Endothelial cells are activated by angiopoeitin-1 gene transfer and produce coordinated sprouting in vitro and arteriogenesis in vivo

被引:27
作者
Gluzman, Zoya
Koren, Belly
Preis, Meir
Cohen, Tzafra
Tsaba, Adili
Cosset, Francois-Loic
Shofti, Rona
Lewis, Basil S.
Virmani, Renu
Flugelman, Moshe Y.
机构
[1] Lady Davies Carmel Med Ctr, Dept Cardiovasc Med, IL-34362 Haifa, Israel
[2] Lady Davies Carmel Med Ctr, MultiGene Vasc Syst Ltd, IL-34362 Haifa, Israel
[3] Technion Israel Inst Technol, Ruth & Bruce Rappaport Sch Med, Haifa, Israel
[4] INSERM, Lab Vectorol Retrovirale & Therapie Gen, U412, F-69008 Lyon, France
[5] Armed Forces Inst Pathol, Washington, DC USA
关键词
endothelial cells; smooth muscle cells; VEGF; angiopoeitin-1; arteriogenesis;
D O I
10.1016/j.bbrc.2007.05.097
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
Rational and objectives: Activation of fully differentiated vascular cells using angiogenic genes can lead to phenotypic changes resulting in formation of new blood vessels. We tested whether Ang-1 gene transfer to endothelial cells (EC) activates these cells. Methods and results: EC and SMC were transduced using retroviral or adenoviral vectors to produce Ang-1 or vascular endothelial growth factor (VEGF). EC Tie-2 receptor was phosphorilated by autologous secretion of Ang-1. Transduced EC and SMC sprouting capacity was tested using collagen embedded spheroids assay and capacity to produce arteriogenesis was tested in a hind limb model of ischemia. EC expressing Ang-1 in the presence of SMC expressing VEGF exhibited high levels of sprouting of the two cell types. Flow and numbers of arteries were increased after transduced cells implantation in vivo. Conclusions: Autologous secretion of Ang-1 by transduced EC resulted in Tie-2 activation and in the presence of SMC expressing VEGF resulted in coordinated sprouting in vitro and increase in flow and number of arteries in vivo. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:263 / 268
页数:6
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