AdVEGF165 gene transfer increases survival in overdimensioned skin flaps

被引:42
作者
Giunta, RE
Holzbach, T
Taskov, C
Holm, PS
Konerding, MA
Schams, D
Biemer, E
Gänsbacher, B
机构
[1] Tech Univ Munich, Rechts Isar Hosp, Dept Plast & Reconstruct Surg, D-81675 Munich, Germany
[2] Tech Univ Munich, Inst Expt Oncol & Therapy Res, D-8000 Munich, Germany
[3] Univ Technol Weihenstephan, Dept Physiol, Zent Inst Ernahrungs & Lebensmittelforsch, Weihenstephan, Germany
[4] Johannes Gutenberg Univ Mainz, Inst Anat, D-6500 Mainz, Germany
关键词
VEGF; gene therapy; skin flap; angiogenesis; adenovirus; gene transfer;
D O I
10.1002/jgm.675
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
Background Vascular endothelial growth factor (VEGF) is a key regulator of angiogenesis. VEGF A also plays an important role in wound healing of the skin by promoting angiogenesis and by stimulating blood vessel growth. Therefore we tested the hypothesis that flap survival could be increased by the preoperative injection of AdVEGF(165). Methods We studied the effect of AdVEGF(165) in an overdimensioned ischemic random-pattem-flap model in the rat (n = 50) with a length-to-width ratio of 4: 1. VEGF cDNA was administered in two concentrations of 5 x 10(8) plaque-forming units (pfU) and 1 x 10(9) pfU using a recombinant adenoviral vector. Recombinant virus was injected subdermally 7, 3 or 0 days prior to flap harvest for the lower concentration and 7 days prior for the higher concentration. Flap survival and necrosis were observed at day 7, the day the animals were sacrificed. Results Adenoviral gene transfer with VEGF(165) 3 and 7 days before flap harvest showed a significantly increased flap survival of 50% together with a significantly reduced necrosis (p < 0.01). Injection using a titer of 1 x 10(9) pfU 7 days prior to surgery increased flap survival even more, though failing to reach statistical significance compared to the lower concentration. VEGF protein concentration in the injected skin was significantly higher than in controls (p < 0.01). Flap perfusion was increased as well, demonstrated by indocyanine green (ICG) fluoroscopy (p < 0.001). Conclusions Our results confirm the important role of VEGF(165) on angiogenesis in ischemic flaps. Indeed by injecting VEGF(165) at 3 to 7 days preoperatively in a concentration of 1 x 10(9) pfU our data show that length-to-width ratio for random-pattern-flaps could be increased from 2: 1 to 3: 1 and therefore may allow a wider range of applications of this simple flap technique. Copyright (c) 2004 John Wiley & Sons, Ltd.
引用
收藏
页码:297 / 306
页数:10
相关论文
共 33 条
[1]
Vasodilator effect and mechanism of action of vascular endothelial growth factor in skin vasculature [J].
Ashrafpour, H ;
Huang, N ;
Neligan, PC ;
Forrest, CR ;
Addison, PD ;
Moses, MA ;
Levine, RH ;
Pang, CY .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2004, 286 (03) :H946-H954
[2]
Expression and tissue concentration of vascular endothelial growth factor, its receptors, and localization in the bovine corpus luteum during estrous cycle and pregnancy [J].
Berisha, B ;
Schams, D ;
Kosmann, M ;
Amselgruber, W ;
Einspanier, R .
BIOLOGY OF REPRODUCTION, 2000, 63 (04) :1106-1114
[3]
Chalkley HW, 1943, J NATL CANCER I, V4, P47
[4]
Cui Lei, 2003, Chin J Traumatol, V6, P199
[5]
The biology of VEGF and its receptors [J].
Ferrara, N ;
Gerber, HP ;
LeCouter, J .
NATURE MEDICINE, 2003, 9 (06) :669-676
[6]
Effect of transfection time on the survival of epigastric skin flaps pretreated with adenovirus encoding the VEGF gene [J].
Gurunluoglu, R ;
Ozer, K ;
Skugor, B ;
Lubiatowski, P ;
Carnevale, K ;
Siemionow, M .
ANNALS OF PLASTIC SURGERY, 2002, 49 (02) :161-169
[7]
Safety and feasibility of catheter-based local intracoronary vascular endothelial growth factor gene transfer in the prevention of postangioplasty and in-stent restenosis and in the treatment of chronic myocardial ischemia -: Phase II results of the Kuopio Angiogenesis Trial (KAT) [J].
Hedman, M ;
Hartikainen, J ;
Syvänne, M ;
Stjernvall, J ;
Hedman, A ;
Kivelä, A ;
Vanninen, E ;
Mussalo, H ;
Kauppila, E ;
Simula, S ;
Närvänen, O ;
Rantala, A ;
Peuhkurinen, K ;
Nieminen, MS ;
Laakso, M ;
Ylä-Herttuala, S .
CIRCULATION, 2003, 107 (21) :2677-2683
[8]
Multidrug-resistant cancer cells facilitate E1-independent adenoviral replication:: Impact for cancer gene therapy [J].
Holm, PS ;
Lage, H ;
Bergmann, S ;
Jürchott, K ;
Glockzin, G ;
Bernshausen, A ;
Mantwill, K ;
Ladhoff, A ;
Wichert, A ;
Mymryk, JS ;
Ritter, T ;
Dietel, M ;
Gänsbacher, B ;
Royer, HD .
CANCER RESEARCH, 2004, 64 (01) :322-328
[9]
[10]
Myocardial gene therapy [J].
Isner, JM .
NATURE, 2002, 415 (6868) :234-239