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Anti-oxidative enzyme catalase controls proliferation of HaCaT cells through the regulation of heparan sulfate 2-O-sulfotransferase

https://repo.qst.go.jp/records/69252
https://repo.qst.go.jp/records/69252
f999fc92-684c-4276-b2c9-1858ceb134a3
Item type 会議発表用資料 / Presentation(1)
公開日 2007-12-27
タイトル
タイトル Anti-oxidative enzyme catalase controls proliferation of HaCaT cells through the regulation of heparan sulfate 2-O-sulfotransferase
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_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Nakayama, Fumiaki

× Nakayama, Fumiaki

WEKO 679548

Nakayama, Fumiaki

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Hagiwara, Akiko

× Hagiwara, Akiko

WEKO 679549

Hagiwara, Akiko

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Akashi, Makoto

× Akashi, Makoto

WEKO 679550

Akashi, Makoto

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中山 文明

× 中山 文明

WEKO 679551

en 中山 文明

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萩原 亜紀子

× 萩原 亜紀子

WEKO 679552

en 萩原 亜紀子

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明石 真言

× 明石 真言

WEKO 679553

en 明石 真言

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抄録
内容記述タイプ Abstract
内容記述 Heparan sulfate (HS) chains can interact with a variety of growth factors possessing heparin-binding domains, such as fibroblast growth factors (FGFs), enabling them to transfer to their high-affinity signaling receptors on the cell surface. In this study, we demonstrated the correlation between the expression of anti-oxidative enzymes and the HS chain in the human HaCaT keratinocyte cell line. The overexpression of catalase induced an increase of anti-HS antibody (10E4) epitope expression in these cells; however the MnSOD transfectant expressed it at the same level as the control cells. Western blotting showed that the smeared bands of HSPG were obviously shifted to higher-molecular-weight in the catalase transfectants owing to glycosylation. The levels of glycosyltransferases (XT-II, EXTL2, GLCE, HS2ST1 and HS6ST1) transcripts were significantly increased in the transfectants. In contrast, siRNA-mediated repression of catalase decreased 10E4 epitope expression, the transcript level of HS2ST1, and proliferation of HaCaT cells; however it did not significantly down-regulate the transcript level of HS6ST1. In addition, siRNA-mediated repression of HS2ST1 decreased HaCaT cell proliferation, although repression of HS6ST1 did not reduce it. These findings suggest that catalase may be able to modify the HS chains in the keratinocytes through the regulation of HS2ST1 to control HaCaT cell proliferation.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 37th Annual ESDR Meeting 2007
発表年月日
日付 2007-09-08
日付タイプ Issued
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