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TLR4 Agonist Monophosphoryl Lipid A Alleviated Radiation-Induced Intestinal Injury

机译:TLR4激动剂单磷虾脂质缓解辐射诱导的肠损伤

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The small intestine is one of the most sensitive organs to irradiation injury, and the development of high effective radioprotectants especially with low toxicity for intestinal radiation sickness is urgently needed. Monophosphoryl lipid A (MPLA) was found to be radioprotective in our previous study, while its effect against the intestinal radiation injury remained unknown. In the present study, we firstly determined the intestinal apoptosis after irradiation injury according to the TUNEL assay. Subsequently, we adopted the immunofluorescence technique to assess the expression levels of different biomarkers including Ki67, γ-H2AX, and defensin 1 in vivo. Additionally, the inflammatory cytokines were detected by RT-PCR. Our data indicated that MPLA could protect the intestine from ionizing radiation (IR) damage through activating TLR4 signal pathway and regulating the inflammatory cytokines. This research shed new light on the protective effect of the novel TLR4 agonist MPLA against intestine detriment induced by IR.
机译:小肠是迫害损伤最敏感的器官之一,迫切需要开发高有效的辐射保护剂,尤其是对肠道辐射疾病的低毒性。在我们以前的研究中发现单磷虾脂质A(MPLA)是放射性保护,而其对肠道抗损伤的影响仍然是未知的。在本研究中,根据TUNEL测定,我们首先确定了辐照损伤后的肠道凋亡。随后,我们采用免疫荧光技术来评估不同生物标志物的表达水平,包括ki67,γ-h2ax和defensin 1的体内。另外,通过RT-PCR检测炎性细胞因子。我们的数据表明,MPLA可以通过激活TLR4信号途径和调节炎性细胞因子来保护肠道电离辐射(IR)损伤。这项研究揭示了新的TLR4激动剂MPLA对IR诱导肠毒死率的保护作用。

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