|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 126, Issue 5 895-902, Copyright © 1999 by Company of Biologists
JOURNAL ARTICLES |
J Begbie, JF Brunet, JL Rubenstein and A Graham
Department of Experimental Pathology, GKT Medical School, Kings College London, Guys Campus, London SE1 9RT, UK.
The cranial sensory ganglia, in contrast to those of the trunk, have a dual embryonic origin arising from both neurogenic placodes and neural crest. Neurogenic placodes are focal thickenings of ectoderm, found exclusively in the head of vertebrate embryos. These structures can be split into two groups based on the positions that they occupy within the embryo, dorsolateral and epibranchial. The dorsolateral placodes develop alongside the central nervous system, while the epibranchial placodes are located close to the top of the clefts between the branchial arches. Importantly, previous studies have shown that the neurogenic placodes form under the influence of the surrounding cranial tissues. In this paper, we have analysed the nature of the inductive signal underlying the formation of the epibranchial placodes. We find that epibranchial placodes do not require neural crest for their induction, but rather that it is the pharyngeal endoderm that is the source of the inductive signal. We also find that, while cranial ectoderm is competent to respond to this inductive signal, trunk ectoderm is not. We have further identified the signalling molecule Bmp7 as the mediator of this inductive interaction. This molecule is expressed in a manner consistent with it playing such a role and, when added to ectoderm explants, it will promote the formation of epibranchial neuronal cells. Moreover, the Bmp7 antagonist follstatin will block the ability of pharyngeal endoderm to induce placodal neuronal cells, demonstrating that Bmp7 is required for this inductive interaction. This work answers the long standing question regarding the induction of the epibranchial placodes, and represents the first elucidation of an inductive mechanism, and a molecular effector, underlying the formation of any primary sensory neurons in higher vertebrates.
This article has been cited by other articles:
![]() |
S. Freter, Y. Muta, S.-S. Mak, S. Rinkwitz, and R. K. Ladher Progressive restriction of otic fate: the role of FGF and Wnt in resolving inner ear potential Development, October 15, 2008; 135(20): 3415 - 3424. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. G. Northcutt Historical hypotheses regarding segmentation of the vertebrate head Integr. Comp. Biol., June 28, 2008; (2008) icn065v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. L. McCabe and M. Bronner-Fraser Essential role for PDGF signaling in ophthalmic trigeminal placode induction Development, May 15, 2008; 135(10): 1863 - 1874. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Kuratani Is the vertebrate head segmented?--evolutionary and developmental considerations Integr. Comp. Biol., April 17, 2008; (2008) icn015v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Graham, A. Blentic, S. Duque, and J. Begbie Delamination of cells from neurogenic placodes does not involve an epithelial-to-mesenchymal transition Development, December 1, 2007; 134(23): 4141 - 4145. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Chambers, L. Wilson, M. Maden, and A. Lumsden RALDH-independent generation of retinoic acid during vertebrate embryogenesis by CYP1B1 Development, April 1, 2007; 134(7): 1369 - 1383. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Nechiporuk, T. Linbo, K. D. Poss, and D. W. Raible Specification of epibranchial placodes in zebrafish Development, February 1, 2007; 134(3): 611 - 623. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. von Scheven, L. E. Alvares, R. C. Mootoosamy, and S. Dietrich Neural tube derived signals and Fgf8 act antagonistically to specify eye versus mandibular arch muscles Development, July 15, 2006; 133(14): 2731 - 2745. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Martin and A. K. Groves Competence of cranial ectoderm to respond to Fgf signaling suggests a two-step model of otic placode induction Development, March 1, 2006; 133(5): 877 - 887. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Ohyama, O. A. Mohamed, M. M. Taketo, D. Dufort, and A. K. Groves Wnt signals mediate a fate decision between otic placode and epidermis Development, March 1, 2006; 133(5): 865 - 875. