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组蛋白甲基化抑制剂DZNep通过抑制TIM-1介导的T细胞活化改善肾缺血再灌注损伤。

Histone Methylation Inhibitor DZNep Ameliorated the Renal Ischemia-Reperfusion Injury Inhibiting TIM-1 Mediated T Cell Activation.

作者信息

Li Jiawei, Qiu Yue, Li Long, Wang Jiyan, Cheuk Yin Celeste, Sang Ruirui, Jia Yichen, Wang Jina, Zhang Yi, Rong Ruiming

机构信息

Department of Urology, Zhongshan Hospital, Fudan University, Shanghai, China.

Shanghai Key Laboratory of Organ Transplantation, Shanghai, China.

出版信息

Front Med (Lausanne). 2020 Jul 10;7:305. doi: 10.3389/fmed.2020.00305. eCollection 2020.

Abstract

Renal ischemia-reperfusion injury (IRI) after renal transplantation often leads to the loss of kidney graft function. However, there is still a lack of efficient regimens to prevent or alleviate renal IRI. Our study focused on the renoprotective effect of 3-Deazaneplanocin A (DZNep), which is a histone methylation inhibitor. We found that DZNep significantly alleviated renal IRI by suppressing nuclear factor kappa-B (NF-κB), thus inhibiting the expression of inflammatory factors in renal tubular epithelial cells or . After treatment with DZNep, T cell activation was impaired in the spleen and kidney, which correlated with the downregulated expression of T-cell immunoglobulin mucin (TIM)-1 on T cells and TIM-4 in macrophages. In addition, pretreatment with DZNep was not sufficient to protect the kidney, while administration of DZNep from before to after surgery significantly ameliorated IRI. Our findings suggest that DZNep can be a novel strategy for preventing renal IRI following kidney transplantation.

摘要

肾移植后的肾缺血再灌注损伤(IRI)常导致肾移植肾功能丧失。然而,目前仍缺乏预防或减轻肾IRI的有效方案。我们的研究聚焦于3-脱氮杂氮胞苷A(DZNep)的肾脏保护作用,它是一种组蛋白甲基化抑制剂。我们发现,DZNep通过抑制核因子κB(NF-κB)显著减轻肾IRI,从而抑制肾小管上皮细胞中炎症因子的表达。用DZNep治疗后,脾脏和肾脏中的T细胞活化受损,这与T细胞上T细胞免疫球蛋白粘蛋白(TIM)-1和巨噬细胞中TIM-4表达下调有关。此外,术前用DZNep预处理不足以保护肾脏,而术前至术后给予DZNep可显著改善IRI。我们的研究结果表明,DZNep可能是预防肾移植后肾IRI的一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0077/7365856/a2257da5aa8c/fmed-07-00305-g0001.jpg

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