|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 119, Issue 4 1067-1078, Copyright © 1993 by Company of Biologists
JOURNAL ARTICLES |
M Kengaku and H Okamoto
Department of Neurobiology, Faculty of Medicine, University of Tokyo, Japan.
The vertebrate nervous system is initially induced from a section of dorsal ectoderm by signal(s) from the underlying dorsal mesoderm during gastrulation. In an effort to identify the neural inducing factor(s) emanating from the dorsal mesoderm, we have examined the inductive action of various growth factors by applying them to ectoderm cells from Xenopus gastrulae (8- to 12.5-hour age; embryonic stage 9+ to 11 1/2) in a microculture system. Monoclonal antibodies that specifically recognize cellular differentiation antigens from three distinct ectoderm lineages (N1 for CNS neurons from neural tube, Me1 for melanophores from neural crest and E3 for skin epidermal cells from epidermal lineages, respectively) and a mesoderm lineage (Mu1 for muscle cells) were used as markers to monitor the differentiation of cultured ectoderm cells. We found that basic fibroblast growth factor (bFGF) was capable of specifically and reproducibly inducing gastrula ectoderm cells to produce CNS neurons and melanophores at concentrations as low as 5 pM, a value about 50-fold lower than that required to induce the formation of muscle cells from blastula animal cap cells (6-hour age; stage 8+). The induction of neural lineages by bFGF was correlated with a suppression of epidermal differentiation in a dose-dependent manner. bFGF never induced the formation of muscle cells from gastrula ectoderm cells even at concentrations as high as 5 nM. The response of ectoderm cells to bFGF changed dramatically during gastrulation. Ectoderm cells from early (8- to 9-hour age; stage 9+ to 10) gastrula gave rise to CNS neurons, but yielded few melanophores. As ectoderm cells were prepared from gastrulae of increasing age, their competence to form neurons was gradually lost, whereas the production of melanophores was enhanced and peaked in 11-hour gastrula (stage 10 1/2). The ability to form both neurons and melanophores was substantially reduced in 12.5-hour gastrula (stage 11 1/2). By examining ectoderm cells from the ventral and dorsal sides independently, it was also shown that during gastrulation the change in response to bFGF of the ventral ectoderm preceded that of the dorsal ectoderm. The state of competence of the ectoderm changed primarily due to intrinsic factors rather than by instruction from other parts of the gastrula embryo. This was shown by adding bFGF to cultures of ectoderm cells that were isolated at 9-hour (stage 10) and cultured for increasing periods to allow their autonomous development. The time course of both loss of neuronal competence and gain and loss of melanophore competence closely paralleled that observed in vivo during gastrulation.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
C.-S. Hong, B.-Y. Park, and J.-P. Saint-Jeannet Fgf8a induces neural crest indirectly through the activation of Wnt8 in the paraxial mesoderm Development, December 1, 2008; 135(23): 3903 - 3910. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Gaulden and J. F. Reiter Neur-ons and neur-offs: regulators of neural induction in vertebrate embryos and embryonic stem cells Hum. Mol. Genet., April 15, 2008; 17(R1): R60 - R66. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Chang and R. M. Harland Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation Development, November 1, 2007; 134(21): 3861 - 3872. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Massague Integration of Smad and MAPK pathways: a link and a linker revisited Genes & Dev., December 15, 2003; 17(24): 2993 - 2997. [Full Text] [PDF] |
||||
![]() |
T. Haremaki, Y. Tanaka, I. Hongo, M. Yuge, and H. Okamoto Integration of multiple signal transducing pathways on Fgf response elements of the Xenopus caudal homologue Xcad3 Development, October 15, 2003; 130(20): 4907 - 4917. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Zhang, H. M. El-Hodiri, H.-F. Ma, X. Zhang, M. Servetnick, T. G. Wensel, and M. Jamrich Targeted expression of the dominant-negative FGFR4a in the eye using Xrx1A regulatory sequences interferes with normal retinal development Development, September 1, 2003; 130(17): 4177 - 4186. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-I. Yabe, K. Tanegashima, Y. Haramoto, S. Takahashi, T. Fujii, S. Kozuma, Y. Taketani, and M. Asashima FRL-1, a member of the EGF-CFC family, is essential for neural differentiation in Xenopus early development Development, May 15, 2003; 130(10): 2071 - 2081. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Dono Fibroblast growth factors as regulators of central nervous system development and function Am J Physiol Regulatory Integrative Comp Physiol, April 1, 2003; 284(4): R867 - R881. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Kudoh, S. W. Wilson, and I. B. Dawid Distinct roles for Fgf, Wnt and retinoic acid in posteriorizing the neural ectoderm Development, March 11, 2003; 129(18): 4335 - 4346. [Abstract] [Full Text] [PDF] |
