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CNP Receptor Gene (Npr2) is Involved in the Regulation of Blood-Testis Barrier and Spermatogenesis in Mouse

https://repo.qst.go.jp/records/71005
https://repo.qst.go.jp/records/71005
4a9e5d8a-842e-4dfe-a709-1f2c9687e422
Item type 会議発表用資料 / Presentation(1)
公開日 2012-12-10
タイトル
タイトル CNP Receptor Gene (Npr2) is Involved in the Regulation of Blood-Testis Barrier and Spermatogenesis in Mouse
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 Sogawa, Chizuru

× Sogawa, Chizuru

WEKO 697888

Sogawa, Chizuru

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Tsukamoto, Satoshi

× Tsukamoto, Satoshi

WEKO 697889

Tsukamoto, Satoshi

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Ishida, Yuka

× Ishida, Yuka

WEKO 697890

Ishida, Yuka

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Yoshii, Yukie

× Yoshii, Yukie

WEKO 697891

Yoshii, Yukie

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Furukawa, Takako

× Furukawa, Takako

WEKO 697892

Furukawa, Takako

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KUNIEDA, Tetsuo

× KUNIEDA, Tetsuo

WEKO 697893

KUNIEDA, Tetsuo

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 697894

Saga, Tsuneo

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et.al

× et.al

WEKO 697895

et.al

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曽川 千鶴

× 曽川 千鶴

WEKO 697896

en 曽川 千鶴

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塚本 智史

× 塚本 智史

WEKO 697897

en 塚本 智史

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石田 有香

× 石田 有香

WEKO 697898

en 石田 有香

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吉井 幸恵

× 吉井 幸恵

WEKO 697899

en 吉井 幸恵

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古川 高子

× 古川 高子

WEKO 697900

en 古川 高子

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佐賀 恒夫

× 佐賀 恒夫

WEKO 697901

en 佐賀 恒夫

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抄録
内容記述タイプ Abstract
内容記述 C-type natriuretic peptide (CNP) exerts its main biological effects by binding to natriuretic peptide receptor B (NPR-B), a membrane-bound guanylyl cyclase receptor that produces cyclic guanosine monophosphate (cGMP). It was previously reported that cGMP induced by nitric oxide via soluble guanylyl cyclase regulates Sertoli cell tight junction in vitro and permeability of the blood-testis barrier (BTB) which separates the seminiferous epithelium into the adluminal and basal compartments during spermatogenesis. Furthermore, it was also reported that CNP regulates BTB dynamics in adult rat testes.
We recently reported that the short-limbed dwarfism (SLW) mouse has a mutation in Npr-2 gene, which encodes NPR-B and this mutation results in deletion of the intracellular domain of NPR-B. However, the effect of the flaw in the NPR-B-induced cGMP production through CNP signal against spermatogenesis has not yet been demonstrated. Therefore, the aim of this study is to elucidate the function of NPR-B in the progression of spermatogenesis in mouse.
We first examined the immunohistochemical distribution of NPR-B in the seminiferous epithelium of the normal mouse testis during the first-wave of spermatogenesis. NPR-B was initially expressed within a spermatogonium, and subsequently located to the cytoplasm of a spermatocyte and a round spermatid predominantly in the normal testes. We next examined the phenotype of testes in SLW mice. It was revealed that the testis of slw/slw homozygotes showed retardation of spermatogenic development in 2w and vacuolation in the seminiferous epithelium in 3w. Immunohistochemical staining of ZO-1, a tight junction protein revealed that BTB was located in a boundary between the basement and the lumen in the seminiferous epithelium of 2w normal testis, whereas BTB formation was disordered and misaligned in the 2w slw/slw.
These results suggest that NPR-B mediated cGMP production through CNP signal has a role important for BTB regulation which is required for spermatogenesis.
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 58th/60th NIBB Conferenc
発表年月日
日付 2012-07-21
日付タイプ Issued
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