Rutanen Juha, Rissanen Tuomas T, Markkanen Johanna E, Gruchala Marcin, Silvennoinen Päivi, Kivelä Antti, Hedman Antti, Hedman Marja, Heikura Tommi, Ordén Maija-Riitta, Stacker Steven A, Achen Marc G, Hartikainen Juha, Ylä-Herttuala Seppo
Department of Molecular Medicine, A.I. Virtanen Institute, Kuopio University, Finland.
Circulation. 2004 Mar 2;109(8):1029-35. doi: 10.1161/01.CIR.0000115519.03688.A2. Epub 2004 Feb 16.
It is unclear what is the most efficient vector and growth factor for induction of therapeutic vascular growth in the heart. Furthermore, the histological nature of angiogenesis and potential side effects caused by different vascular endothelial growth factors (VEGFs) in myocardium have not been documented.
Adenoviruses (Ad) at 2 doses (2x10(11) and 2x10(12) viral particles) or naked plasmids (1 mg) encoding LacZ control, VEGF-A165, or the mature, soluble form of VEGF-D (VEGF-D(DeltaNDeltaC)) were injected intramyocardially with the NOGA catheter system into domestic pigs. AdVEGF-D(DeltaNDeltaC) gene transfer (GT) induced a dose-dependent myocardial protein production, as measured by ELISA, resulting in an efficient angiogenic effect 6 days after the injections. Also, AdVEGF-A165 produced high gene transfer efficacy, as demonstrated with immunohistochemistry, leading to prominent angiogenesis effects. Despite the catheter-mediated approach, angiogenesis induced by both AdVEGFs was transmural, with maximal effects in the epicardium. Histologically, strongly enlarged alpha-smooth muscle actin-positive microvessels involving abundant cell proliferation were found in the transduced regions, whereas microvessel density did not change. Myocardial contrast echocardiography and microspheres showed marked increases in perfusion in the transduced areas. VEGF-D(DeltaNDeltaC) but not matrix-bound VEGF-A165 was detected in plasma after adenoviral GT. A modified Miles assay demonstrated myocardial edema resulting in pericardial effusion with the higher AdVEGF doses. All effects returned to baseline by 3 weeks. Naked plasmid-mediated GT did not induce detectable protein production or vascular effects.
Like AdVEGF-A165, AdVEGF-D(DeltaNDeltaC) GT using the NOGA system produces efficient transmural angiogenesis and increases myocardial perfusion. AdVEGF-D(DeltaNDeltaC) could be useful for the induction of therapeutic vascular growth in the heart.
目前尚不清楚在心脏中诱导治疗性血管生长的最有效载体和生长因子是什么。此外,心肌中血管生成的组织学性质以及不同血管内皮生长因子(VEGF)引起的潜在副作用尚未见报道。
采用NOGA导管系统将2种剂量(2×10¹¹和2×10¹²病毒颗粒)的腺病毒(Ad)或编码LacZ对照、VEGF-A165或成熟可溶性形式VEGF-D(VEGF-D(ΔNΔC))的裸质粒(1mg)经心肌内注射到家猪体内。通过酶联免疫吸附测定法(ELISA)检测,AdVEGF-D(ΔNΔC)基因转移(GT)诱导了剂量依赖性的心肌蛋白产生,注射后6天产生了有效的血管生成效应。此外,免疫组织化学显示AdVEGF-A165具有高基因转移效率,导致显著的血管生成效应。尽管采用了导管介导的方法,但两种AdVEGF诱导的血管生成都是透壁性的,在心外膜中效果最为显著。组织学上,在转导区域发现α-平滑肌肌动蛋白阳性微血管显著增大,伴有大量细胞增殖,而微血管密度未改变。心肌对比超声心动图和微球显示转导区域的灌注显著增加。腺病毒基因转移后,血浆中检测到VEGF-D(ΔNΔC),但未检测到与基质结合的VEGF-A165。改良的迈尔斯试验表明,较高剂量的AdVEGF会导致心肌水肿,进而引起心包积液。所有效应在3周时恢复到基线水平。裸质粒介导的基因转移未诱导可检测到的蛋白产生或血管效应。
与AdVEGF-A165一样,使用NOGA系统的AdVEGF-D(ΔNΔC)基因转移可产生有效的透壁血管生成并增加心肌灌注。AdVEGF-D(ΔNΔC)可能有助于诱导心脏的治疗性血管生长。