The Need for New Biomarkers to Assist with Stroke Prevention and Prediction of Post-Stroke Therapy Based on Plasma-Derived Extracellular Vesicles

被引:12
|
作者
Driga, Mircea Popescu [1 ,2 ]
Catalin, Bogdan [2 ,3 ]
Olaru, Denisa Greta [2 ]
Slowik, Agnieszka [4 ]
Plesnila, Nikolaus [5 ]
Hermann, Dirk M. [1 ]
Popa-Wagner, Aurel [1 ,2 ]
机构
[1] Univ Duisburg Essen, Univ Hosp Essen, Dept Neurol, D-45147 Essen, Germany
[2] Univ Med & Pharm Craiova, Expt Res Ctr Normal & Pathol Aging, Craiova 200349, Romania
[3] Univ Med & Pharm Craiova, Dept Physiol, Craiova 200349, Romania
[4] Jagiellonian Univ Med Coll, Dept Neurol, Anny 12, PL-31008 Krakow, Poland
[5] Univ Munich LMU, Inst Stroke & Dementia Res ISD, Feodor Lynen Str 17, D-81377 Munich, Germany
基金
欧盟地平线“2020”;
关键词
cerebral ischemia; neurovascular unit; aging; exosomes; biomarkers; therapy; prevention; ISCHEMIC-STROKE; FUNCTIONAL RECOVERY; SUBVENTRICULAR ZONE; CEREBRAL-ISCHEMIA; BRAIN-INJURY; EXOSOMES; MICROGLIA; CELLS; THROMBECTOMY; ASTROCYTES;
D O I
10.3390/biomedicines9091226
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
The risk of having a stroke event doubles each decade after the age of 55. Therefore, it is of great interest to develop neurorestorative therapies of stroke which occurs mostly in elderly people. However, to date, patients at risk for these sequels of stroke are not duly diagnosed and treated due to the lack of reliable biomarkers. Extracellular vesicles (EVs) are lipid bilayer-delimited particles that are shed by the brain cells and are able to cross the blood-brain barrier and enter the blood stream; thus, they may be used to interrogate molecular and cellular events in the brain damaged area. In this review, we summarize the major molecular and cellular responses of astroglia and neurons to cerebral ischemia and assess their impact on post-stroke recovery and rehabilitation. In particular, we ask if EVs secreted by brain cells are responses to cerebral ischemia, and they may shed new light on the interplay between exosomes-mediated interactions between brain cells and the question of how to exploit it in order to predict the individual course of the disease and to introduce specific preventive or therapeutic strategies. Given these findings, we are left with two options: either to (i) transplant neuronal precursors into the damaged cortical area or (ii) to covert abundantly present proliferating astrocytes in the perilesional area into neurons by using recently developed genetic technologies. However, given the complexity of molecular and cellular responses to cerebral ischemia and our limited capabilities to restore brain structure and function, we are left with only one realistic aim: to invest more in prevention.
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页数:16
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