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Immunohistochemical analysis of transporters related to clearance of amyloid-β peptides through blood-cerebrospinal fluid barrier in human brain
https://kagawa-u.repo.nii.ac.jp/records/394
https://kagawa-u.repo.nii.ac.jp/records/3947a10f274-89e8-4b90-a795-a4ca6d61862e
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Item type | 学位論文 / Thesis or Dissertation(1) | |||||||||||
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公開日 | 2019-07-22 | |||||||||||
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言語 | en | |||||||||||
タイトル | Immunohistochemical analysis of transporters related to clearance of amyloid-β peptides through blood-cerebrospinal fluid barrier in human brain | |||||||||||
言語 | ||||||||||||
言語 | eng | |||||||||||
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資源タイプ識別子 | http://purl.org/coar/resource_type/c_db06 | |||||||||||
資源タイプ | doctoral thesis | |||||||||||
著者 |
松本, 晃一
× 松本, 晃一
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抄録 | ||||||||||||
内容記述タイプ | Abstract | |||||||||||
内容記述 | Abstract A large number of previous reports have focused on the transport of amyloid-β peptides through cerebral endothelial cells via the blood–brain barrier, while fewer reports have mentioned the transport through the choroid plexus epithelium via the blood–cerebrospinal fluid barrier. Concrete roles of these two pathways remain to be clarified. In this study, we immunohistochemically examined the expression of transporters/receptors that are supposed to be related to the clearance of amyloid-β peptides in the choroid plexus epithelium, the ventricular ependymal cells and the brain microvessels, using seven autopsied human brains. In the choroid plexus epithelium, immunoreactivity for low-density lipoprotein receptor (LDLR), LDLR-related protein 1 (LRP1), LRP2, formylpeptide receptor-like 1 (FPRL1), ATP-binding cassette (ABC) transporter-A1 (ABCA1), ABCC1 and ABCG4 was seen in 7 of 7 brains, while that for ABCB1, ABCG2, RAGE and CD36 was seen in 0–2 brains. In the ventricular ependymal cells, immunoreactivity for CD36, LDLR, LRP1, LRP2, FPRL1, ABCA1, ABCC1 and ABCG4 was seen in 6–7 brains, while that for ABCB1, ABCG2 and RAGE was seen in 0–1 brain. Immunoreactivity for insulin-degrading enzyme (IDE) was seen in three and four brains in the choroid plexus epithelium and the ventricular ependymal cells, respectively. In addition, immunoreactivity for LDLR, ABCB1 and ABCG2 was seen in over 40 % of the microvessels (all seven brains), and that for FPRL1, ABCA1, ABCC1 and RAGE was seen in over 5 % of the microvessels (4–6 brains), while that for CD36, IDE, LRP1, LRP2 and ABCG4 was seen in less than 5 % of the microvessels (0–2 brains). These findings may suggest that these multiple transporters/receptors and IDE expressed on the choroid plexus epithelium, ventricular ependymal cells and brain microvessels complementarily or cooperatively contribute to the clearance of amyloid-β peptides from the brain. |
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言語 | en | |||||||||||
学位名 | ||||||||||||
言語 | ja | |||||||||||
学位名 | 博士(医学) | |||||||||||
学位授与機関 | ||||||||||||
識別子Scheme | kakenhi | |||||||||||
識別子 | 16201 | |||||||||||
言語 | ja | |||||||||||
機関名 | 香川大学 | |||||||||||
言語 | en | |||||||||||
機関名 | Kagawa University | |||||||||||
学位授与年月日 | ||||||||||||
学位授与年月日 | 2016-02-17 | |||||||||||
学位授与番号 | ||||||||||||
学位授与番号 | 乙第274号 | |||||||||||
権利 | ||||||||||||
言語 | en | |||||||||||
権利情報 | Copyright © 2015, Springer-Verlag Berlin Heidelberg | |||||||||||
PubMed番号 | ||||||||||||
識別子タイプ | PMID | |||||||||||
関連識別子 | 26449856 | |||||||||||
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関連タイプ | isVersionOf | |||||||||||
識別子タイプ | DOI | |||||||||||
関連識別子 | https://doi.org/10.1007/s00418-015-1366-7 | |||||||||||
著者版フラグ | ||||||||||||
出版タイプ | NA | |||||||||||
出版タイプResource | http://purl.org/coar/version/c_be7fb7dd8ff6fe43 | |||||||||||
キーワード | ||||||||||||
言語 | en | |||||||||||
主題Scheme | Other | |||||||||||
主題 | Amyloid-β | |||||||||||
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言語 | en | |||||||||||
主題Scheme | Other | |||||||||||
主題 | Choroid plexus | |||||||||||
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言語 | en | |||||||||||
主題Scheme | Other | |||||||||||
主題 | Ependymal cell | |||||||||||
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言語 | en | |||||||||||
主題Scheme | Other | |||||||||||
主題 | Transporter | |||||||||||
キーワード | ||||||||||||
言語 | en | |||||||||||
主題Scheme | Other | |||||||||||
KEID | ||||||||||||
28758 |