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Litsiou, S. Hanson, and A. Streit A balance of FGF, BMP and WNT signalling positions the future placode territory in the head Development, September 15, 2005; 132(18): 4051 - 4062. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Nechiporuk, T. Linbo, and D. W. Raible Endoderm-derived Fgf3 is necessary and sufficient for inducing neurogenesis in the epibranchial placodes in zebrafish Development, August 15, 2005; 132(16): 3717 - 3730. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Holzschuh, N. Wada, C. Wada, A. Schaffer, Y. Javidan, A. Tallafuss, L. Bally-Cuif, and T. F. Schilling Requirements for endoderm and BMP signaling in sensory neurogenesis in zebrafish Development, August 15, 2005; 132(16): 3731 - 3742. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. K. Ladher, T. J. Wright, A. M. Moon, S. L. Mansour, and G. C. Schoenwolf FGF8 initiates inner ear induction in chick and mouse Genes & Dev., March 1, 2005; 19(5): 603 - 613. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Zou, D. Silvius, B. Fritzsch, and P.-X. Xu Eya1 and Six1 are essential for early steps of sensory neurogenesis in mammalian cranial placodes Development, November 15, 2004; 131(22): 5561 - 5572. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Quinlan, P. Martin, and A. Graham The role of actin cables in directing the morphogenesis of the pharyngeal pouches Development, February 1, 2004; 131(3): 593 - 599. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Holzschuh, A. Barrallo-Gimeno, A.-K. Ettl, K. Durr, E. W. Knapik, and W. Driever Noradrenergic neurons in the zebrafish hindbrain are induced by retinoic acid and require tfap2a for expression of the neurotransmitter phenotype Development, December 1, 2003; 130(23): 5741 - 5754. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Bachiller, J. Klingensmith, N. Shneyder, U. Tran, R. Anderson, J. Rossant, and E. M. De Robertis The role of chordin/Bmp signals in mammalian pharyngeal development and DiGeorge syndrome Development, August 1, 2003; 130(15): 3567 - 3578. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. A. Lee, E. L. Shen, A. Fiser, A. Sali, and S. Guo The zebrafish forkhead transcription factor Foxi1 specifies epibranchial placode-derived sensory neurons Development, June 15, 2003; 130(12): 2669 - 2679. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Matt, N. B. Ghyselinck, O. Wendling, P. Chambon, and M. Mark Retinoic acid-induced developmental defects are mediated by RAR{beta}/RXR heterodimers in the pharyngeal endoderm Development, May 15, 2003; 130(10): 2083 - 2093. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Grigaliunas, R. M. Bradley, D. K. MacCallum, and C. M. Mistretta Distinctive Neurophysiological Properties of Embryonic Trigeminal and Geniculate Neurons in Culture J Neurophysiol, October 1, 2002; 88(4): 2058 - 2074. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Begbie and A. Graham Integration Between the Epibranchial Placodes and the Hindbrain Science, October 19, 2001; 294(5542): 595 - 598. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Gavalas, P. Trainor, L. Ariza-McNaughton, and R. Krumlauf Synergy between Hoxa1 and Hoxb1: the relationship between arch patterning and the generation of cranial neural crest Development, August 1, 2001; 128(15): 3017 - 3027. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. M. Shimeld and P. W. H. Holland Special Feature: Vertebrate innovations PNAS, April 25, 2000; 97(9): 4449 - 4452. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Baker and M Bronner-Fraser Establishing neuronal identity in vertebrate neurogenic placodes Development, January 7, 2000; 127(14): 3045 - 3056. [Abstract] [PDF] |
||||
![]() |
O Wendling, C Dennefeld, P Chambon, and M Mark Retinoid signaling is essential for patterning the endoderm of the third and fourth pharyngeal arches Development, January 4, 2000; 127(8): 1553 - 1562. [Abstract] [PDF] |
||||
![]() |
M. Depew, J. Liu, J. Long, R Presley, J. Meneses, R. Pedersen, and J. Rubenstein Dlx5 regulates regional development of the branchial arches and sensory capsules Development, January 9, 1999; 126(17): 3831 - 3846. [Abstract] [PDF] |
||||