转导(生物物理学)
腺相关病毒
遗传增强
赫拉
基因传递
内皮干细胞
病毒
生物
细胞
再狭窄
病毒载体
基因
细胞生物学
分子生物学
病毒学
载体(分子生物学)
医学
体外
遗传学
生物化学
内科学
重组DNA
支架
作者
Juan A. Merchan,Jarrod Dean,Federico Azpurua,Sabyasachi Sen,Yan Zhu,Ryuichi Aikawa
出处
期刊:PubMed
日期:2008-09-01
被引量:3
摘要
Vascular endothelial cells (EC) have been targeted for the treatment of pathological conditions such as atherosclerosis, hypercholesterolemia, post-angioplasty restenosis and hypertension. Non-pathogenic adeno-associated virus (AAV) has been shown as a good gene delivery tool in a variety of cell lines as well as in animal models. However, AAV has been reported to induce less endothelial cell transduction. AAV vector alone transduced HUVEC much lower than other cell lines including Hela, PAC1, and C2C12. Preincubation of AAV vector with EC membrane specific peptides markedly increased AAV transduction of HUVEC. On the contrary, those peptides did not affect AAV expression in other cell types. These EC-specific peptides may be a strategy for enhancement of AAV mediated-gene expression.
科研通智能强力驱动
Strongly Powered by AbleSci AI