Positron emission tomography reporter gene strategy for use in the central nervous system

被引:32
|
作者
Haywood, Tom [1 ]
Beinat, Corinne [1 ]
Gowrishankar, Gayatri [1 ]
Patel, Chirag B. [1 ,2 ]
Alam, Israt S. [1 ]
Murty, Surya [1 ]
Gambhir, Sanjiv Sam [1 ]
机构
[1] Stanford Univ, Dept Radiol, Mol Imaging Program, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
关键词
reporter gene; positron emission tomography (PET); PKM2; 18F] DASA-23; adeno-associated virus; PYRUVATE-KINASE M2; MOUSE MODEL; LIVING ANIMALS; IN-VITRO; DELIVERY; THERAPY; BRAIN; EXPRESSION; PKM2; RECEPTOR;
D O I
10.1073/pnas.1901645116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
There is a growing need for monitoring or imaging gene therapy in the central nervous system (CNS). This can be achieved with a positron emission tomography (PET) reporter gene strategy. Here we report the development of a PET reporter gene system using the PKM2 gene with its associated radiotracer [F-18] DASA-23. The PKM2 reporter gene was delivered to the brains of mice by adeno-associated virus (AAV9) via stereotactic injection. Serial PET imaging was carried out over 8 wk to assess PKM2 expression. After 8 wk, the brains were excised for further mRNA and protein analysis. PET imaging at 8 wk post-AAV delivery showed an increase in [F-18] DASA-23 brain uptake in the transduced site of mice injected with the AAV mice over all controls. We believe PKM2 shows great promise as a PET reporter gene and to date is the only example that can be used in all areas of the CNS without breaking the blood-brain barrier, to monitor gene and cell therapy.
引用
收藏
页码:11402 / 11407
页数:6
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