Piersanti Stefania, Burla Romina, Licursi Valerio, Brito Catarina, La Torre Mattia, Alves Paula M, Simao Daniel, Mottini Carla, Salinas Sara, Negri Rodolfo, Tagliafico Enrico, Kremer Eric J, Saggio Isabella
Department of Biology and Biotechnology "C. Darwin", Sapienza University of Rome, Rome, Italy.
Department of Biology and Biotechnology "C. Darwin", Sapienza University of Rome, Rome, Italy; Pasteur Institute, Cenci Bolognetti Foundation, Rome, Italy.
PLoS One. 2015 Jul 24;10(7):e0133607. doi: 10.1371/journal.pone.0133607. eCollection 2015.
Brain gene transfer using viral vectors will likely become a therapeutic option for several disorders. Helper-dependent (HD) canine adenovirus type 2 vectors (CAV-2) are well suited for this goal. These vectors are poorly immunogenic, efficiently transduce neurons, are retrogradely transported to afferent structures in the brain and lead to long-term transgene expression. CAV-2 vectors are being exploited to unravel behavior, cognition, neural networks, axonal transport and therapy for orphan diseases. With the goal of better understanding and characterizing HD-CAV-2 for brain therapy, we analyzed the transcriptomic modulation induced by HD-CAV-2 in human differentiated neurospheres derived from midbrain progenitors. This 3D model system mimics several aspects of the dynamic nature of human brain. We found that differentiated neurospheres are readily transduced by HD-CAV-2 and that transduction generates two main transcriptional responses: a DNA damage response and alteration of centromeric and microtubule probes. Future investigations on the biochemistry of processes highlighted by probe modulations will help defining the implication of HD-CAV-2 and CAR receptor binding in enchaining these functional pathways. We suggest here that the modulation of DNA damage genes is related to viral DNA, while the alteration of centromeric and microtubule probes is possibly enchained by the interaction of the HD-CAV-2 fibre with CAR.
使用病毒载体进行脑基因转移可能会成为多种疾病的一种治疗选择。依赖辅助病毒的2型犬腺病毒载体(CAV-2)非常适合这一目标。这些载体免疫原性低,能有效转导神经元,可逆行运输至脑内的传入结构,并能实现转基因的长期表达。CAV-2载体正被用于揭示行为、认知、神经网络、轴突运输以及罕见病的治疗方法。为了更好地理解和表征用于脑治疗的HD-CAV-2,我们分析了HD-CAV-2在源自中脑祖细胞的人类分化神经球中诱导的转录组调控。这个三维模型系统模拟了人类大脑动态特性的几个方面。我们发现分化的神经球很容易被HD-CAV-2转导,并且转导产生两种主要的转录反应:DNA损伤反应以及着丝粒和微管探针的改变。未来对探针调控所突出的过程的生物化学研究,将有助于明确HD-CAV-2和柯萨奇病毒和腺病毒受体(CAR)结合在连接这些功能途径中的作用。我们在此提出,DNA损伤基因的调控与病毒DNA有关,而着丝粒和微管探针的改变可能是由HD-CAV-2纤维与CAR的相互作用所引发的。