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アイテム
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/46125391772ca-debf-4821-98cb-e79f3211f79f
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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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× Ideno, Hisashi× Ohyama, Yoshio× Takanabe, Rieko× Araki, Ryoko× Abe, Masumi× Noda, Masaki× Shibuya, Hiroshi× 二藤 彰× 出野 尚× 高鍋 利依子× 荒木 良子× 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 |
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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 |