Cartilage Restoration Center, Department of Orthopaedic Surgery, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Osteoarthritis Cartilage. 2011 Aug;19(8):1058-65. doi: 10.1016/j.joca.2011.04.009. Epub 2011 Apr 28.
To test the hypothesis that in vivo transgene expression mediated by single intra-articular injection of adeno-associated virus serotype 2 (AAV2) persists within intra-articular tissues 1 year post-injection and can be externally controlled using an AAV2-based tetracycline-inducible gene regulation system containing the tetracycline response element (TRE) promoter.
Sprague Dawley rats received intra-articular injections of AAV2-cytomegalovirus (CMV)-enhanced green fluorescent protein (GFP) and AAV2-CMV-luciferase (Luc) into their right and left knees, respectively. Luciferase expression was evaluated over 1 year using bioluminescence imaging. After sacrifice, tissues were analyzed for GFP+ cells by fluorescent microscopy. To study external control of intra-articular AAV-transgene expression, another set of rats was co-injected with AAV2-TRE-Luc and AAV2-CMV-reverse-tetracycline-controlled transactivator (rtTA) into the right knees, and AAV2-CMV-Luc and AAV2-CMV-rtTA into the left knees. Rats received oral doxycycline (Dox), an analog of tetracycline, for 7 days. Luciferase expression was assessed by bioluminescence imaging.
Luciferase expression was localized to the injected joint and persisted throughout the 1-year study period. Abundant GFP+ cells were observed within intra-articular soft tissues. Transgene expression in AAV2-TRE-Luc injected joints was upregulated by oral administration of Dox, and downregulated following its removal, at 14 days and 13 months post-AAV injection.
This longitudinal in vivo study shows that sustained and stable AAV-mediated intra-articular transgene expression can be achieved through a single intra-articular injection and can be controlled using a tetracycline-controlled inducible AAV system in a normal rat knee model. Highly regulatable long-term intra-articular transgene expression is of potential clinical utility for development of treatment strategies for chronic intra-articular disease processes such as inflammatory and degenerative arthritis.
通过单次关节内注射腺相关病毒血清型 2(AAV2),检测活体转基因表达在关节内组织中的持续时间,该转基因表达可通过基于 AAV2 的四环素诱导基因调控系统进行外部控制,该系统包含四环素反应元件(TRE)启动子。
Sprague Dawley 大鼠分别在其右膝和左膝接受 AAV2-巨细胞病毒(CMV)-增强型绿色荧光蛋白(GFP)和 AAV2-CMV-荧光素酶(Luc)的关节内注射。通过生物发光成像在 1 年内评估荧光素酶表达。处死动物后,通过荧光显微镜分析 GFP+细胞。为了研究关节内 AAV-转基因表达的外部控制,另一组大鼠右膝共注射 AAV2-TRE-Luc 和 AAV2-CMV-反向四环素调控转录激活剂(rtTA),左膝共注射 AAV2-CMV-Luc 和 AAV2-CMV-rtTA。大鼠接受 7 天的口服强力霉素(Dox),一种四环素类似物。通过生物发光成像评估荧光素酶表达。
荧光素酶表达定位于注射关节,在 1 年研究期间持续存在。在关节内软组织中观察到大量 GFP+细胞。在 AAV2-TRE-Luc 注射关节中,通过口服给予强力霉素可上调转基因表达,在 AAV 注射后 14 天和 13 个月可下调。
这项纵向体内研究表明,通过单次关节内注射可实现持续和稳定的 AAV 介导的关节内转基因表达,并可通过正常大鼠膝关节模型中的四环素调控诱导型 AAV 系统进行控制。高度可调控的长期关节内转基因表达具有潜在的临床应用价值,可用于开发治疗慢性关节内疾病过程(如炎症性和退行性关节炎)的治疗策略。