共 50 条
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
来源:
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.
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页码:11402 / 11407
页数:6
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