Department of Medicine, Stony Brook University, Stony Brook, New York; and.
Department of Gastroenterology, the Affiliated Hospital of Ningbo University School of Medicine, Ningbo, China.
Am J Physiol Gastrointest Liver Physiol. 2015 Jan 15;308(2):G121-38. doi: 10.1152/ajpgi.00080.2014. Epub 2014 Nov 20.
Gut radiation-induced injury is a concern during treatment of patients with cancer. Krüppel-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 γ-irradiation in vitro. We sought to determine whether KLF4 mediates the small intestinal response to γ-irradiation in vivo. Mice with intestinal epithelium-specific deletion of Klf4 (Klf4(ΔIS)) and control (Klf4(fl/fl)) mice were irradiated with total-body γ-radiation. Following irradiation, the Klf4(ΔIS) mice had significantly increased mortality compared with irradiated Klf4(fl/fl) mice. Immunohistochemistry 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 Klf4(ΔIS) 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 Klf4(ΔIS) mice had a significantly higher number of crypt cells positive for apoptosis, p53, and p21 compared with irradiated Klf4(fl/fl) mice. Taken together, our data suggest that Klf4 may function as a radioprotective factor against gastrointestinal syndrome in mice following γ-irradiation by inhibiting apoptosis in the acute response to irradiation and contributing to crypt regeneration.
肠道辐射损伤是癌症患者治疗过程中的一个关注点。Krüppel 样因子 4(KLF4)在小肠分化的绒毛状上皮细胞中表达。我们之前的研究表明,KLF4 可保护细胞免受体外γ辐射诱导的凋亡。我们试图确定 KLF4 是否介导体内γ辐射对小肠的反应。具有肠上皮细胞特异性缺失 Klf4(Klf4(ΔIS))的小鼠和对照(Klf4(fl/fl))小鼠接受全身γ辐射照射。照射后,Klf4(ΔIS) 小鼠的死亡率明显高于照射的 Klf4(fl/fl) 小鼠。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、增殖水平和凋亡。照射后 96 小时,两种小鼠均出现再生反应,表现为增殖带扩张,对照组的增殖活性高于 Klf4(ΔIS)组。此外,与未照射的小鼠相比,照射后的对照小鼠中 Klf4/Ki67 共阳性细胞的数量显著增加。此外,与照射的 Klf4(fl/fl) 小鼠相比,照射的 Klf4(ΔIS) 小鼠中 p53 和 p21 阳性的隐窝细胞数量明显增加。总之,我们的数据表明,Klf4 可能通过抑制辐射急性反应中的凋亡并有助于隐窝再生,从而在 γ 辐射照射后作为一种针对小鼠胃肠道综合征的放射保护因子发挥作用。