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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 2.査読済論文(薬)

Structural change of ribosomes during apoptosis: Degradation and externalization of ribosomal proteins in doxorubicin-treated Jurkat cells

http://hdl.handle.net/2297/14554
http://hdl.handle.net/2297/14554
33efc0f9-f4ef-4a5f-b07a-8dc816de0394
名前 / ファイル ライセンス アクション
PH-PR-NAKANISHI-Y-485.pdf PH-PR-NAKANISHI-Y-485.pdf (5.5 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-04
タイトル
タイトル Structural change of ribosomes during apoptosis: Degradation and externalization of ribosomal proteins in doxorubicin-treated Jurkat cells
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
著者 Nishida, Jun

× Nishida, Jun

WEKO 27722

Nishida, Jun

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Shiratsuchi, Akiko

× Shiratsuchi, Akiko

WEKO 27298
金沢大学研究者情報 90303297
研究者番号 90303297

Shiratsuchi, Akiko

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Nadano, Daita

× Nadano, Daita

WEKO 27723

Nadano, Daita

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Sato, Takaaki

× Sato, Takaaki

WEKO 27724

Sato, Takaaki

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Nakanishi, Yoshinobu

× Nakanishi, Yoshinobu

WEKO 103
e-Rad 40172358
金沢大学研究者情報 40172358
研究者番号 40172358

Nakanishi, Yoshinobu

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提供者所属
内容記述タイプ Other
内容記述 金沢大学医薬保健研究域薬学系
書誌情報 Journal of Biochemistry

巻 131, 号 3, p. 485-493, 発行日 2002-01-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0021-924X
NCID
収録物識別子タイプ NCID
収録物識別子 AA00694073
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1093/oxfordjournals.jbchem.a003125
出版者
出版者 日本生化学会 = Japanese Biochemical Society
抄録
内容記述タイプ Abstract
内容記述 Changes in the amount and localization of human ribosomal proteins during apoptosis were determined. When total lysates of Jurkat cells undergoing apoptosis induced by doxorubicin were analyzed by Western blotting, degradation of three ribosomal proteins, S18, L5, and L14, was detected at 48 h after the induction of apoptosis. Decreases in the amounts of these three ribosomal proteins were also observed in ribosome-enriched fractions. These changes were partly abolished by the addition of the pan-caspase inhibitor z-VAD-fmk. Moreover, formation of the 80S ribosome complex appeared to be inhibited at 48 h after apoptosis induction. On the other hand, the rate of protein synthesis, assessed by measuring the incorporation of [35S]Met into bulk proteins, decreased as early as 12 h after the addition of doxorubicin. These results indicate that changes in the amount of ribosomal proteins and the overall structure of ribosomes in apoptosing cells occur after protein synthesis declines. Finally, analyses by flow cytometry, immunofluorescence, and Western blotting showed that six ribosomal proteins, S15, PO, L5, L6, L36a, and L41, were relocalized and expressed at the cell surface during apoptosis. The above results collectively indicate that ribosomes are structurally altered in apoptotic cells following inactivation of protein synthesis.
権利
権利情報 Copyright © 2002 Japanese Biochemical Society
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
関連URI
識別子タイプ URI
関連識別子 http://jb.oxfordjournals.org/cgi/content/abstract/131/3/485
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