Chang Gwendolen Y, Cao Feng, Krishnan Manickam, Huang Mei, Li Zongjin, Xie Xiaoyan, Sheikh Ahmad Y, Hoyt Grant, Robbins Robert C, Hsiai Tzung, Schneider Michael D, Wu Joseph C
The Molecular Imaging Program at Stanford (MIPS) and Department of Radiology, Stanford University, Palo Alto, CA, USA.
J Mol Cell Cardiol. 2007 Jul;43(1):18-26. doi: 10.1016/j.yjmcc.2007.03.809. Epub 2007 Mar 24.
The Cre-loxP system has been routinely used for conditional activation and deletion of gene expression. However, the spatiotemporal manner of these events in the heart has not yet been defined by in vivo imaging. Adenovirus (1 x 10(9 )pfu) carrying the silent positron emission tomography (PET) reporter gene, herpes simplex virus type 1 thymidine kinase (HSV1-tk), was injected into the left ventricular wall of male transgenic mice (n=15) or FVB controls (n=8). Transgenic mice expressed Cre recombinase driven by a cardiac-specific alpha-myosin heavy chain (alpha-MHC) promoter. Following injection of the 9-[4-fluoro-3-(hydroxymethyl)butyl]guanine ([18F]-FHBG; 137+/-25 microCi) reporter probe, microPET imaging was used to assess the expression of HSV1-tk reporter gene in the myocardium. Two days following adenoviral injection, cardiac HSV1-tk gene activation resulted in tracer uptake of 3.20+/-0.51% ID/g for alpha-MHC-Cre and 0.05+/-0.02%ID/g for control mice (P<0.01). The in vivo results were confirmed by RT-PCR and Western blot analysis. Similar transfections were evaluated in both cardiac-specific and non-cardiac-specific cell lines. Enzyme activity showed a robust correlation (r2=0.82) between in vivo molecular imaging technique and traditional in vitro enzyme assays. With further development and validation, PET imaging will likely play an important role in the noninvasive, repetitive, and quantitative measurement of conditional gene activation in the future.
Cre-loxP系统已被常规用于基因表达的条件性激活和缺失。然而,心脏中这些事件的时空方式尚未通过体内成像来定义。将携带沉默正电子发射断层扫描(PET)报告基因单纯疱疹病毒1型胸苷激酶(HSV1-tk)的腺病毒(1×10⁹ pfu)注射到雄性转基因小鼠(n = 15)或FVB对照小鼠(n = 8)的左心室壁。转基因小鼠表达由心脏特异性α-肌球蛋白重链(α-MHC)启动子驱动的Cre重组酶。注射9-[4-氟-3-(羟甲基)丁基]鸟嘌呤([¹⁸F]-FHBG;137±25 μCi)报告探针后,使用微型PET成像评估心肌中HSV1-tk报告基因 的表达。腺病毒注射两天后,心脏HSV1-tk基因激活导致α-MHC-Cre的示踪剂摄取为3.20±0.51% ID/g,对照小鼠为0.05±0.02% ID/g(P<0.01)。体内结果通过RT-PCR和蛋白质印迹分析得到证实。在心脏特异性和非心脏特异性细胞系中评估了类似的转染。酶活性显示体内分子成像技术与传统体外酶测定之间存在强相关性(r² = 0.82)。随着进一步的发展和验证,PET成像未来可能在条件性基因激活的无创、重复和定量测量中发挥重要作用。