The EP4-ERK-dependent pathway stimulates osteo-adipogenic progenitor proliferation resulting in increased adipogenesis in fetal rat calvaria cell cultures
Prostaglandins & Other Lipid Mediators 97 巻 3-4 号
97-102 頁
2012-03 発行
アクセス数 : 665 件
ダウンロード数 : 102 件
今月のアクセス数 : 6 件
今月のダウンロード数 : 1 件
この文献の参照には次のURLをご利用ください : https://ir.lib.hiroshima-u.ac.jp/00049713
ファイル情報(添付) |
ProstaglandinsOtherLipidMediat_97_97.pdf
1.21 MB
種類 :
全文
|
タイトル ( eng ) |
The EP4-ERK-dependent pathway stimulates osteo-adipogenic progenitor proliferation resulting in increased adipogenesis in fetal rat calvaria cell cultures
|
作成者 |
Aubin Jane E.
Maeda Norihiko
|
収録物名 |
Prostaglandins & Other Lipid Mediators
|
巻 | 97 |
号 | 3-4 |
開始ページ | 97 |
終了ページ | 102 |
抄録 |
We previously reported that fetal rat calvaria (RC) cells are osteo-adipogenic bipotential and that PGE2 receptors EP2 and EP4 are involved in bone nodule formation via both common and distinct MAPK pathways in RC cell cultures. Because PGE2 participates in multiple biological processes including adipogenesis, it is of interest to determine the additional role(s) of PGE2 in RC cells. PGE2 increased the number of adipocyte colonies when RC cells were treated during proliferation but not other development stages. Of four EP agonists tested, the EP4 agonist ONO-AE1-437 (EP4A) was the most effective in promoting adipogenesis. Concomitantly, EP4A increased the number of cells with BrdU labeling and gene expression of CCAAT/enhancer binding protein (C/EBP)δ and c-fos but not peroxisome proliferator-activated receptor γ2 and C/EBPα. Amongst MAPK inhibitors, U0126, an inhibitor of MEK1/2, abrogated the EP4A-dependent effects. Our results suggest that the PGE2–EP4-ERK pathway increases the number of osteo-adipogenic bipotential progenitor cells, with a resultant increase in adipogenesis in RC cell cultures.
|
著者キーワード |
Selective EP agonists
Rat calvaria cells
Osteogenesis
Adipogenesis
ERK pathway
|
内容記述 |
This work was supported in part by grants from the Ministry of Education, Science, Sports and Culture of Japan (13771074 to YY)and Ono Pharmaceutical Co. (to YY), and the Canadian Institutes of Health Research (CIHR; FRN 83704 to JEA).
|
言語 |
英語
|
資源タイプ | 学術雑誌論文 |
出版者 |
Elsevier
|
発行日 | 2012-03 |
権利情報 |
© 2012. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
This is not the published version. Please cite only the published version. この論文は出版社版ではありません。引用の際には出版社版をご確認、ご利用ください。
|
出版タイプ | Author’s Original(十分な品質であるとして、著者から正式な査読に提出される版) |
アクセス権 | オープンアクセス |
収録物識別子 |
[ISSN] 1098-8823
[DOI] 10.1016/j.prostaglandins.2012.01.001
[PMID] 22265865
[DOI] https://doi.org/10.1016/j.prostaglandins.2012.01.001
|