|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
First published online 19 April 2006
doi: 10.1242/dev.02365
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Department of Biological Regulation, Weizmann Institute of Science, Rehovot 76100, Israel.
* Author for correspondence (e-mail: eldad.tzahor{at}weizmann.ac.il)
Accepted 15 March 2006
During early embryogenesis, heart and skeletal muscle progenitor cells are thought to derive from distinct regions of the mesoderm (i.e. the lateral plate mesoderm and paraxial mesoderm, respectively). In the present study, we have employed both in vitro and in vivo experimental systems in the avian embryo to explore how mesoderm progenitors in the head differentiate into both heart and skeletal muscles. Using fate-mapping studies, gene expression analyses, and manipulation of signaling pathways in the chick embryo, we demonstrate that cells from the cranial paraxial mesoderm contribute to both myocardial and endocardial cell populations within the cardiac outflow tract. We further show that Bmp signaling affects the specification of mesoderm cells in the head: application of Bmp4, both in vitro and in vivo, induces cardiac differentiation in the cranial paraxial mesoderm and blocks the differentiation of skeletal muscle precursors in these cells. Our results demonstrate that cells within the cranial paraxial mesoderm play a vital role in cardiogenesis, as a new source of cardiac progenitors that populate the cardiac outflow tract in vivo. A deeper understanding of mesodermal lineage specification in the vertebrate head is expected to provide insights into the normal, as well as pathological, aspects of heart and craniofacial development.
Key words: Myogenesis, Secondary heart field, Cranial paraxial mesoderm, Splanchnic mesoderm, Bmp4
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
F. Rochais, K. Mesbah, and R. G. Kelly Signaling Pathways Controlling Second Heart Field Development Circ. Res., April 24, 2009; 104(8): 933 - 942. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Ferdous, A. Caprioli, M. Iacovino, C. M. Martin, J. Morris, J. A. Richardson, S. Latif, R. E. Hammer, R. P. Harvey, E. N. Olson, et al. Nkx2-5 transactivates the Ets-related protein 71 gene and specifies an endothelial/endocardial fate in the developing embryo PNAS, January 20, 2009; 106(3): 814 - 819. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Q. Teng, X. Zhao, J. P. Lees-Miller, F. R. Quinn, P. Li, D. E. Rancourt, B. London, J. C. Cross, and H. J. Duff Homozygous Missense N629D hERG (KCNH2) Potassium Channel Mutation Causes Developmental Defects in the Right Ventricle and Its Outflow Tract and Embryonic Lethality Circ. Res., December 5, 2008; 103(12): 1483 - 1491. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Nathan, A. Monovich, L. Tirosh-Finkel, Z. Harrelson, T. Rousso, A. Rinon, I. Harel, S. M. Evans, and E. Tzahor The contribution of Islet1-expressing splanchnic mesoderm cells to distinct branchiomeric muscles reveals significant heterogeneity in head muscle development Development, February 15, 2008; 135(4): 647 - 657. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Klaus, Y. Saga, M. M. Taketo, E. Tzahor, and W. Birchmeier Distinct roles of Wnt/beta-catenin and Bmp signaling during early cardiogenesis PNAS, November 20, 2007; 104(47): 18531 - 18536. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Rinon, S. Lazar, H. Marshall, S. Buchmann-Moller, A. Neufeld, H. Elhanany-Tamir, M. M. Taketo, L. Sommer, R. Krumlauf, and E. Tzahor Cranial neural crest cells regulate head muscle patterning and differentiation during vertebrate embryogenesis Development, September 1, 2007; 134(17): 3065 - 3075. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Dong, X. Sun, W. Liu, D. Ai, E. Klysik, M.-F. Lu, J. Hadley, L. Antoni, L. Chen, A. Baldini, et al. Pitx2 promotes development of splanchnic mesoderm-derived branchiomeric muscle Development, December 15, 2006; 133(24): 4891 - 4899. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Roberts, S. Ivins, A. C. Cook, A. Baldini, and P. J. Scambler Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick Hum. Mol. Genet., December 1, 2006; 15(23): 3394 - 3410. [Abstract] [Full Text] [PDF] |
||||