VEGFA Isoforms as Pro-Angiogenic Therapeutics for Cerebrovascular Diseases

被引:16
|
作者
White, Amanda Louise [1 ,2 ]
Bix, Gregory Jaye [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Tulane Univ, Clin Neurosci Res Ctr, Dept Neurosurg, Sch Med, New Orleans, LA 70112 USA
[2] Tulane Univ, Tulane Brain Inst, New Orleans, LA 70112 USA
[3] Tulane Univ, Sch Med, New Orleans, LA 70112 USA
[4] Tulane Univ, Dept Neurol, Sch Med, New Orleans, LA 70112 USA
[5] Tulane Univ, Dept Microbiol & Immunol, Sch Med, New Orleans, LA 70112 USA
[6] Tulane Univ, Sch Publ Hlth & Trop Med, New Orleans, LA 70122 USA
关键词
VEGFA; isoforms; cerebral vasculature; angiogenic therapy; ENDOTHELIAL GROWTH-FACTOR; CORONARY-ARTERY-DISEASE; FOCAL CEREBRAL-ISCHEMIA; GENE-THERAPY; FOLLOW-UP; INTRAMYOCARDIAL INJECTION; ENHANCES ANGIOGENESIS; MYOCARDIAL-PERFUSION; LESION MODEL; BRAIN-INJURY;
D O I
10.3390/biom13040702
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
Therapeutic angiogenesis has long been considered a viable treatment for vasculature disruptions, including cerebral vasculature diseases. One widely-discussed treatment method to increase angiogenesis is vascular endothelial growth factor (VEGF) A. In animal models, treatment with VEGFA proved beneficial, resulting in increased angiogenesis, increased neuronal density, and improved outcome. However, VEGFA administration in clinical trials has thus far failed to replicate the promising results seen in animal models. The lack of beneficial effects in humans and the difficulty in medicinal translation may be due in part to administration methods and VEGFA's ability to increase vascular permeability. One solution to mitigate the side effects of VEGFA may be found in the VEGFA isoforms. VEGFA is able to produce several different isoforms through alternative splicing. Each VEGFA isoform interacts differently with both the cellular components and the VEGF receptors. Because of the different biological effects elicited, VEGFA isoforms may hold promise as a tangible potential therapeutic for cerebrovascular diseases.
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收藏
页数:17
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