首页> 外文期刊>Apoptosis: An international journal on programmed cell death >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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The purpose of the present study was to evaluate the effect of transforming-growth factor-alpha (TGF-alpha) 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-alpha. Cell apoptosis was determined by FACS cytometry. Adult rats were divided into four groups: Control, Control-TGF-alpha, MTX, and MTX- TGF-alpha 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-alpha 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-alpha 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-alpha on enterocyte apoptosis was strongly correlated with EGFr expression along the villus-crypt axis. In conclusion, treatment with TGF-alpha 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,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的Caco-2细胞进行治疗会以剂量依赖的方式显着抑制细胞凋亡。在体内实验中,MTX-TGF-α大鼠的凋亡水平下降与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。

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