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新型 miRNA PC-5P-12969 与缺血性脑卒中。

Novel miRNA PC-5P-12969 in Ischemic Stroke.

机构信息

Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA.

Department of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.

出版信息

Mol Neurobiol. 2019 Oct;56(10):6976-6985. doi: 10.1007/s12035-019-1562-x. Epub 2019 Apr 5.

Abstract

Circulating microRNAs (miRNAs) have been used effectively as peripheral biomarkers and mechanistic targets for human diseases such as stroke, Alzheimer's, and cancer. The purpose of our study is to determine noninvasive, blood-based early detectable biomarkers for ischemic stroke (IS). Based on our previous global miRNA sequencing study, four miRNAs were previously unreported (novel) in IS condition. Among these, miRNA PC-5P-12969 was exclusively expressed in the IS condition; otherwise, it was not expressed in normal condition, and therefore, we focused on miRNA PC-5P-12969 for further studies. In the present study, we investigated novel miRNA PC-5P-12969 for its expression levels using quantitative real-time PCR assay (qRT-PCR) in an in vitro, oxygen, and glucose deprivation/reoxygenation (OGD/R)-treated mouse primary hippocampal neuronal cells (HT22) and in an in vivo using a photothrombotic stroke model. In an in vitro study of stroke-induced HT22 cells, we found a two fold increase of PC-5P-12969 expression levels, in agreement with our original global miRNA study. In the cerebral cortex of photothrombotic stroke mice, we found significantly upregulated levels of PC-5P-12969 in 4 hours and 1 day post-stroke relative to the control mice. However, we did not find any change in the expression of PC-5P-12969 in the cerebellum (unaffected in IS) of both stroke and control mice. Based on findings from this study, together with our earlier original global microRNA study results, we conclude that PC-5P-12969 is a potential candidate of the peripheral marker and also a drug target for IS. This is the first study validating that the miRNA PC-5P-12969, might be a potential biomarker for IS.

摘要

循环 microRNAs(miRNAs)已被有效地用作中风、阿尔茨海默病和癌症等人类疾病的外周生物标志物和机制靶点。我们研究的目的是确定缺血性中风(IS)的非侵入性、基于血液的早期可检测生物标志物。基于我们之前的全球 miRNA 测序研究,有 4 个 miRNA 在 IS 情况下以前未被报道(新颖)。在这些 miRNA 中,miRNA PC-5P-12969 仅在 IS 情况下表达;否则,在正常情况下不表达,因此,我们专注于 miRNA PC-5P-12969 进行进一步研究。在本研究中,我们使用定量实时 PCR assay(qRT-PCR)在体外、氧和葡萄糖剥夺/复氧(OGD/R)处理的小鼠原代海马神经元细胞(HT22)和体内使用光血栓性中风模型研究了新型 miRNA PC-5P-12969 的表达水平。在中风诱导的 HT22 细胞的体外研究中,我们发现 PC-5P-12969 的表达水平增加了两倍,这与我们最初的全球 miRNA 研究一致。在光血栓性中风小鼠的大脑皮质中,我们发现与对照组相比,中风后 4 小时和 1 天 PC-5P-12969 水平显著上调。然而,我们没有发现中风和对照组小鼠小脑(不受 IS 影响)中 PC-5P-12969 表达的任何变化。基于这项研究的结果以及我们之前的原始全球 microRNA 研究结果,我们得出结论,PC-5P-12969 是外周标志物的潜在候选物,也是 IS 的药物靶点。这是第一项验证 miRNA PC-5P-12969 可能是 IS 潜在生物标志物的研究。

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