TY - JOUR
T1 - Antagonistic crosstalk of Wnt/β-catenin/Bmp signaling within the Apical Ectodermal Ridge (AER) regulates interdigit formation
AU - Villacorte, Mylah
AU - Suzuki, Kentaro
AU - Hayashi, Katsuhiko
AU - de Sousa Lopes, Susana Chuva
AU - Haraguchi, Ryuma
AU - Taketo, Makoto M.
AU - Nakagata, Naomi
AU - Yamada, Gen
N1 - Funding Information:
We thank Drs. R. Zeller, R. Behringer, M. Lewandoski, Y. Mishina, B. Crenshaw, W. Birchmeier, A. McMahon, P. Chambon, T. Yamaguchi, A. Moon, J. Takeda, C. Takada, S. Fujikawa, and S. Miyaji for materials and helps. This work was supported by Grant-in-Aid for Scientific Research B, Scientific Research on Priority Areas (General promotion of Cancer research in Japan), and the Global COE program Cell Fate Regulation Research and Education Unit from the Ministry of Education, Culture, Sports, Science, and Technology, Japan , and a grant for Child Health and Development (17-2, 20-3) and Health Sciences Research Grant from the Ministry of Health, Labor, and Welfare, Japan . This work was also supported by National Institutes of Health Grant R01-ES016597-01A1 .
PY - 2010/1/22
Y1 - 2010/1/22
N2 - Digit and interdigit (D/ID) development is one of the important research fields in molecular developmental biology. Interdigital cell death (ICD) is a morphogenetic event which has been considered as an essential process for D/ID formation. Although some growth factors including Bmp and Fgf signaling can modulate ICD, growth factor crosstalk regulating ICD is poorly understood. Wnt canonical pathway and Bmp signal crosstalk has been considered as the essential growth factor crosstalk in organogenesis. To elucidate the crosstalk to regulate the D/ID formation, we analyzed conditional mutant mice with limb bud ectoderm expressing constitutively activated β-catenin signaling. We showed that modulation of Wnt/β-catenin signal in the limb ectoderm including the AER regulates ID apoptosis. We also demonstrated that Wnt/β-catenin signaling in the ectoderm can positively regulate Fgf8 possibly antagonizing the epithelial derived Bmp signaling. Human birth defects for digit abnormalities have been known to be affected by multiple parameters. Elucidation of the potential mechanisms underlying such D/ID development is an urgent medical issue to be solved. This work would be one of the first studies showing essential growth factor cascades in the D/ID formation.
AB - Digit and interdigit (D/ID) development is one of the important research fields in molecular developmental biology. Interdigital cell death (ICD) is a morphogenetic event which has been considered as an essential process for D/ID formation. Although some growth factors including Bmp and Fgf signaling can modulate ICD, growth factor crosstalk regulating ICD is poorly understood. Wnt canonical pathway and Bmp signal crosstalk has been considered as the essential growth factor crosstalk in organogenesis. To elucidate the crosstalk to regulate the D/ID formation, we analyzed conditional mutant mice with limb bud ectoderm expressing constitutively activated β-catenin signaling. We showed that modulation of Wnt/β-catenin signal in the limb ectoderm including the AER regulates ID apoptosis. We also demonstrated that Wnt/β-catenin signaling in the ectoderm can positively regulate Fgf8 possibly antagonizing the epithelial derived Bmp signaling. Human birth defects for digit abnormalities have been known to be affected by multiple parameters. Elucidation of the potential mechanisms underlying such D/ID development is an urgent medical issue to be solved. This work would be one of the first studies showing essential growth factor cascades in the D/ID formation.
UR - http://www.scopus.com/inward/record.url?scp=74449086905&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=74449086905&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2009.12.109
DO - 10.1016/j.bbrc.2009.12.109
M3 - Article
C2 - 20043884
AN - SCOPUS:74449086905
VL - 391
SP - 1653
EP - 1657
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
SN - 0006-291X
IS - 4
ER -