||||
![]() |
M Carl and J Wittbrodt Graded interference with FGF signalling reveals its dorsoventral asymmetry at the mid-hindbrain boundary Development, January 12, 1999; 126(24): 5659 - 5667. [Abstract] [PDF] |
||||
![]() |
A. R. Uzgare, J. A. Uzman, H. M. El-Hodiri, and A. K. Sater Mitogen-activated protein kinase and neural specification in Xenopus PNAS, December 8, 1998; 95(25): 14833 - 14838. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. TAKAHASHI and Y. OKAMURA Ion Channels and Early Development of Neural Cells Physiol Rev, April 1, 1998; 78(2): 307 - 337. [Abstract] [Full Text] [PDF] |
||||
![]() |
C LaBonne and M Bronner-Fraser Neural crest induction in Xenopus: evidence for a two-signal model Development, January 7, 1998; 125(13): 2403 - 2414. [Abstract] [PDF] |
||||
![]() |
S Koshida, M Shinya, T Mizuno, A Kuroiwa, and H Takeda Initial anteroposterior pattern of the zebrafish central nervous system is determined by differential competence of the epiblast Development, January 5, 1998; 125(10): 1957 - 1966. [Abstract] [PDF] |
||||
![]() |
K. Storey, A Goriely, C. Sargent, J. Brown, H. Burns, H. Abud, and J. Heath Early posterior neural tissue is induced by FGF in the chick embryo Development, January 2, 1998; 125(3): 473 - 484. [Abstract] [PDF] |
||||
![]() |
K Mizuseki, M Kishi, M Matsui, S Nakanishi, and Y Sasai Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction Development, January 2, 1998; 125(4): 579 - 587. [Abstract] [PDF] |
||||
![]() |
R.-H. Xu, J. Kim, M. Taira, D. Sredni, and H.-f. Kung Studies on the Role of Fibroblast Growth Factor Signaling in Neurogenesis Using Conjugated/Aged Animal Caps and Dorsal Ectoderm-Grafted Embryos J. Neurosci., September 15, 1997; 17(18): 6892 - 6898. [Abstract] [Full Text] [PDF] |
||||
![]() |
D Henrique, D Tyler, C Kintner, J K Heath, J H Lewis, D Ish-Horowicz, and K G Storey cash4, a novel achaete-scute homolog induced by Hensen's node during generation of the posterior nervous system. Genes & Dev., March 1, 1997; 11(5): 603 - 615. [Abstract] [PDF] |
||||
![]() |
M. Taira, J.-P. Saint-Jeannet, and I. B. Dawid Role of the Xlim-1 and Xbra genes in anteroposterior patterning of neural tissue by the head and trunk organizer PNAS, February 4, 1997; 94(3): 895 - 900. [Abstract] [Full Text] [PDF] |
||||
![]() |
R Morgan and M. Sargent The role in neural patterning of translation initiation factor eIF4AII; induction of neural fold genes Development, January 7, 1997; 124(14): 2751 - 2760. [Abstract] [PDF] |
||||
![]() |
C. Hansen, C. Marion, K Steele, S George, and W. Smith Direct neural induction and selective inhibition of mesoderm and epidermis inducers by Xnr3 Development, January 1, 1997; 124(2): 483 - 492. [Abstract] [PDF] |
||||
![]() |
K. Kroll and E Amaya Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation Development, January 10, 1996; 122(10): 3173 - 3183. [Abstract] [PDF] |
||||
![]() |
C Launay, V Fromentoux, D. Shi, and J. Boucaut A truncated FGF receptor blocks neural induction by endogenous Xenopus inducers Development, January 3, 1996; 122(3): 869 - 880. [Abstract] [PDF] |
||||
![]() |
T. Lamb and R. Harland Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior neural pattern Development, January 11, 1995; 121(11): 3627 - 3636. [Abstract] [PDF] |
||||
![]() |
M Kengaku and H Okamoto bFGF as a possible morphogen for the anteroposterior axis of the central nervous system in Xenopus Development, January 9, 1995; 121(9): 3121 - 3130. [Abstract] [PDF] |
||||
![]() |
C. Lai, S. Ekker, P. Beachy, and R. Moon Patterning of the neural ectoderm of Xenopus laevis by the amino-terminal product of hedgehog autoproteolytic cleavage Development, January 8, 1995; 121(8): 2349 - 2360. [Abstract] [PDF] |
||||
![]() |
A. Knecht, P. Good, I. Dawid, and R. Harland Dorsal-ventral patterning and differentiation of noggin-induced neural tissue in the absence of mesoderm Development, January 6, 1995; 121(6): 1927 - 1935. [Abstract] [PDF] |
||||
![]() |
R Mayor, R Morgan, and M. Sargent Induction of the prospective neural crest of Xenopus Development, January 3, 1995; 121(3): 767 - 777. [Abstract] [PDF] |
||||
![]() |
S. Pruitt Discrete endogenous signals mediate neural competence and induction in P19 embryonal carcinoma stem cells Development, January 11, 1994; 120(11): 3301 - 3312. [Abstract] [PDF] |
||||