Identifying the role of microRNAs in spinal cord injury

被引:35
作者
Dong, Jun [1 ]
Lu, Meng [1 ]
He, Xijing [1 ]
Xu, Junkui [2 ]
Qin, Jie [1 ]
Cheng, Zhijian [1 ]
Liang, Baobao [3 ]
Wang, Dong [1 ]
Li, Haopeng [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Orthoped, Affiliated Hosp 2, Xian 710004, Peoples R China
[2] Xi An Jiao Tong Univ, Dept Orthoped, Honghui Hosptial, Xian 710054, Peoples R China
[3] Xi An Jiao Tong Univ, Dept Plast Surg, Affiliated Hosp 2, Xian 710004, Peoples R China
关键词
Spinal cord injury; MicroRNA; Pathophysiology; CENTRAL-NERVOUS-SYSTEM; NEURAL PLASTICITY; POSTTRANSCRIPTIONAL REGULATION; ISCHAEMIA/REPERFUSION INJURY; AXON REGENERATION; PTEN/MTOR PATHWAY; ADULT ZEBRAFISH; C-ELEGANS; EXPRESSION; ACTIVATION;
D O I
10.1007/s10072-014-1940-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Spinal cord injury (SCI) is medically and socioeconomically debilitating, and effective treatments are lacking. The elucidation of the pathophysiological mechanisms underlying SCI is essential for developing effective treatments for SCI. MicroRNAs (miRNAs) are small non-coding RNA molecules (18-24 nucleotides long) that regulate gene expression by interacting with specific target sequences. Recent studies suggest that miRNAs can act as post-transcriptional regulators to inhibit mRNA translation. Bioinformatic analyses indicate that the altered expression of miRNAs has an effect on critical processes of SCI physiopathology, including astrogliosis, oxidative stress, inflammation, apoptosis, and neuroplasticity. Therefore, the study of miRNAs may provide new insights into the molecular mechanisms of SCI. Current studies have also provided potential therapeutic clinical applications that involve targeting mRNAs to treat SCI. This review summarizes the biogenesis and function of miRNAs and the roles of miRNAs in SCI. We also discuss the potential therapeutic applications of miRNA-based interventions for SCI.
引用
收藏
页码:1663 / 1671
页数:9
相关论文
共 87 条
[1]   Mammalian Target of Rapamycin (mTOR) Activation Increases Axonal Growth Capacity of Injured Peripheral Nerves [J].
Abe, Namiko ;
Borson, Steven H. ;
Gambello, Michael J. ;
Wang, Fan ;
Cavalli, Valeria .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (36) :28034-28043
[2]   MicroRNAs and the resolution phase of inflammation in macrophages [J].
Alam, Muhammad M. ;
O'Neill, Luke A. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2011, 41 (09) :2482-2485
[3]   microRNAs: Tiny regulators with great potential [J].
Ambros, V .
CELL, 2001, 107 (07) :823-826
[4]  
Becker CG, 2008, RESTOR NEUROL NEUROS, V26, P71
[5]   Regulation of microRNA expression in the heart by the ATF6 branch of the ER stress response [J].
Belmont, Peter J. ;
Chen, Wenqiong J. ;
Thuerauf, Donna J. ;
Glembotski, Christopher C. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2012, 52 (05) :1176-1182
[6]   Mammalian mirtron genes [J].
Berezikov, Eugene ;
Chung, Wei-Jen ;
Willis, Jason ;
Cuppen, Edwin ;
Lai, Eric C. .
MOLECULAR CELL, 2007, 28 (02) :328-336
[7]   microRNA-21 Regulates Astrocytic Response Following Spinal Cord Injury [J].
Bhalala, Oneil G. ;
Pan, Liuliu ;
Sahni, Vibhu ;
McGuire, Tammy L. ;
Gruner, Katherine ;
Tourtellotte, Warren G. ;
Kessler, John A. .
JOURNAL OF NEUROSCIENCE, 2012, 32 (50) :17935-17947
[8]   Astrocyte Function and Role in Motor Neuron Disease: A Future Therapeutic Target? [J].
Blackburn, Daniel ;
Sargsyan, Siranush ;
Monk, Peter N. ;
Shaw, Pamela J. .
GLIA, 2009, 57 (12) :1251-1264
[9]   MicroRNA-21 protects neurons from ischemic death [J].
Buller, Ben ;
Liu, Xianshuang ;
Wang, Xinli ;
Zhang, Rui L. ;
Zhang, Li ;
Hozeska-Solgot, Ann ;
Chopp, Michael ;
Zhang, Zheng G. .
FEBS JOURNAL, 2010, 277 (20) :4299-4307
[10]   PTEN Level in Tumor Suppression: How Much Is Too Little? [J].
Carracedo, Arkaitz ;
Alimonti, Andrea ;
Pandolfi, Pier Paolo .
CANCER RESEARCH, 2011, 71 (03) :629-633