Promoting brain remodeling to aid in stroke recovery

被引:72
|
作者
Zhang, Zheng Gang [1 ]
Chopp, Michael [1 ,2 ]
机构
[1] Henry Ford Hosp, Dept Neurol, Detroit, MI 48202 USA
[2] Oakland Univ, Dept Phys, Rochester, MI 48063 USA
基金
美国国家卫生研究院;
关键词
neurorestorative therapy; stroke recovery; miRNAs; exosomes; MESENCHYMAL STROMAL CELLS; WHITE-MATTER; FUNCTIONAL RECOVERY; OLIGODENDROCYTE DIFFERENTIATION; NEUROVASCULAR PLASTICITY; AXONAL OUTGROWTH; SONIC HEDGEHOG; LINEAGE CELLS; PTEN; MICRORNAS;
D O I
10.1016/j.molmed.2015.07.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endogenous brain repair after stroke involves a set of highly interactive processes, such as angiogenesis, neurogenesis, oligodendrogenesis, synaptogenesis, and axonal outgrowth, which together orchestrate neurological recovery. During the past several years, there have been advances in our understanding of miRNAs and histone deacetylases (HDACs) in brain repair processes after stroke. Emerging data indicate the important role of exosomes for intercellular communication in promoting coupled brain remodeling processes. These advances will likely have a major impact on the development of restorative therapies for ischemic brain repair, consequently leading to improvement of neurological function. In this review, we provide an update on our current understanding of cellular and molecular mechanisms of miRNAs, exosomes, and HDACs in brain restorative processes after stroke.
引用
收藏
页码:543 / 548
页数:6
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