SUMOylation in brain ischemia: Patterns, targets, and translational implications

被引:49
作者
Bernstock, Joshua D. [1 ,2 ]
Yang, Wei [3 ]
Ye, Daniel G. [1 ]
Shen, Yuntian [3 ]
Pluchino, Stefano [2 ]
Lee, Yang-Ja [1 ]
Hallenbeck, John M. [1 ]
Paschen, Wulf [3 ,4 ]
机构
[1] NINDS, Stroke Branch, NIH, Bldg 10 Rm 5B06,MSC 1401,10 Ctr Dr, Bethesda, MD 20892 USA
[2] Univ Cambridge, Div Stem Cell Neurobiol, Dept Clin Neurosci, Wellcome Trust,MRC,Stem Cell Inst, Cambridge, England
[3] Duke Univ, Med Ctr, Dept Anesthesiol, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Neurobiol, Durham, NC 27710 USA
关键词
Brain ischemia; cell-therapy; drug repurposing; hypothermia; neuroprotection; stroke; SUMOylation; TRANSIENT FOREBRAIN ISCHEMIA; INHIBITS PROTEIN SUMOYLATION; STEM-CELL TRANSPLANTATION; FOCAL CEREBRAL-ISCHEMIA; SUMO PROTEASES; MODIFIER CONJUGATION; GLUCOSE DEPRIVATION; MOUSE-BRAIN; AGED MICE; LIFE-SPAN;
D O I
10.1177/0271678X17742260
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Post-translational protein modification by small ubiquitin-like modifier (SUMO) regulates a myriad of homeostatic and stress responses. The SUMOylation pathway has been extensively studied in brain ischemia. Convincing evidence is now at hand to support the notion that a major increase in levels of SUMOylated proteins is capable of inducing tolerance to ischemic stress. Therefore, the SUMOylation pathway has emerged as a promising therapeutic target for neuroprotection in the face of brain ischemia. Despite this, it is prudent to acknowledge that there are many key questions still to be addressed in brain ischemia related to SUMOylation. Accordingly, herein, we provide a critical review of literature within the field to summarize current knowledge and in so doing highlight pertinent translational implications of the SUMOylation pathway in brain ischemia.
引用
收藏
页码:5 / 16
页数:12
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