Protection by neuroglobin and cell-penetrating peptide-mediated delivery in vivo: A decade of research Comment on Cai et al.: TAT-mediated delivery of neuroglobin protects against focal cerebral ischemia in mice. Exp Neurol. 2011; 227(1): 224-31

被引:18
作者
Dietz, Gunnar P. H. [1 ]
机构
[1] H Lundbeck & Co AS, Neurodegenerat 2, Dep 851, DK-2500 Copenhagen, Denmark
关键词
Hypoxia; Ischemia; Cell-penetrating peptide (CPP); Protein transduction domain (PTD); Stroke; Transactivator of transcription (Tat); Antp (antennapedia); NF-KAPPA-B; LONG-TERM NEUROPROTECTION; REGIONAL BRAIN ISCHEMIA; FUSION PROTEIN; BCL-XL; C-JUN; ISCHEMIA/REPERFUSION INJURY; EFFICIENTLY PROTECTS; OXIDATIVE STRESS; PRECURSOR CELLS;
D O I
10.1016/j.expneurol.2011.05.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Over the last decade, numerous studies have suggested that neuroglobin is able to protect against the effects of ischemia. However, such results have mostly been based on models using transgenic overexpression or viral delivery. As a therapy, new technology would need to be applied to enable delivery of high concentrations of neuroglobin shortly after the patient suffers the stroke. An approach to deliver proteins in ischemia in vivo in a timely manner is the use of cell-penetrating peptides (CPP). CPP have been used in animal models for brain diseases for about a decade as well. In a recent issue of Experimental Neurology, Cai and colleagues test the effect of CPP-coupled neuroglobin in an in vivo stroke model. They find that the fusion protein protects the brain against the effect of ischemia when applied before stroke onset. Here, a concise review of neuroglobin research and the application of CPP peptides in hypoxia and ischemia is provided. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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