Endothelium-targeted gene and cell-based therapies for cardiovascular disease

被引:52
作者
Melo, LG
Gnecchi, M
Pachori, AS
Kong, DL
Wang, K
Liu, XL
Pratt, RE
Dzau, VJ
机构
[1] Queens Univ, Dept Physiol, Kingston, ON K7L 3N6, Canada
[2] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
关键词
endothelial progenitor cells; endothelial-specific expression; gene therapy; targeting; viral vectors;
D O I
10.1161/01.ATV.0000142363.15113.88
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Most common cardiovascular diseases are accompanied by endothelial dysfunction. Because of its predominant role in the pathogenesis of cardiovascular disease, the vascular endothelium is an attractive therapeutic target. The identification of promoter sequences capable of rendering endothelial-specific transgene expression together with the recent development of vectors with enhanced tropism for endothelium may offer opportunities for the design of new strategies for modulation of endothelial function. Such strategies may be useful in the treatment of chronic diseases such as hypertension, atherosclerosis, and ischemic artery disease, as well as in acute myocardial infarction and during open heart surgery for prevention of ischemia and reperfusion (I/R)-induced injury. The recent identification of putative endothelial progenitor cells in peripheral blood may allow the design of autologous cell-based strategies for neovascularization of ischemic tissues and for the repair of injured blood vessels and bioengineering of vascular prosthesis. "Proof-of-concept" for some of these strategies has been established in animal models of cardiovascular disease. However the successful translation of these novel strategies into clinical application will require further developments in vector and delivery technologies. Further characterization of the processes involved in mobilization, migration, homing, and incorporation of endothelial progenitor cells into the target tissues is necessary, and the optimal conditions for therapeutic application of these cells need to be defined and standardized.
引用
收藏
页码:1761 / 1774
页数:14
相关论文
共 169 条
[1]   HUMAN VON-WILLEBRAND-FACTOR GENE-SEQUENCES TARGET EXPRESSION TO A SUBPOPULATION OF ENDOTHELIAL-CELLS IN TRANSGENIC MICE [J].
AIRD, WC ;
JAHROUDI, N ;
WEILERGUETTLER, H ;
RAYBURN, HB ;
ROSENBERG, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (10) :4567-4571
[2]   The delivery of antisense therapeutics [J].
Akhtar, S ;
Hughes, MD ;
Khan, A ;
Bibby, M ;
Hussain, M ;
Nawaz, Q ;
Double, J ;
Sayyed, P .
ADVANCED DRUG DELIVERY REVIEWS, 2000, 44 (01) :3-21
[3]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[4]   Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228
[5]   HMG-CoA reductase inhibitors reduce senescence and increase proliferation of endothelial progenitor cells via regulation of cell cycle regulatory genes [J].
Assmus, B ;
Urbich, C ;
Aicher, A ;
Hofmann, WK ;
Haendeler, J ;
Rössig, L ;
Spyridopoulos, I ;
Zeiher, AM ;
Dimmeler, S .
CIRCULATION RESEARCH, 2003, 92 (09) :1049-1055
[6]   Retroviral-mediated transduction of endothelial cells with the lac Z gene impairs cellular proliferation in vitro and graft endothelialization in vivo [J].
Baer, RP ;
Whitehill, TE ;
Sarkar, R ;
Sarkar, M ;
Messina, LM ;
Komorowski, TA ;
Stanley, JC .
JOURNAL OF VASCULAR SURGERY, 1996, 24 (05) :892-899
[7]   In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium [J].
Bainbridge, JWB ;
Stephens, C ;
Parsley, K ;
Demaison, C ;
Halfyard, A ;
Thrasher, AJ ;
Ali, RR .
GENE THERAPY, 2001, 8 (21) :1665-1668
[8]   Administration of granulocyte colony-stimulating factor enhances endothelialization and microvessel formation in small-caliber synthetic vascular grafts [J].
Bhattacharya, V ;
Shi, Q ;
Ishida, A ;
Sauvage, LR ;
Hammond, WP ;
Wu, MHD .
JOURNAL OF VASCULAR SURGERY, 2000, 32 (01) :116-122
[9]   Transfection-free and scalable recombinant AAV vector production using HSV/AAV hybrids [J].
Booth, MJ ;
Mistry, A ;
Li, X ;
Thrasher, A ;
Coffin, RS .
GENE THERAPY, 2004, 11 (10) :829-837
[10]   Isolation of endothelial cells and their progenitor cells from human peripheral blood [J].
Boyer, M ;
Townsend, LE ;
Vogel, LM ;
Falk, J ;
Reitz-Vick, D ;
Trevor, KT ;
Villalba, M ;
Bendick, PJ ;
Glover, JL .
JOURNAL OF VASCULAR SURGERY, 2000, 31 (01) :181-189