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  1. 原著論文

Detection of double-stranded DNA breaks and apoptosis induced by bleomycin in mouse intestine

https://repo.qst.go.jp/records/84668
https://repo.qst.go.jp/records/84668
43d85f2c-14b3-4ad3-9b28-fd051a70a1e2
Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-12-01
タイトル
タイトル Detection of double-stranded DNA breaks and apoptosis induced by bleomycin in mouse intestine
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 生田, 統悟

× 生田, 統悟

WEKO 1021873

生田, 統悟

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小池, 亜紀

× 小池, 亜紀

WEKO 1021874

小池, 亜紀

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小池, 学

× 小池, 学

WEKO 1021875

小池, 学

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Togo, Ikuta

× Togo, Ikuta

WEKO 1021876

en Togo, Ikuta

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Aki, Koike

× Aki, Koike

WEKO 1021877

en Aki, Koike

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Manabu, Koike

× Manabu, Koike

WEKO 1021878

en Manabu, Koike

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内容記述タイプ Abstract
内容記述 The gastrointestinal tract is exposed to a myriad of mutagens, making the DNA damage response (DDR) essential to maintain intestinal homeostasis. In vivo models to study DDRs are necessary to understand the mechanisms of disease development caused by genetic disorders such as colorectal cancer. A double-stranded break (DSB) in DNA is the most toxic type of DNA damage; it can be induced by either X-rays or chemicals, including anticancer agents. If DSBs in DNA cannot be repaired, cells can die by apoptosis to be removed from tissues. Here, we show that the DDRs observed as the phosphorylation of H2AX (γH2AX) and caspase-3-dependent apoptosis-induction are under critical control in the intestine of C57BL mice that were injected intraperitoneally with bleomycin, a natural glycopeptide used clinically as an antitumor agent. We found a significant increase in γH2AX expression 2–6 hr post-treatment in mouse ileum, cecum, and colon tissues by Western blotting and immunostaining. Apoptotic cells were observed after 6–24 hr by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay and immunofluorescence of active caspase-3. We observed that γH2AX expression and apoptotic cells were distributed in the lower part of the crypt. The experimental protocol described here is a simple procedure that can be used generally as an in vivo intestinal toxicity assay. Our experimental approach provides a useful method for examining the effects of various bioactive compounds on the DDR, which is essential for understanding intestinal homeostasis.
書誌情報 The Journal of Toxicological Sciences

巻 46, 号 12, p. 611-618, 発行日 2022-01
出版者
出版者 The Japanese Society of Toxicology
ISSN
収録物識別子タイプ ISSN
収録物識別子 0388-1350
DOI
識別子タイプ DOI
関連識別子 10.2131/jts.46.611
関連サイト
識別子タイプ URI
関連識別子 https://www.jstage.jst.go.jp/article/jts/46/12/46_611/_html/-char/en
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