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  1. 原著論文

Nemo-like kinase (NLK) expression in osteoblastic cells and suppression of osteoblastic differentiation.

https://repo.qst.go.jp/records/46125
https://repo.qst.go.jp/records/46125
391772ca-debf-4821-98cb-e79f3211f79f
Item type 学術雑誌論文 / Journal Article(1)
公開日 2011-07-14
タイトル
タイトル Nemo-like kinase (NLK) expression in osteoblastic cells and suppression of osteoblastic differentiation.
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 Nifuji, Akira

× Nifuji, Akira

WEKO 459213

Nifuji, Akira

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Ideno, Hisashi

× Ideno, Hisashi

WEKO 459214

Ideno, Hisashi

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Ohyama, Yoshio

× Ohyama, Yoshio

WEKO 459215

Ohyama, Yoshio

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Takanabe, Rieko

× Takanabe, Rieko

WEKO 459216

Takanabe, Rieko

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Araki, Ryoko

× Araki, Ryoko

WEKO 459217

Araki, Ryoko

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Abe, Masumi

× Abe, Masumi

WEKO 459218

Abe, Masumi

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Noda, Masaki

× Noda, Masaki

WEKO 459219

Noda, Masaki

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Shibuya, Hiroshi

× Shibuya, Hiroshi

WEKO 459220

Shibuya, Hiroshi

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二藤 彰

× 二藤 彰

WEKO 459221

en 二藤 彰

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出野 尚

× 出野 尚

WEKO 459222

en 出野 尚

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高鍋 利依子

× 高鍋 利依子

WEKO 459223

en 高鍋 利依子

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荒木 良子

× 荒木 良子

WEKO 459224

en 荒木 良子

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安倍 真澄

× 安倍 真澄

WEKO 459225

en 安倍 真澄

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抄録
内容記述タイプ Abstract
内容記述 Mitogen-activated protein kinases (MAPKs) regulate proliferation and differentiation in osteoblasts. The vertebral homologue of nemo, nemo-like kinase (NLK), is an atypical MAPK that targets several signaling components, including the T-cell factor/lymphoid enhancer factor (TCF/Lef1) transcription factor. Recent studies have shown that NLK forms a complex with the histone H3-K9 methyltransferase SETDB1 and suppresses peroxisome proliferator-activated receptor (PPAR)-gamma:: action in the mesenchymal cell line ST2. Here we investigated whether NLK regulates osteoblastic differentiation. We showed that NLK mRNA is expressed in vivo in osteoblasts at embryonic day 18.5 (E18.5) mouse calvariae. By using retrovirus vectors, we performed forced expression of NLK in primary calvarial osteoblasts (pOB cells) and the mesenchymal cell line ST2. Wild-type NLK (NLK-WT) suppressed alkaline phosphatase activity and expression of bone marker genes such as alkaline phosphatase, type I procollagen, runx2, osterix, steopontin and osteocalcin in these cells. NLK-WT also decreased type I collagen protein expression in pOB and ST2 cells. Furthermore, mineralized nodule formation was reduced in pOB cells overexpressing NLK-WT. In contrast, kinase-negative form of NLK (NLK-KN) did not suppress or partially suppress ALP activity and bone marker gene expression in pOB and ST2 cells. NLK-KN did not suppress nodule formation in pOB cells. In addition to forced expression, suppression of endogenous NLK expression by siRNA increased bone marker gene expression in pOB and ST2 cells. Finally, transcriptional activity analysis of gene promoters revealed that NLK-WT suppressed Wnt1 activation of TOP flash promoter and Runx2 activation of the osteocalcin promoter. Taken together, these results suggest that NLK negatively regulates osteoblastic differentiation.
書誌情報 Experimental Cell Research

巻 316, 号 7, p. 1127-1136, 発行日 2010-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0014-4827
DOI
識別子タイプ DOI
関連識別子 10.1016/j.yexcr.2010.01.023
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