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  1. 川崎医学会機関誌
  2. 川崎医学会誌
  3. Vol.39(2013)
  4. No.1

Genistein affects osteoblastic MC3T3-E1 cells both through estrogen receptor and BMP-Smad signaling pathways

https://kwmed.repo.nii.ac.jp/records/1631
https://kwmed.repo.nii.ac.jp/records/1631
9114b49a-28ce-470c-b04f-2ba14aa714aa
名前 / ファイル ライセンス アクション
KJ00008396999.pdf KJ00008396999.pdf (614.9 kB)
Item type [ELS]学術雑誌論文 / Journal Article(1)
公開日 2017-01-23
タイトル
タイトル Genistein affects osteoblastic MC3T3-E1 cells both through estrogen receptor and BMP-Smad signaling pathways
言語 en
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
著者 Hinenoya, Hajime

× Hinenoya, Hajime

en Hinenoya, Hajime

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Katsuyama, Hironobu

× Katsuyama, Hironobu

en Katsuyama, Hironobu

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Nohno, Tsutomu

× Nohno, Tsutomu

en Nohno, Tsutomu

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著者所属(英)
en
Department of Public Health, Kawasaki Medical School
著者所属(英)
en
Department of Public Health, Kawasaki Medical School
著者所属(英)
en
Department of Molecular and Developmental Biology, Kawasaki Medical School
キーワード
言語 en
主題Scheme Other
主題 Genistein
キーワード
言語 en
主題Scheme Other
主題 Osteoprotegerin
キーワード
言語 en
主題Scheme Other
主題 BMP-Smad signaling
キーワード
言語 en
主題Scheme Other
主題 MC3T3-E1 cells
記事種別(日)
内容記述タイプ Other
内容記述 原著
言語 ja
抄録(英)
en
Many epidemiological studies show that genistein intake is effective for maintaining bone mineral density (BMD). Because the reason for the efficacy of genistein as a bone protective agent in vivo remains unclear, we investigated the mechanisms underlying the effects of genistein on BMD in relation to BMP-Smad signaling systems. When osteoblastic MC3T3-E1 cells were exposed to 1 μM genistein, they increased in number. Combined administrations of 1 μM genistein and 1 μM of ICI 182,780 inhibited the increase in cell numbers. Alkaline phosphatase (ALP) and Alizarin red staining showed high activities, indicating that genistein might promote estrogenic differentiation of MC3T3-E1 cells. Moreover, ELISA determined that production of osteoprotegerin (OPG), which is expressed by osteoblasts, was higher when 1 μM genistein was added to the medium than in controls. In contrast, when 10 ng/mL of noggin was administered in the medium, OPG production was inhibited. In order to clarify the underlying mechanism, we investigated the BMP-Smad signaling pathway. When genistein was added to the medium, it induced gene expression of BMP-4. Immunofluorescence staining showed that genistein induced phosphorylation of Smad 1/5, a downstream molecule of BMP. When noggin, which binds to BMP and blocks BMP signaling, was added to the medium, phosphorylation of Smad 1/5 was reduced. These results indicate that genistein may regulate bone metabolism through the BMP-Smad signaling pathway as well as through the estrogen receptor pathway.
書誌情報 ja : 川崎医学会誌
en : Kawasaki medical journal

巻 39, 号 1, p. 21-31, 発行日 2013
URL
識別子 http://igakkai.kms-igakkai.com/wp/wp-content/uploads/2013/KMJ31(1)21-31.2013.pdf
識別子タイプ URI
DOI
識別子タイプ DOI
関連識別子 https://doi.org/10.11482/2013/KMJ31(1)21-31.2013.pdf
ISSN
収録物識別子タイプ PISSN
収録物識別子 0386-5924
ISSN
収録物識別子タイプ EISSN
収録物識別子 2758-089X
雑誌書誌ID
収録物識別子タイプ NCID
収録物識別子 AN00045593
雑誌書誌ID
収録物識別子タイプ NCID
収録物識別子 AN12940574
著者版フラグ
出版タイプ VoR
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