Gene transfer to the vascular system: Novel translational perspectives for vascular diseases

被引:8
作者
Remes, A. [1 ,2 ,3 ]
Basha, D. I. [1 ,2 ,3 ]
Frey, N. [1 ,2 ,3 ]
Wagner, A. H. [4 ]
Mueller, O. J. [1 ,2 ,3 ]
机构
[1] Univ Kiel, Dept Internal Med 3, Partner Site Hamburg Kiel Lubeck, Kiel, Germany
[2] Univ Hosp Schleswig Holstein, Partner Site Hamburg Kiel Lubeck, Kiel, Germany
[3] German Ctr Cardiovasc Res, Partner Site Hamburg Kiel Lubeck, Berlin, Germany
[4] Heidelberg Univ, Dept Cardiovasc Physiol, Neuenheimer Feld 326, D-69120 Heidelberg, Germany
基金
欧盟地平线“2020”;
关键词
Gene therapy; Vectors; Atherosclerosis; Hyperplasia; Aneurysm; Angiogenesis; SMOOTH-MUSCLE-CELLS; ABDOMINAL AORTIC-ANEURYSM; ADENOASSOCIATED VIRUS TYPE-2; IN-STENT RESTENOSIS; INHIBITS NEOINTIMAL FORMATION; NORMAL RABBIT ARTERIES; NITRIC-OXIDE SYNTHASE; TRANSGENE EXPRESSION; ALLOGRAFT VASCULOPATHY; TISSUE INHIBITOR;
D O I
10.1016/j.bcp.2020.114265
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although vessels are directly exposed to the bloodstream, vascular gene transfer is rarely used as a tool for preclinical studies for several reasons: (i) viral and non-viral vectors show a low transduction efficiency in the vascular system; (ii) classical vascular gene therapy approaches such as treatment of peripheral or cardiac ischemia are focusing on non-vascular target cells; and (iii) vascular diseases are rarely monogenetic, thus gene replacement approaches are uncommon. Here, we provide an overview of recent approaches in developing novel vectors and modes of application for improved transduction efficiency of large and small vessels. Increased availability of such tools for vascular gene transfer has already facilitated preclinical studies addressing a broad variety of vascular diseases like transplant vasculopathy, atherosclerosis, and hereditary aortic diseases such as Marfan syndrome.
引用
收藏
页数:8
相关论文
共 118 条
[1]  
Alfonso Fernando, 2009, EuroIntervention, V5 Suppl D, pD70
[2]   High-dose AAV gene therapy deaths [J].
不详 .
NATURE BIOTECHNOLOGY, 2020, 38 (08) :910-910
[3]   A novel combination of promoter and enhancers increases transgene expression in vascular smooth muscle cells in vitro and coronary arteries in vivo after adenovirus-mediated gene transfer [J].
Appleby, CE ;
Kingston, PA ;
David, A ;
Gerdes, CA ;
Umaña, P ;
Castro, MG ;
Lowenstein, PR ;
Heagerty, AM .
GENE THERAPY, 2003, 10 (18) :1616-1622
[4]   Inhibition of graft arteriosclerosis development in rat aortas following heme oxygenase-1 gene transfer [J].
Bouchet, D ;
Chauveau, C ;
Roussel, JC ;
Mathieu, P ;
Braudeau, C ;
Tesson, L ;
Soulillou, JP ;
Iyer, S ;
Buelow, R ;
Anegon, I .
TRANSPLANT IMMUNOLOGY, 2002, 9 (2-4) :235-238
[5]   Phase 1 Gene Therapy for Duchenne Muscular Dystrophy Using a Translational Optimized AAV Vector [J].
Bowles, Dawn E. ;
McPhee, Scott W. J. ;
Li, Chengwen ;
Gray, Steven J. ;
Samulski, Jade J. ;
Camp, Angelique S. ;
Li, Juan ;
Wang, Bing ;
Monahan, Paul E. ;
Rabinowitz, Joseph E. ;
Grieger, Joshua C. ;
Govindasamy, Lakshmanan ;
Agbandje-McKenna, Mavis ;
Xiao, Xiao ;
Samulski, R. Jude .
MOLECULAR THERAPY, 2012, 20 (02) :443-455
[6]   Non-viral eNOS gene delivery and transfection with stents for the treatment of restenosis [J].
Brito, Luis A. ;
Chandrasekhar, Saradha ;
Little, Steven R. ;
Amiji, Mansoor M. .
BIOMEDICAL ENGINEERING ONLINE, 2010, 9
[7]  
Cable DG, 1999, CIRCULATION, V100, P392
[8]   CYP2J2 overexpression increases EETs and protects against angiotensin II-induced abdominal aortic aneurysm in mice [J].
Cai, Zhejun ;
Zhao, Gang ;
Yan, Jiangtao ;
Liu, Wanjun ;
Feng, Wenjing ;
Ma, Ben ;
Yang, Lei ;
Wang, Jian-an ;
Tu, Ling ;
Wang, Dao Wen .
JOURNAL OF LIPID RESEARCH, 2013, 54 (05) :1448-1456
[9]   Acute host-mediated endothelial injury after adenoviral gene transfer in normal rabbit arteries - Impact on transgene expression and endothelial function [J].
Channon, KM ;
Qian, HS ;
Youngblood, SA ;
Olmez, E ;
Shetty, GA ;
Neplioueva, V ;
Blazing, MA ;
George, SE .
CIRCULATION RESEARCH, 1998, 82 (12) :1253-1262
[10]   Recombinant adeno-associated virus serotype 9 in a mouse model of atherosclerosis: Determination of the optimal expression time in vivo [J].
Chen, Qingjie ;
Zhai, Hui ;
Li, Xiaomei ;
Ma, Yitong ;
Chen, Bangdang ;
Liu, Fen ;
Lai, Hongmei ;
Xie, Jia ;
He, Chunhui ;
Luo, Junyi ;
Gao, Jing ;
Yang, Yining .
MOLECULAR MEDICINE REPORTS, 2017, 15 (04) :2090-2096