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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)

Signalling pathway involving GULP, MAPK and Rac1 for SR-BI-induced phagocytosis of apoptotic cells.

http://hdl.handle.net/2297/18196
http://hdl.handle.net/2297/18196
3fc50955-6b90-4938-b31a-423061ce885e
名前 / ファイル ライセンス アクション
PH-PR-NAKANISHI-Y-387.pdf PH-PR-NAKANISHI-Y-387.pdf (242.0 kB)
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 Signalling pathway involving GULP, MAPK and Rac1 for SR-BI-induced phagocytosis of apoptotic 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 Osada, Yoichi

× Osada, Yoichi

WEKO 27921

Osada, Yoichi

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Sunatani, Toshiro

× Sunatani, Toshiro

WEKO 27922

Sunatani, Toshiro

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Kim, In-San

× Kim, In-San

WEKO 27923

Kim, In-San

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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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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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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 145, 号 3, p. 387-394, 発行日 2009-03-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 1756-2651
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1093/jb/mvn176
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 Class B scavenger receptor type I (SR-BI) is a phosphatidylserine (PS)-recognizing receptor of testicular Sertoli cells responsible for the phagocytosis of spermatogenic cells undergoing apoptosis. Here, we determined signal mediators that compose a signalling pathway for SR-BI-induced phagocytosis. Results of a yeast two-hybrid analysis and a cell-free binding assay indicated that SR-BI binds to engulfment adapter protein (GULP) using the C-terminal intracellular domain. A co-immunoprecipitation analysis showed the existence of a complex of GULP and SR-BI in cells prior to the activation of SR-BI by PS. A reduction of GULP expression in phagocytes decreased the SR-BI-mediated phagocytosis of apoptotic cells. Administration to phagocytes of PS-containing liposomes increased the levels of the GTP-bound form of Rac1 and the phosphorylated forms of mitogen-activated protein kinases (MAPK) p38 and extracellular signal-related kinase 1 and 2. Finally, lowering the expression of GULP abrogated MAPK phosphorylation, and the presence of MAPK inhibitors reduced the level of GTP-bound Rac1 in PS-activated phagocytes. These results collectively suggested the following signalling pathway for the SR-BI-induced phagocytosis: (i) PS-recognizing SR-BI activates associated GULP; (ii) activated GULP induces MAPK phosphorylation; (iii) activated MAPK increases GTP-bound Rac1; and (iv) activated Rac1 induces a rearrangement of the actin cytoskeleton.
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連URI
識別子タイプ URI
関連識別子 http://jb.oxfordjournals.org/cgi/content/abstract/145/3/387
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