Estimation of Time-Dependent microRNA Expression Patterns in Brain Tissue, Leukocytes, and Blood Plasma of Rats under Photochemically Induced Focal Cerebral Ischemia

被引:0
|
作者
Gusar, V. A. [1 ,2 ]
Timofeeva, A. V. [1 ,2 ]
Zhanin, I. S. [2 ,3 ]
Shram, S. I. [4 ]
Pinelis, V. G. [2 ]
机构
[1] Minist Healthcare Russian Federat, Kulakov Res Ctr Obstet Gynecol & Perinatol, Moscow 117997, Russia
[2] Minist Healthcare Russian Federat, Sci Ctr Childrens Hlth, Moscow 119991, Russia
[3] Sechenov First Moscow State Med Univ, Moscow 119991, Russia
[4] Russian Acad Sci, Inst Mol Genet, Moscow 123182, Russia
基金
俄罗斯基础研究基金会;
关键词
microRNA; cerebral ischemia; neuronal damage; leukocytes; photochemically induced cerebral ischemia; deep sequencing; real-time quantitative PCR; PHOTOTHROMBOTIC RING STROKE; GENE-EXPRESSION; REPERFUSION INJURY; MONONUCLEAR-CELLS; TEMPORAL-CHANGES; ACCUMULATION; REGIONS; PROFILE; TARGET; MODEL;
D O I
10.1134/S0026893317040100
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
miRNA expression over different time periods (24 and 48 h) using the quantitative RT-PCR and deep sequencing has been evaluated in a model of photochemically induced thrombosis. A combination of two approaches allowed us to determine the miRNA expression patterns caused by ischemia. Nine miRNAs, including let-7f-5p, miR-221-3p, miR-21-5p, miR-30c-5p, miR-30a-3p, miR-223-3p, miR-23a-3p, miR-22-5p, and miR-99a-5p, were differentially expressed in brain tissue and leukocytes of rats 48 h after onset of ischemia. In addition, six miRNAs were differentially expressed in the brain tissue and blood plasma of rats 24 h after exposure, among which miR-145-3p and miR-375-3p were downregulated and miR-19a-3p, miR-92a-3p, miR-188-5p, and miR-532-5p were upregulated. In our opinion, miR-188-5p and miR-532-5p may be considered to be new potential markers of ischemic injury. The level of miRNA expression tended to increase 48 h after the onset of ischemia in brain tissue and leukocytes, which reflects not only the local response in brain tissue due to inflammation, vascular endothelial dysfunction, and disorders of the permeability of the blood-brain barrier, but also the systemic response of the organism to multifactor molecular processes induced by ischemic injury.
引用
收藏
页码:602 / 613
页数:12
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