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Effects of endocytosis inhibitors on internalization of human IgG by Caco-2 human intestinal epithelial cells

https://hiroshima.repo.nii.ac.jp/records/2007647
https://hiroshima.repo.nii.ac.jp/records/2007647
d2fb538f-5ac1-47b9-b17d-1eaa57a91d20
名前 / ファイル ライセンス アクション
LifeSci_85_800.pdf LifeSci_85_800.pdf (530.9 KB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Effects of endocytosis inhibitors on internalization of human IgG by Caco-2 human intestinal epithelial cells
言語 en
作成者 Sato, Koya

× Sato, Koya

en Sato, Koya

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Nagai, Junya

× Nagai, Junya

en Nagai, Junya

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Mitsui, Naoko

× Mitsui, Naoko

en Mitsui, Naoko

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Yumoto, Ryoko

× Yumoto, Ryoko

en Yumoto, Ryoko

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Takano, Mikihisa

× Takano, Mikihisa

en Takano, Mikihisa

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 Copyright (c) 2009 Elsevier Inc. All rights reserved.
主題
主題Scheme Other
主題 IgG
主題
主題Scheme Other
主題 FcRn
主題
主題Scheme Other
主題 Endocytosis
主題
主題Scheme Other
主題 Caco-2 cells
主題
主題Scheme Other
主題 Intestine
主題
主題Scheme NDC
主題 490
内容記述
内容記述 Aims: The purpose of this study was to characterize the internalization mechanism of human IgG into the epithelial cells of human small intestine. employing human intestinal epithelial cell line Caco-2 as an in vitro model system. Main methods: Real-time PCR analysis and uptake studies of fluorescein isothiocyanate-labeled IgG (FITC-IgG) from human serum were performed using Caco-2 cells. Key findings: Real-time PCR analysis showed that mRNA level of the neonatal Fc receptor (FcRn) was increased during the differentiation process in Caco-2 cells. The binding of FITC-labeled human IgG to the membrane surface of Caco-2 cells increased with a decrease in pH of incubation buffer. The uptake of FITC-IgG was also stimulated at acidic pH and was time-dependent. The binding and uptake of FITC-IgG at pH 6.0 was partially, but significantly, decreased by human gamma-globulin in a concentration-dependent manner. A mixture of metabolic inhibitors (sodium azide and 2-deoxyglucose) significantly inhibited the uptake, but not the binding, of FITC-IgG. In addition, endosomal acidification inhibitors such as bafilomycin A, and chloroquine significantly increased the accumulation of FITC-IgG. Clathrin-dependent endocytosis inhibitors (phenylarsine oxide and chlorpromazine) and caveolin-dependent endocytosis inhibitors (nystatin and indomethacin) did not decrease the uptake of FITC-IgG at pH 6.0. In contrast, macropinocytosis inhibitors such as cytochalasin B and 5-(N-ethyl-N-isopropyl) amiloride significantly decreased the uptake of FITC-IgG at pH 6.0. Significance: The internalization of human IgG in human intestine might be, at least in part, due to FcRn-mediated endocytosis. which could occur by a process other than clathrin- and caveolin-dependent mechanisms.
言語 en
出版者
出版者 Pergamon
出版者
出版者 Elsevier Science Ltd
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
出版タイプ
出版タイプ AO
出版タイプResource http://purl.org/coar/version/c_b1a7d7d4d402bcce
関連情報
識別子タイプ DOI
関連識別子 10.1016/j.lfs.2009.10.012
関連情報
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1016/j.lfs.2009.10.012
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0024-3205
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA00717011
開始ページ
開始ページ 800
書誌情報 Life Sciences
Life Sciences

巻 85, 号 23-26, p. 800-807, 発行日 2009-12-16
旧ID 29237
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