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首页> 外文期刊>American Journal of Physiology >Kriippel-like factor 4 is a radioprotective factor for the intestine following gamma-radiation-induced gut injury in mice
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Kriippel-like factor 4 is a radioprotective factor for the intestine following gamma-radiation-induced gut injury in mice

机译:Krippel样因子4是γ-辐射诱导的小鼠肠道诱导后肠道的放射性保护因子

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摘要

Gut radiation-induced injury is a concern during treatment of patients with cancer. Kriippel-like factor 4 (KLF4) is expressed in differentiated villous epithelial cells of the small intestine. We previously showed that KLF4 protects cells from apoptosis following 7-irradiation in vitro. We sought to determine whether KLF4 mediates the small intestinal response to 7-irradiation in vivo. Mice with intestinal epithelium-specific deletion of Klf4 (Klj4AIS) and control {JZ.lf4fUft) mice were irradiated with total-body 7-radiation. Following irradiation, the Klf4MS mice had significantly increased mortality compared with irradiated Klf4W mice. Immuno-histochemistry and immunofluorescence staining were used to assess the morphological changes, levels of proliferation, and apoptosis in the intestinal epithelium. At 96 h following irradiation, there was a regenerative response manifested by an expansion of the proliferative zone in both mouse groups, with the control mice having a higher proliferative activity than the Klf4Ars group. In addition, there was a significant increase in the number of Klf4/Ki67-copositive cells in the irradiated control mice compared with unirradiated mice. Also, the irradiated Klf4AIS mice had a significantly higher number of crypt cells pQsitive for apoptosis, p53, and p21 compared with irradiated KlfflW mice. Taken together, our data suggest that Klf4 may function as a radioprotective factor against gastrointestinal syndrome in mice following 7-irradiation by inhibiting apoptosis in the acute response to irradiation and contributing to crypt regeneration.
机译:肠道辐射诱导的损伤是治疗癌症患者期间的疑虑。 Krippel样因子4(KLF4)在小肠的差异化绒毛上皮细胞中表达。我们以前表明KLF4在体外7辐射后保护细胞免受细胞凋亡。我们试图确定KLF4是否介导对体内7辐射的小肠反应。用全身7-辐射照射具有肠道上皮细胞特异性缺失的KLF4(KLJ4AIS)和对照{JZ.LF4FUFFT)小鼠。在照射后,与辐照的KLF4W小鼠相比,KLF4MS小鼠的死亡率显着增加。免疫组织化学和免疫荧光染色用于评估肠上皮细胞的形态变化,增殖水平和细胞凋亡。在96小时后照射后,在两种小鼠基团中的增殖区的扩增具有再生响应,对照小鼠具有比KLF4ARS组更高的增殖活性。另外,与未照射的小鼠相比,辐照对照小鼠中的KLF4 / Ki67 - 连体细胞的数量显着增加。此外,与辐照的KLFFLW小鼠相比,辐照的KLF4AIS小鼠对细胞凋亡,P53和P21具有显着较高的隐窝细胞PQSINT。我们的数据表明,通过抑制急性反应的辐照和促成隐窝再生,KLF4可以用作小鼠胃肠道综合征的放射性保护因子。

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