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Induction of apoptosis by accelerated heavy-ion beams in cultured fetal rat testes and its modification

https://repo.qst.go.jp/records/62645
https://repo.qst.go.jp/records/62645
93b26ec8-1782-4a69-938f-d0038729aebd
Item type 会議発表用資料 / Presentation(1)
公開日 2008-07-24
タイトル
タイトル Induction of apoptosis by accelerated heavy-ion beams in cultured fetal rat testes and its modification
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 Bing, Wang

× Bing, Wang

WEKO 618886

Bing, Wang

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Tanaka, Kaoru

× Tanaka, Kaoru

WEKO 618887

Tanaka, Kaoru

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Shang, Yi

× Shang, Yi

WEKO 618888

Shang, Yi

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Fujita, Kazuko

× Fujita, Kazuko

WEKO 618889

Fujita, Kazuko

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Ninomiya, Yasuharu

× Ninomiya, Yasuharu

WEKO 618890

Ninomiya, Yasuharu

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Moreno, Stephanie.G

× Moreno, Stephanie.G

WEKO 618891

Moreno, Stephanie.G

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Herve, Coffigny

× Herve, Coffigny

WEKO 618892

Herve, Coffigny

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Hayata, Isamu

× Hayata, Isamu

WEKO 618893

Hayata, Isamu

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Murakami, Masahiro

× Murakami, Masahiro

WEKO 618894

Murakami, Masahiro

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Eguchi-Kasai, Kiyomi

× Eguchi-Kasai, Kiyomi

WEKO 618895

Eguchi-Kasai, Kiyomi

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Nenoi, Mitsuru

× Nenoi, Mitsuru

WEKO 618896

Nenoi, Mitsuru

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王 冰

× 王 冰

WEKO 618897

en 王 冰

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田中 薫

× 田中 薫

WEKO 618898

en 田中 薫

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尚 奕

× 尚 奕

WEKO 618899

en 尚 奕

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藤田 和子

× 藤田 和子

WEKO 618900

en 藤田 和子

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二宮 康晴

× 二宮 康晴

WEKO 618901

en 二宮 康晴

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早田 勇

× 早田 勇

WEKO 618902

en 早田 勇

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村上 正弘

× 村上 正弘

WEKO 618903

en 村上 正弘

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笠井 清美

× 笠井 清美

WEKO 618904

en 笠井 清美

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根井 充

× 根井 充

WEKO 618905

en 根井 充

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抄録
内容記述タイプ Abstract
内容記述 The increasing human activities in space missions make the study on effects from high-LET ionizing radiation an important issue to be addressed. We reported previously that prenatal irradiations with heavy-ion beams on gestation day 15 generally induced markedly detrimental effects on prenatal gonads, postnatal testicular development and male breeding activity in rats. To explore the mechanisms involved in radiation-induced gonocyte apoptosis in fetal gonads, which played a critical role in the fate of postnatal testis development, accelerated heavy-ion irradiations and organotypic culture of Wistar fetal rat testes were applied to investigations focused on cellular and molecular events after irradiations with or without chemical addition. Results showed that, in addition to the clustered distribution, both the time course and the percentage of apoptosis in gonocytes on gestation day 15 equivalent in vitro appeared similar to that in utero after exposure to either carbon-ion beams with a LET value of about 13 keV/mu m or neon-ion beams with a LET value of about 30 keV/mu m. Irradiations induced increased p53 expression in a dose dependent manner and decreased expressions of p21 and Bcl-2 by Western Blot examination. Administration of pan-caspase inhibitor prior to irradiations effectively inhibited apoptosis occurrence and reduced the extent of clustered apoptosis, while such effects were not observed with the presence of p53 inhibitor, gap junction inhibitor, or nitric oxide specific scavenger. These findings indicated that irradiations of cultured fetal rat testes manifested pathologically similar apoptosis induction in gonocytes to that in utero. P53 expression was possibly responsible for the response to radiation damage rather than induction of apoptosis. The syncytial organization of gonocytes played a key role in formation of the clustered apoptosis, an event that both gap junction inhibitor and nitric oxide specific scavenger were incapable of preventing.
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 COSPAR Scientific Assembly
発表年月日
日付 2008-07-20
日付タイプ Issued
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