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Cell labeling for magnetic resonance imaging with the T1 agent manganese chloride.
https://repo.qst.go.jp/records/44710
https://repo.qst.go.jp/records/44710cf8b9f5b-481e-49e3-9bf6-f182d532cf5e
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2006-11-20 | |||||
タイトル | ||||||
タイトル | Cell labeling for magnetic resonance imaging with the T1 agent manganese chloride. | |||||
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_6501 | |||||
資源タイプ | journal article | |||||
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 |
Aoki, Ichio
× Aoki, Ichio× et.al× 青木 伊知男 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | There is growing interest in using MRI to track cellular migration. To date, most work in this area has been performed using ultra-small particles of iron oxide. Immune cells are difficult to label with iron oxide particles. The ability of adoptively infused tumor specific T cells and N cells to traffic to the tumor microenvironment may be a critical determinant of their therapeutic efficacy.We tested the hypothesis that lymphocytes and B cells would label with MnCl2 to a level that would allow their detection by T1-weighted MRI. Significant signal enhancement was observed in human lymphocytes after a 1 h incubation with 0.05_1.0mM MnCl2. A flow cytometry-based evaluation using propidium iodide and Annexin V staining showed that lymphocytes did not undergo apoptosis or necrosis immediately after and 24 h following a 1 h incubation with up to 1.0mM MnCl2. Importantly, NK cells and cytotoxic T cells maintained their in vitro killing capacity after being incubated with up to 0.5mM MnCl2. This is the first report to describe the use of MnCl2 to label lymphocytes. Our data suggests MnCl2 might be an alternative to iron oxide cell labeling for MRI-based cell migrationstudies. | |||||
書誌情報 |
NMR in Biomedicine 巻 19, 号 1, p. 50-59, 発行日 2006 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0952-3480 |