Department of Neurosurgery, University of Lausanne, Lausanne, Switzerland.
Mol Med. 2010 Sep-Oct;16(9-10):433-7. doi: 10.2119/molmed.2010.00035. Epub 2010 Jun 30.
Neural stem cells have been proposed as a new and promising treatment modality in various pathologies of the central nervous system, including malignant brain tumors. However, the underlying mechanism by which neural stem cells target tumor areas remains elusive. Monitoring of these cells is currently done by use of various modes of molecular imaging, such as optical imaging, magnetic resonance imaging and positron emission tomography, which is a novel technology for visualizing metabolism and signal transduction to gene expression. In this new context, the microenvironment of (malignant) brain tumors and the blood-brain barrier gains increased interest. The authors of this review give a unique overview of the current molecular-imaging techniques used in different therapeutic experimental brain tumor models in relation to neural stem cells. Such methods for molecular imaging of gene-engineered neural stem/progenitor cells are currently used to trace the location and temporal level of expression of therapeutic and endogenous genes in malignant brain tumors, closing the gap between in vitro and in vivo integrative biology of disease in neural stem cell transplantation.
神经干细胞被提议作为一种新的、有前途的治疗方法,用于治疗中枢神经系统的各种病变,包括恶性脑肿瘤。然而,神经干细胞靶向肿瘤区域的潜在机制仍不清楚。目前,这些细胞的监测是通过使用各种分子成像模式来完成的,如光学成像、磁共振成像和正电子发射断层扫描,这是一种用于可视化代谢和信号转导到基因表达的新技术。在这个新的背景下,(恶性)脑肿瘤的微环境和血脑屏障引起了更多的关注。本文的作者对目前用于不同治疗性实验性脑肿瘤模型中与神经干细胞相关的分子成像技术进行了独特的综述。目前,用于基因工程神经干细胞/祖细胞的分子成像方法被用于追踪治疗性和内源性基因在恶性脑肿瘤中的位置和时间表达水平,缩小了神经干细胞移植中疾病体外和体内整合生物学之间的差距。