诱导糖尿病和手术模拟糖尿病缺血并发症在兔血液中发现的不同microrna。

Girish J Kotwal, Sabine Waigel, Julia Chariker, Eric Rouchka, Sufan Chien
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引用次数: 0

摘要

背景:近年来,糖尿病并发症得到了广泛的研究。由于缺乏已知的缺血特异性生物标志物,体液中很少有生物标志物可以精确定位明显的糖尿病并发症。目的:在动物模型中鉴定每种并发症的microRNA,如果在人类中得到证实,可以早期诊断给定的并发症。MicroRNA (miRNA)谱分析已经在啮齿动物模型中完成了许多糖尿病并发症,如糖尿病肾小球损伤、动脉粥样硬化、认知障碍、糖尿病伤口愈合、血管病变和其他并发症。由于啮齿类动物和人类之间存在多种差异,兔子皮肤的变化被认为比猪更接近人类,可能更好地模拟人类糖尿病缺血并发症。方法:研究糖尿病或手术致缺血家兔的miRNA谱,研究是否能检测到糖尿病或缺血诱导的特异性miRNA。从糖尿病家兔和局部缺血家兔的血液中采集MicroRNA,用专门设计的PAXgene血液RNA管分离miRNA,用PAX基因miRNA提取试剂盒提取。利用RNA分析仪对分离的RNA进行质量控制,并利用RNA seq技术分析在缺血诱导的糖尿病和非糖尿病家兔中检测到的不同miRNAs。结果:在糖尿病家兔和缺血家兔中有表达,而在未治疗家兔中无表达的miRNA-183。几个mirna在对照组中表达差异,并且在每个比较中鉴定出几个上调的mirna是独特的。在长期缺血模型的潜在糖尿病并发症家兔中,有一种独特的microRNA在缺血家兔中高度显著上调(miRNA-133-3p)。有一个miRNA-3074-5p在糖尿病家兔中显著上调,而在缺血家兔中没有上调。只有统计上显著的结果才被考虑和分析。结论:这些发现可以在没有侵入性组织活检的情况下准确及时地诊断潜在的单一糖尿病并发症,并可能成为管理因糖尿病进展而出现并发症的糖尿病患者的新工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distinct MicroRNAs Identified in Rabbit Blood Arising from Induced Diabetes and a Surgically Simulated Diabetic Ischemia Complication.

Background: Diabetic complications have been studied extensively in recent years. There are very few biomarkers in body fluids that can pinpoint a distinct diabetic complication due to insufficient known specific biomarkers for ischemia.

Objective: Identifying microRNA in animal models for each complication could enable early diagnosis of a given complication if verified in humans. MicroRNA (miRNA) profiling has been done in rodent models for a number of diabetic complications, like diabetic glomerular injury, atherosclerosis, cognitive impairment, diabetic wound healing, angiopathy and other complications. Due to multiple differences between rodents and humans, the changes in rabbit skin, considered closer to humans than even pigs, may better simulate human diabetic complications of ischemia.

Methods: To study the miRNA profile of rabbits in which diabetes was induced or ischemia was surgically generated, we studied whether diabetes or ischemia-induced specific miRNA could be detected. MicroRNA from the blood of diabetic rabbits and rabbits with local ischemia was collected in PAXgene Blood RNA tubes specifically designed for miRNA isolation and extracted using the PAX gene miRNA extraction kit. The isolated RNA was quality controlled using an RNA analyzer, and further, using RNA seq technology, it was analyzed for distinct miRNAs that were detected in diabetic and non-diabetic rabbits induced with ischemia.

Results: A miRNA that was found to be expressed in diabetic rabbits and ischemic rabbits but not in untreated rabbits was miRNA-183. Several miRNAs were differentially expressed across comparison groups, and several upregulated miRNAs were identified being unique to each comparison. In rabbits with a potential diabetic complication of a long-term ischemic model, there was one distinct microRNA, which was highly significantly upregulated in ischemia rabbit (miRNA-133-3p). One miRNA that was highly significantly upregulated in diabetic rabbit but not in ischemic rabbits was miRNA-3074-5p. Only statistically significant results have been considered and analyzed.

Conclusion: These findings could lead to a precise and timely diagnosis of a potential single diabetic complication without invasive tissue biopsies and could be a novel tool in the management of diabetic patients developing complications due to the progression of diabetes.

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