肌痛性脑脊髓炎/慢性疲劳综合征运动诱导的脑通路调节的信息学推断。

Network and systems medicine Pub Date : 2020-11-18 eCollection Date: 2020-01-01 DOI:10.1089/nsm.2019.0009
Vaishnavi Narayan, Narayan Shivapurkar, James N Baraniuk
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引用次数: 1

摘要

引言:肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)的运动后不适是通过比较没有运动和次最大运动的受试者脑脊液中的微小RNA(miRNA)来建模的。材料和方法:通过信息学方法检测差异表达的miRNA,以预测运动影响的潜在靶点和调节途径。结果:与腰椎穿刺前运动的受试者(n=15)相比,休息过夜(非运动组n=45)的受试对象的miR-608、miR-328、miR-200a-5p、miR-93-3p和miR-92a-3p水平更高。在DIANA MiRpath v3.0、TarBase、Cytoscape和Ingenuity软件®中检测该组合,以选择靶mRNA的交叉点。DIANA发现33个运动后可能升高的靶点,包括TGFBR1、IGFR1和CDC42。粘附和粘附连接是最常见的途径。Ingenuity选择了七个具有互补机制途径的靶标,涉及GNAQ、ADCY3、RAP1B和PIK3R3。表达高水平这些基因的潜在靶细胞包括脉络丛、神经元和小胶质细胞。结论:运动后脑脊液中这种miRNA组合的减少表明,在脑脊髓炎/慢性疲劳综合征运动后不适期间,磷酸肌醇信号通路上调,粘附性改变。临床试验注册号:NCT01291758和NCT00810225。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Informatics Inference of Exercise-Induced Modulation of Brain Pathways Based on Cerebrospinal Fluid Micro-RNAs in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

Informatics Inference of Exercise-Induced Modulation of Brain Pathways Based on Cerebrospinal Fluid Micro-RNAs in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

Informatics Inference of Exercise-Induced Modulation of Brain Pathways Based on Cerebrospinal Fluid Micro-RNAs in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

Informatics Inference of Exercise-Induced Modulation of Brain Pathways Based on Cerebrospinal Fluid Micro-RNAs in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

Introduction: The post-exertional malaise of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) was modeled by comparing micro-RNA (miRNA) in cerebrospinal fluid from subjects who had no exercise versus submaximal exercise. Materials and Methods: Differentially expressed miRNAs were examined by informatics methods to predict potential targets and regulatory pathways affected by exercise. Results: miR-608, miR-328, miR-200a-5p, miR-93-3p, and miR-92a-3p had higher levels in subjects who rested overnight (nonexercise n=45) compared to subjects who had exercised before their lumbar punctures (n=15). The combination was examined in DIANA MiRpath v3.0, TarBase, Cytoscape, and Ingenuity software® to select the intersection of target mRNAs. DIANA found 33 targets that may be elevated after exercise, including TGFBR1, IGFR1, and CDC42. Adhesion and adherens junctions were the most frequent pathways. Ingenuity selected seven targets that had complementary mechanistic pathways involving GNAQ, ADCY3, RAP1B, and PIK3R3. Potential target cells expressing high levels of these genes included choroid plexus, neurons, and microglia. Conclusion: The reduction of this combination of miRNAs in cerebrospinal fluid after exercise suggested upregulation of phosphoinositol signaling pathways and altered adhesion during the post-exertional malaise of ME/CFS. Clinical Trial Registration Nos.: NCT01291758 and NCT00810225.

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