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  1. 原著論文

Hydrogen peroxide as a potential mediator of the transcriptional regulation of heparan sulphate biosynthesis in keratinocytes.

https://repo.qst.go.jp/records/48387
https://repo.qst.go.jp/records/48387
dfde88db-bda6-4158-a14c-4635a39922a5
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-11-22
タイトル
タイトル Hydrogen peroxide as a potential mediator of the transcriptional regulation of heparan sulphate biosynthesis in keratinocytes.
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
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 486334

Nakayama, Fumiaki

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Hagiwara, Akiko

× Hagiwara, Akiko

WEKO 486335

Hagiwara, Akiko

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Yamamoto, Tetuo

× Yamamoto, Tetuo

WEKO 486336

Yamamoto, Tetuo

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Akashi, Makoto

× Akashi, Makoto

WEKO 486337

Akashi, Makoto

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中山 文明

× 中山 文明

WEKO 486338

en 中山 文明

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萩原 亜紀子

× 萩原 亜紀子

WEKO 486339

en 萩原 亜紀子

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山本 哲生

× 山本 哲生

WEKO 486340

en 山本 哲生

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明石 真言

× 明石 真言

WEKO 486341

en 明石 真言

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抄録
内容記述タイプ Abstract
内容記述 Ionizing radiation is one of the types of oxidative stress that has a number of damaging effects on cutaneous tissues. One of the histological features of radiation-induced cutaneous fibrosis is the accumulation of extracellular matrix (ECM) components, including heparan sulfate proteoglycan (HSPG), which are required for the repair of tissue damage, and operate by interacting with a variety of growth factors. In this study, we established a model of human HaCaT keratinocytes overexpressing anti-oxidative enzyme genes to elucidate the mechanism of oxidative stress leading to the accumulation of HSPG and the role of its accumulation. Catalase overexpression induced an increase in anti-HS antibody (10E4) epitope expression in these cells. Western blotting showed that the smeared bands of HSPG were obviously shifted to a higher molecular weight in the catalase transfectants due to glycosylation. After heparitinase I treatment, the core proteins of HSPG were expressed in the catalase transfectants to almost the same extent as in the control cells. In addition, the transcript levels of all the enzymes required for the synthesis of the heparan sulfate chain were estimated in the catalase transfectant clones. The levels of five enzyme transcripts - xylosyltransferase-II (XT-II), EXTL2, D-glucuronyl C5-epimerase (GLCE), HS2-O-sulfotransferase (HS2ST), and HS6-O-sulfotransferase (HS6ST) - were significantly increased in the transfectants. Moreover, hydrogen peroxide was found to down-regulate the levels of these enzymes. By contrast, siRNA-mediated repression of catalase decreased 10E4 epitope expression, the transcript level of HS2ST1, and the growth rate of HaCaT cells. These findings suggested that peroxide-mediated transcriptional regulation of HS metabolism-related genes modified the HS chains in the HaCaT keratinocytes.
書誌情報 Cellular & Molecular Biology Letters

巻 13, 号 3, p. 475-492, 発行日 2008-09
ISSN
収録物識別子タイプ ISSN
収録物識別子 1425-8153
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