BAMBI Promotes C2C12 Myogenic Differentiation by Enhancing Wnt/β-Catenin Signaling

被引:31
作者
Zhang, Qiangling [1 ]
Shi, Xin-E [1 ]
Song, Chengchuang [1 ]
Sun, Shiduo [1 ]
Yang, Gongshe [1 ]
Li, Xiao [1 ]
机构
[1] Northwest A&F Univ, Coll Anim Sci & Technol, Lab Anim Fat Deposit & Muscle Dev, Yangling 712100, Peoples R China
关键词
BAMBI; Wnt/beta-catenin; myogenic differentiation; LiCl; C2C12; BOUND INHIBITOR BAMBI; GROWTH-FACTOR-BETA; MOLECULAR-MECHANISM; NEGATIVE REGULATOR; PATHWAY; CELLS; ACTIVATION; BMP; IDENTIFICATION; TRANSCRIPTION;
D O I
10.3390/ijms160817734
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bone morphogenic protein and activin membrane-bound inhibitor (BAMBI) is regarded as an essential regulator of cell proliferation and differentiation that represses transforming growth factor- and enhances Wnt/-catenin signaling in various cell types. However, its role in skeletal muscle remains largely unknown. In the current study, we found that the expression level of BAMBI peaked in the early differentiation phase of the C2C12 rodent myoblast cell line. Knockdown of BAMBI via siRNA inhibited C2C12 differentiation, indicated by repressed MyoD, MyoG, and MyHC expression as well as reductions in the differentiation and fusion indices. BAMBI knockdown reduced the activity of Wnt/-catenin signaling, as characterized by the decreased nuclear translocation of -catenin and the lowered transcription of Axin2, which is a well-documented target gene of the Wnt/-catenin signaling pathway. Furthermore, treatment with LiCl, an activator of Wnt/-catenin signaling, rescued the reduction in C2C12 differentiation caused by BAMBI siRNA. Taken together, our data suggest that BAMBI is required for normal C2C12 differentiation, and that its role in myogenesis is mediated by the Wnt/-catenin pathway.
引用
收藏
页码:17734 / 17745
页数:12
相关论文
共 30 条
[1]   Building Muscle: Molecular Regulation of Myogenesis [J].
Bentzinger, C. Florian ;
Wang, Yu Xin ;
Rudnicki, Michael A. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2012, 4 (02)
[2]   A temporal switch from Notch to Wnt signaling in muscle stem cells is necessary for normal adult myogenesis [J].
Brack, Andrew S. ;
Conboy, Irina M. ;
Conboy, Michael J. ;
Shen, Jeanne ;
Rando, Thomas A. .
CELL STEM CELL, 2008, 2 (01) :50-59
[3]   Wnt Protein-mediated Satellite Cell Conversion in Adult and Aged Mice Following Voluntary Wheel Running [J].
Fujimaki, Shin ;
Hidaka, Ryo ;
Asashima, Makoto ;
Takemasa, Tohru ;
Kuwabara, Tomoko .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (11) :7399-7412
[4]   Regulation of the Follistatin Gene by RSPO-LGR4 Signaling via Activation of the WNT/β-Catenin Pathway in Skeletal Myogenesis [J].
Han, Xiang Hua ;
Jin, Yong-Ri ;
Tan, Leonard ;
Kosciuk, Tatiana ;
Lee, Jin-Seon ;
Yoon, Jeong Kyo .
MOLECULAR AND CELLULAR BIOLOGY, 2014, 34 (04) :752-764
[5]   A WNT/β-Catenin Signaling Activator, R-spondin, Plays Positive Regulatory Roles during Skeletal Myogenesis [J].
Han, Xiang Hua ;
Jin, Yong-Ri ;
Seto, Marianne ;
Yoon, Jeong Kyo .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (12) :10649-10659
[6]   Activation of the wnt signaling pathway: A molecular mechanism for lithium action [J].
Hedgepeth, CM ;
Conrad, LJ ;
Zhang, J ;
Huang, HC ;
Lee, VMY ;
Klein, PS .
DEVELOPMENTAL BIOLOGY, 1997, 185 (01) :82-91
[7]  
Huang J., 2013, P ANN M AM SOC BON M
[8]   Wnt/β-catenin/Tcf signaling induces the transcription of Axin2, a negative regulator of the signaling pathway [J].
Jho, EH ;
Zhang, T ;
Domon, C ;
Joo, CK ;
Freund, JN ;
Costantini, F .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (04) :1172-1183
[9]   β-catenin interacts with MyoD and regulates its transcription activity [J].
Kim, Chang-Hoon ;
Neiswender, Hannah ;
Baik, Eun Joo ;
Xiong, Wen C. ;
Mei, Lin .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (09) :2941-2951
[10]   A molecular mechanism for the effect of lithium on development [J].
Klein, PS ;
Melton, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) :8455-8459