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Inhibition of Casein Kinase 2 Modulates XBP1-GRP78 Arm of Unfolded Protein Responses in Cultured Glial Cells

https://hiroshima.repo.nii.ac.jp/records/2007950
https://hiroshima.repo.nii.ac.jp/records/2007950
94bd69d7-b7e4-4645-aaa6-a7d68795db4a
名前 / ファイル ライセンス アクション
PLoS-One_7_e40144.pdf PLoS-One_7_e40144.pdf (2.7 MB)
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 Inhibition of Casein Kinase 2 Modulates XBP1-GRP78 Arm of Unfolded Protein Responses in Cultured Glial Cells
言語 en
作成者 Hosoi, Toru

× Hosoi, Toru

en Hosoi, Toru

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Korematsu, Kenta

× Korematsu, Kenta

en Korematsu, Kenta

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Horie, Naohiro

× Horie, Naohiro

en Horie, Naohiro

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Suezawa, Takahiro

× Suezawa, Takahiro

en Suezawa, Takahiro

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Ozawa, Koichiro

× Ozawa, Koichiro

en Ozawa, Koichiro

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Okuma, Yasunobu

× Okuma, Yasunobu

en Okuma, Yasunobu

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Nomura, Yasuyuki

× Nomura, Yasuyuki

en Nomura, Yasuyuki

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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 (c) 2012 Hosoi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
主題
主題Scheme NDC
主題 490
内容記述
内容記述 Stress signals cause abnormal proteins to accumulate in the endoplasmic reticulum (ER). Such stress is known as ER stress, which has been suggested to be involved in neurodegenerative diseases, diabetes, obesity and cancer. ER stress activates the unfolded protein response (UPR) to reduce levels of abnormal proteins by inducing the production of chaperon proteins such as GRP78, and to attenuate translation through the phosphorylation of eIF2 alpha. However, excessive stress leads to apoptosis by generating transcription factors such as CHOP. Casein kinase 2 (CK2) is a serine/threonine kinase involved in regulating neoplasia, cell survival and viral infections. In the present study, we investigated a possible linkage between CK2 and ER stress using mouse primary cultured glial cells. 4,5,6,7-tetrabromobenzotriazole (TBB), a CK2-specific inhibitor, attenuated ER stress-induced XBP-1 splicing and subsequent induction of GRP78 expression, but was ineffective against ER stress-induced eIF2 alpha phosphorylation and CHOP expression. Similar results were obtained when endogenous CK2 expression was knocked-down by siRNA. Immunohistochemical analysis suggested that CK2 was present at the ER. These results indicate CK2 to be linked with UPR and to resist ER stress by activating the XBP-1-GRP78 arm of UPR.
言語 en
出版者
出版者 Public Library of Science
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 VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ DOI
関連識別子 10.1371/journal.pone.0040144
関連情報
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1371/journal.pone.0040144
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1932-6203
開始ページ
開始ページ e40144
書誌情報 PLoS ONE
PLoS ONE

巻 7, 号 6, p. e40144, 発行日 2012
旧ID 34760
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