Expression of miRNAs and Their Cooperative Regulation of the Pathophysiology in Traumatic Brain Injury

被引:47
作者
Hu, Zhonghua [1 ]
Yu, Danni [4 ]
Almeida-Suhett, Camila [5 ]
Tu, Kang [3 ]
Marini, Ann M. [6 ]
Eiden, Lee [2 ]
Braga, Maria F. [5 ]
Zhu, Jun [3 ]
Li, Zheng [1 ]
机构
[1] NIMH, Unit Synapse Dev & Plast, NIH, Bethesda, MD 20892 USA
[2] NIMH, Lab Cellular & Mol Regulat, NIH, Bethesda, MD 20892 USA
[3] NHLBI, Genet & Dev Biol Ctr, NIH, Bethesda, MD 20892 USA
[4] Purdue Univ, Dept Stat, W Lafayette, IN 47907 USA
[5] Uniformed Serv Univ Hlth Sci, Sch Med, Dept Anat Physiol & Genet, Bethesda, MD 20814 USA
[6] Uniformed Serv Univ Hlth Sci, Sch Med, Dept Neurol, Bethesda, MD 20814 USA
来源
PLOS ONE | 2012年 / 7卷 / 06期
关键词
GENE-EXPRESSION; MICRORNA; IMPACT; RAT; NEUROPROTECTION; MECHANISMS; GENOME; MEMORY;
D O I
10.1371/journal.pone.0039357
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Traumatic brain injury (TBI) is a leading cause of injury-related death and disability worldwide. Effective treatment for TBI is limited and many TBI patients suffer from neuropsychiatric sequelae. The molecular and cellular mechanisms underlying the neuronal damage and impairment of mental abilities following TBI are largely unknown. Here we used the next generation sequencing platform to delineate miRNA transcriptome changes in the hippocampus at 24 hours and 7 days following TBI in the rat controlled cortical impact injury (CCI) model, and developed a bioinformatic analysis to identify cellular activities that are regulated by miRNAs differentially expressed in the CCI brains. The results of our study indicate that distinct sets of miRNAs are regulated at different post-traumatic times, and suggest that multiple miRNA species cooperatively regulate cellular pathways for the pathological changes and management of brain injury. The distinctive miRNAs expression profiles at different post-CCI times may be used as molecular signatures to assess TBI progression. In addition to known pathophysiological changes, our study identifies many other cellular pathways that are subjected to modification by differentially expressed miRNAs in TBI brains. These pathways can potentially be targeted for development of novel TBI treatment.
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页数:11
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