Inhibition of myoblast differentiation by Sfrp1 and Sfrp2

被引:45
|
作者
Descamps, Simon [1 ,2 ]
Arzouk, Hayat [1 ]
Bacou, Francis [1 ]
Bernardi, Henri [1 ]
Fedon, Yann [1 ]
Gay, Stephanie [1 ]
Reyne, Yves [1 ]
Rossano, Bernadette [1 ]
Levin, Jonathan [1 ]
机构
[1] INRA, UMR Differenciat Cellulaire & Croissance 866, F-34060 Montpellier, France
[2] Univ Montpellier 2, F-34095 Montpellier, France
关键词
Sfrp1; Sfrp2; myoblast; proliferation; differentiation; cell culture; mouse; rabbit;
D O I
10.1007/s00441-008-0574-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Secreted Frizzled-related proteins (Sfrps) are extracellular regulators of Wnt signalling and play important roles in developmental and oncogenic processes. They are known to be upregulated in regenerating muscle and in myoblast cultures but their function is unknown. Here, we show that the addition of recombinant Sfrp1 or Sfrp2 to C2C12 cell line cultures or to primary cultures of satellite cells results in the inhibition of myotube formation with no significant effect on the cell cycle or apoptosis. Even though at confluence, treated and untreated cultures are identical in appearance, analyses have shown that, for maximum effect, the cells have to be treated while they are proliferating. Furthermore, removal of Sfrp from the culture medium during differentiation restores normal myotube formation. We conclude that Sfrp1 and Sfrp2 act to prevent myoblasts from entering the terminal differentiation process.
引用
收藏
页码:299 / 306
页数:8
相关论文
共 50 条
  • [21] Wnt通路拮抗基因SFRP1 SFRP2 SFRP4 SFRP5甲基化状态与肾透明细胞癌关系的研究
    张爱莉
    殷凤朝
    赵志红
    倪晓辰
    [J]. 中国肿瘤临床, 2011, 38 (19) : 1179 - 1182
  • [22] 胃癌患者SFRP1、SFRP2、SDC-2甲基化与病理特征的相关性分析
    黄一波
    王国平
    王奕
    莫文魁
    [J]. 中华全科医学, 2021, 19 (12) : 2008 - 2011
  • [23] Genetic Instability in the Downregulation of sFRP1
    Watanabe, Toshiaki
    Matsuda, Keiji
    Ishihara, Soichiro
    Nozawa, Keijiro
    Hayama, Tamuro
    Yamada, Hideki
    Kobunai, Takashi
    [J]. ANATOMICAL RECORD-ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY, 2011, 294 (08):
  • [24] Wnt拮抗基因SFRP1、SFRP2启动子区甲基化与贲门腺癌关系的研究
    董稚明
    王馥丽
    靳国梁
    郭炜
    郭艳丽
    王士杰
    [J]. 肿瘤研究与临床, 2009, (12)
  • [25] Comparative genomics on SFRP2 orthologs
    Katoh, M
    Katoh, M
    [J]. ONCOLOGY REPORTS, 2005, 14 (03) : 783 - 787
  • [26] A role for Sfrp2 in cardiomyogenesis in vivo
    Gomez, Jose A.
    Payne, Alan
    Pratt, Richard E.
    Hodgkinson, Conrad P.
    Dzau, Victor J.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2021, 118 (33)
  • [27] Mutations in SFRP1 or SFRP4 are not a common cause of craniotubular hyperostoses
    Boudin, E.
    Piters, E.
    Fijalkowski, I.
    Stevenheydens, G.
    Van Hul, W.
    [J]. BONE, 2012, 50 : S106 - S107
  • [28] Comparative genomics on SFRP1 orthologs
    Katoh, Y
    Katoh, M
    [J]. INTERNATIONAL JOURNAL OF ONCOLOGY, 2005, 27 (03) : 861 - 865
  • [29] Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis
    Boudin, Eveline
    Piters, Elke
    Fijalkowski, Igor
    Stevenheydens, Gino
    Steenackers, Ellen
    Kuismin, Outi
    Moilanen, Jukka S.
    Mortier, Geert
    Van Hul, Wim
    [J]. BONE, 2013, 52 (01) : 292 - 295
  • [30] Sfrp1 and Sfrp2 are not involved in Wnt/β-catenin signal silencing during lens induction but are required for maintenance of Wnt/β-catenin signaling in lens epithelial cells
    Sugiyama, Yuki
    Shelley, Elizabeth J.
    Wen, Li
    Stump, Richard J. W.
    Shimono, Akihiko
    Lovicu, Frank J.
    McAvoy, John W.
    [J]. DEVELOPMENTAL BIOLOGY, 2013, 384 (02) : 181 - 193