Literature DB >> 26426744

Temporal Profile of MicroRNA Expression in Contused Cortex after Traumatic Brain Injury in Mice.

Lilja Meissner1,2, Micaela Gallozzi1, Matilde Balbi1,2, Susanne Schwarzmaier1, Steffen Tiedt2, Nicole A Terpolilli3, Nikolaus Plesnila1,2,4.   

Abstract

MicroRNAs (miRNAs) were recently identified as important regulators of gene expression under a wide range of physiological and pathophysiological conditions. Thus, they may represent a novel class of molecular targets for the management of traumatic brain injury (TBI). In this study, we investigated the temporal profile of miRNA expression during the development of secondary brain damage after experimental TBI. For this purpose, we used a controlled cortical impact model in C57Bl/6 mice (n = 6) to induce a cortical contusion and analyzed miRNA expression in the traumatized cortex by microarray analysis during the development of secondary contusion expansion-i.e., at 1, 6, and 12 h after TBI. Of a total 780 mature miRNA sequences analyzed, 410 were detected in all experimental groups. Of these, 158 miRNAs were significantly upregulated or downregulated in TBI compared with sham-operated animals, and 52 miRNAs increased more than twofold. We validated the upregulation of five of the most differentially expressed miRNAs (miR-21*, miR-144, miR-184, miR-451, miR-2137) and the downregulation of four of the most differentially expressed miRNAs (miR-107, miR-137, miR-190, miR-541) by quantitative polymerase chain reaction (qPCR). miR-2137, the most differentially expressed miRNA after TBI, was further investigated by in situ hybridization and was found to be upregulated in neurons within the traumatic penumbra. This study gives a comprehensive picture of miRNA expression levels during secondary contusion expansion after TBI and may pave the way for the identification of novel targets for the management of brain trauma.

Entities:  

Keywords:  controlled cortical impact; miRNA; microarray; mouse; penumbra; traumatic brain injury

Mesh:

Substances:

Year:  2015        PMID: 26426744     DOI: 10.1089/neu.2015.4077

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  31 in total

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7.  Angiopoietin/Tie2 Axis Regulates the Age-at-Injury Cerebrovascular Response to Traumatic Brain Injury.

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10.  The microRNA miR-21 conditions the brain to protect against ischemic and traumatic injuries.

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