTX- TGF-α rats corresponded with the decrease in Bax and with the increase in Bcl-2 at both mRNA and protein levels. The inhibiting effect of TGF-α on enterocyte apoptosis was strongly correlated with EGFr expression along the villus-crypt axis. In conclusion, treatment with TGF-α inhibits enterocyte apoptosis following MTX- injury in the rat.
机译:本研究的目的是评估转化生长因子-α(TGF-α)对甲氨蝶呤(MTX)诱导的大鼠和Caco-2细胞肠粘膜炎后肠细胞凋亡的影响。将未经预处理和经MTX Caco-2细胞预处理过的TGF-α浓度增加。通过FACS细胞计数法测定细胞凋亡。成年大鼠分为四组:对照组,对照-TGF-α,MTX和MTX-TGF-α大鼠。三天后,处死大鼠。处死时测量肠细胞凋亡。用RT-PCR和蛋白质印迹法测定Bax和Bcl-2 mRNA和蛋白质的水平。实时PCR被用于测量沿绒毛-隐窝轴的表皮生长因子受体(EGFr)表达。体外实验表明,用TGF-α处理Caco-2细胞可显着抑制细胞凋亡,并呈剂量依赖性。在体内实验中,MTX-TGF-α大鼠的凋亡水平降低与mRNA和蛋白质水平上的Bax降低和Bcl-2升高相对应。 TGF-α对肠细胞凋亡的抑制作用与沿绒毛-隐窝轴的EGFr表达高度相关。总之,用TGF-α处理可抑制大鼠MTX损伤后肠细胞的凋亡。

著录项

  • 来源
    《Apoptosis》 |2008年第11期|1344-1355|共12页
  • 作者单位

    Laboratory of intestinal adaptation and recovery The Bruce Rappaport Faculty of Medicine Technion-Israel Institute of Technology Haifa Israel;

    Laboratory of intestinal adaptation and recovery The Bruce Rappaport Faculty of Medicine Technion-Israel Institute of Technology Haifa Israel;

    Laboratory of intestinal adaptation and recovery The Bruce Rappaport Faculty of Medicine Technion-Israel Institute of Technology Haifa Israel;

    Laboratory of intestinal adaptation and recovery The Bruce Rappaport Faculty of Medicine Technion-Israel Institute of Technology Haifa Israel;

    Department of Pediatric Surgery Bnai Zion Medical Center 47 Golomb St. P. O. Box 4940 31048 Haifa Israel;

    Department of Pediatric Surgery Hannover Medical School Hannover Germany;

    Department of Pediatric Surgery Bnai Zion Medical Center 47 Golomb St. P. O. Box 4940 31048 Haifa Israel;

    Section of Pediatric Surgery C.S Mott Children’s Hospital and University of Michigan Medical School Ann Arbor MI USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Methotrexate; Intestine; TGF-α; EGFr; Enterocyte proliferation; Enterocyte apoptosis;

    机译:甲氨蝶呤;肠;TGF-α;EGFr;肠细胞增殖;肠细胞凋亡;

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