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Estimation of time-dependent microRNA expression patterns in brain tissue,leukocytes, and blood plasma of rats under photochemically induced focal cerebral ischemia
Authors:Email author" target="_blank">V?A?GusarEmail author  A?V?Timofeeva  I?S?Zhanin  S?I?Shram  V?G?Pinelis
Institution:1.Kulakov Research Center for Obstetrics, Gynecology, and Perinatology,Ministry of Healthcare of the Russian Federation,Moscow,Russia;2.Scientific Center of Children’s Health,Ministry of Healthcare of the Russian Federation,Moscow,Russia;3.Sechenov First Moscow State Medical University,Moscow,Russia;4.Institute of Molecular Genetics,Russian Academy of Sciences,Moscow,Russia
Abstract: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.
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