Gene Manipulation Strategies to Identify Molecular Regulators of Axon Regeneration in the Central Nervous System

被引:19
作者
Ribas, Vinicius T. [1 ]
Costa, Marcos R. [2 ]
机构
[1] Univ Fed Minas Gerais, Inst Biol Sci, Dept Morphol, Lab Neurobiol, Belo Horizonte, MG, Brazil
[2] Univ Fed Rio Grande do Norte, Brain Inst, Natal, RN, Brazil
来源
FRONTIERS IN CELLULAR NEUROSCIENCE | 2017年 / 11卷
关键词
genetic manipulation; adeno-associated virus; transgenic animals; axon regeneration; central nervous system; SPINAL-CORD-INJURY; RETINAL GANGLION-CELLS; ADENOASSOCIATED VIRUS SEROTYPES; CORTICOSPINAL TRACT AXONS; IN-VIVO; VIRAL VECTORS; NEUROLOGICAL DISORDERS; TRANSGENE EXPRESSION; CONGENITAL AMAUROSIS; FUNCTIONAL RECOVERY;
D O I
10.3389/fncel.2017.00231
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Limited axon regeneration in the injured adult mammalian central nervous system (CNS) usually results in irreversible functional deficits. Both the presence of extrinsic inhibitory molecules at the injury site and the intrinsically low capacity of adult neurons to grow axons are responsible for the diminished capacity of regeneration in the adult CNS. Conversely, in the embryonic CNS, neurons show a high regenerative capacity, mostly due to the expression of genes that positively control axon growth and downregulation of genes that inhibit axon growth. A better understanding of the role of these key genes controlling pro-regenerative mechanisms is pivotal to develop strategies to promote robust axon regeneration following adult CNS injury. Genetic manipulation techniques have been widely used to investigate the role of specific genes or a combination of different genes in axon regrowth. This review summarizes a myriad of studies that used genetic manipulations to promote axon growth in the injured CNS. We also review the roles of some of these genes during CNS development and suggest possible approaches to identify new candidate genes. Finally, we critically address the main advantages and pitfalls of gene-manipulation techniques, and discuss new strategies to promote robust axon regeneration in the mature CNS.
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页数:18
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