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In vivo Evaluation of Adenoviral Mediated FES-hERL PET Tracer-Reporter Gene System for Gene Therapy Monitoring

https://repo.qst.go.jp/records/71221
https://repo.qst.go.jp/records/71221
46ecd770-d5b4-42c2-b72a-2bf6ce15fbee
Item type 会議発表用資料 / Presentation(1)
公開日 2013-08-29
タイトル
タイトル In vivo Evaluation of Adenoviral Mediated FES-hERL PET Tracer-Reporter Gene System for Gene Therapy Monitoring
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Lohith, Talakad

× Lohith, Talakad

WEKO 700086

Lohith, Talakad

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Furukawa, Takako

× Furukawa, Takako

WEKO 700087

Furukawa, Takako

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Mori, Tetsuya

× Mori, Tetsuya

WEKO 700088

Mori, Tetsuya

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Fujibayashi, Yasuhisa

× Fujibayashi, Yasuhisa

WEKO 700089

Fujibayashi, Yasuhisa

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et.al

× et.al

WEKO 700090

et.al

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古川 高子

× 古川 高子

WEKO 700091

en 古川 高子

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藤林 康久

× 藤林 康久

WEKO 700092

en 藤林 康久

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抄録
内容記述タイプ Abstract
内容記述 A key step in advancing gene therapy protocols is to establish an efficient monitoring system following target gene delivery. Earlier, we reported our new adenoviral mediated PET reporter gene system utilizing [18F]16alpha-fluoroestradiol (FES) as PET probe and human estrogen receptor alpha ligand binding domain (hERL) as PET reporter gene and evaluated basic cell culture and initial in vivo autoradiographic studies in mice [1]. Now, we report further cell model studies and in vivo PET imaging in rats.
An in vitro FES binding study was performed on MRC-5 (human lung fibroblasts) and Cos-7 (African green monkey kidney) cells infected with varying titers of test and control viruses or transfected with varying amounts of test plasmid. After 10 min uptake and 30 min intermittent wash, the FES accumulation was higher in both the cell lines infected with test virus than those transfected by test plasmid. The uptake also increased with rise in viral titer in contrast to decreasing uptake with increased plasmid amounts. The co-expression of hERL and a model therapeutic gene by the correspondingly infected cells confirmed the results of binding study.
The rats were injected with test and control adenoviruses into opposite hind limb adductor muscles. In vivo PET imaging in 6-days post-infected rat yielded positive accumulation of FES on the side injected with test virus. Furthermore, the correspondingly resected muscle samples were subjected to immunohistochemical staining and the expression of reporter and therapeutic genes were confirmed. Thus, we could successfully image the expression of our reporter gene hERL in vivo in a localized area of muscle tissue in rats. We hope confirmation of reporter gene expression following infection in other target areas will enable our system to be a significant addition to the existing repertoires of reporter gene system.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 Joint Molecular Imaging Conference
発表年月日
日付 2007-09-11
日付タイプ Issued
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