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肾盂肾炎大鼠模型中肾瘢痕形成的全基因组表达谱分析。

Global gene expression profiling of renal scarring in a rat model of pyelonephritis.

作者信息

Ichino Manabu, Mori Terumi, Kusaka Mamoru, Kuroyanagi Yoko, Ishikawa Kiyohito, Shiroki Ryoichi, Kowa Hiroe, Kurahashi Hiroki, Hoshinaga Kiyotaka

机构信息

Department of Urology, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, Japan.

出版信息

Pediatr Nephrol. 2008 Jul;23(7):1059-71. doi: 10.1007/s00467-007-0717-6. Epub 2008 Jan 23.

Abstract

Renal scarring is a serious complication of chronic pyelonephritis that occurs due to vesicoureteral reflux. In our study, we performed global expression profiling of the kidney during renal scarring formation in a rat pyelonephritis model. An inoculum of Escherichia coli was injected directly into the renal cortex. Histologically, renal scarring developed during the 3-to-4 week period after injection. The time-course expression profile of 18,442 genes was then analyzed using microarrays, followed by validation with real-time reverse transcriptase-polymerase chain reaction (RT-PCR). Most of the genes found to be up-regulated during renal scarring are associated with immune and defense responses, including cytokines, chemokines and their receptors, complement factors, adhesion molecules and extracellular matrix proteins. These genes were up-regulated as early as 1 week after injection, when no fibrotic changes were yet evident, peaked at 2 weeks, and gradually decreased thereafter. However, a subset of cytokine genes was found to be persistently activated even at 6 weeks after injection, including interleukin (IL)-1beta, transforming growth factor (TGF)-beta, and IL-3. Further statistical analysis indicated that the pathways mediated by these cytokines are activated concomitantly with renal scarring formation. The products of these genes may thus potentially be novel non-invasive diagnostic or prognostic biomarkers of renal scarring.

摘要

肾瘢痕形成是慢性肾盂肾炎的一种严重并发症,其由膀胱输尿管反流引起。在我们的研究中,我们在大鼠肾盂肾炎模型的肾瘢痕形成过程中对肾脏进行了全基因组表达谱分析。将大肠杆菌接种物直接注入肾皮质。组织学上,肾瘢痕在注射后3至4周内形成。然后使用微阵列分析18442个基因的时间进程表达谱,随后用实时逆转录聚合酶链反应(RT-PCR)进行验证。在肾瘢痕形成过程中发现上调的大多数基因与免疫和防御反应相关,包括细胞因子、趋化因子及其受体、补体因子、黏附分子和细胞外基质蛋白。这些基因在注射后1周就开始上调,此时尚无明显的纤维化改变,在2周时达到峰值,此后逐渐下降。然而,发现即使在注射后6周,一部分细胞因子基因仍持续激活,包括白细胞介素(IL)-1β、转化生长因子(TGF)-β和IL-3。进一步的统计分析表明,由这些细胞因子介导的通路与肾瘢痕形成同时被激活。因此,这些基因的产物可能是肾瘢痕形成的新型非侵入性诊断或预后生物标志物。

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