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Analysis in expression of CD180 molecules on spleen cells after radiation-induced apoptosis in vivo

https://repo.qst.go.jp/records/71007
https://repo.qst.go.jp/records/71007
ac6d4988-94cb-46cf-95b8-50ea71a168de
Item type 会議発表用資料 / Presentation(1)
公開日 2012-12-11
タイトル
タイトル Analysis in expression of CD180 molecules on spleen cells after radiation-induced apoptosis in vivo
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 Fujita, Kazuko

× Fujita, Kazuko

WEKO 697904

Fujita, Kazuko

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Kuwabara, Taku

× Kuwabara, Taku

WEKO 697905

Kuwabara, Taku

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Bing, Wang

× Bing, Wang

WEKO 697906

Bing, Wang

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Tanaka, Kaoru

× Tanaka, Kaoru

WEKO 697907

Tanaka, Kaoru

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Akasaka, Yosikiyo

× Akasaka, Yosikiyo

WEKO 697908

Akasaka, Yosikiyo

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Ishii, Toshiharu

× Ishii, Toshiharu

WEKO 697909

Ishii, Toshiharu

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藤田 和子

× 藤田 和子

WEKO 697910

en 藤田 和子

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桑原 卓

× 桑原 卓

WEKO 697911

en 桑原 卓

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王 冰

× 王 冰

WEKO 697912

en 王 冰

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田中 薫

× 田中 薫

WEKO 697913

en 田中 薫

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抄録
内容記述タイプ Abstract
内容記述 The CD180 molecule is a receptor of LPS on mature B cell and a homologue of TLR 4, and regulates TLR 4 negatively. The molecule has a protective effect against radiation- or dexamethasone-induced apoptosis in vitro. Antibody-mediated cross-linkingof CD180 induces a strong proliferative response, and secondary cross-linking of surface IgM induces B cell apoptosis in vitro. CD180 is thus a key regulator of proliferation and cell death. However, few studies regarding the functional mechanism of the CD180 molecule associated with radiation-induced apoptosis have been reported in vivo. In the present study, we have examined the effect of irradiation on the expression patterns of CD180 of spleen cell and compared with that of CD19 and CD21 on B cell in vivo. Spleens of BALB/c female mice at 7-8 weeks were removed after whole body-irradiation of 4 Gy. Histochemical analysis demonstrated that CD180-positive lymphocytes significantly increased in number at 6 h after irradiation compared with both at 3 h and 0 h. In contrast, no significant change of the numbers of lymphocytes positive for CD19 or CD22 was at 0 h, 3 h, and 6 h after irradiation. Flow cytometric analysis showed that the percentage of CD180-presenting B cells increased at 6 h after irradiation than that at 0 h. As the expression of CD180 was increased dependently on radiation dose from 0 Gy to 10 Gy and on the level of apoptosis with histochemical analysis, double staining for TUNEL and CD180 was performed to clarify the relationship of the expression patterns between apoptosis and CD180. The double staining showed that the number of CD180-positive cells positive for TUNEL was significantly less than that of CD180-negative cells positive for TUNEL at 6 h after irradiation. These results suggested that CD180- positive B lymphocytes were resistant to apoptosis induced by irradiation in vivo.
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 第41回日本免疫学会学術集会
発表年月日
日付 2012-12-07
日付タイプ Issued
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