|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 120, Issue 8 2339-2346, Copyright © 1994 by Company of Biologists
JOURNAL ARTICLES |
K Symes, C Yordan and M Mercola
Department of Cell Biology, Harvard Medical School, Boston, MA 02115.
The involution of presumptive mesoderm that occurs during amphibian gastrulation is a complex process requiring the coordinated action of a diverse range of cells. We show that cells with distinct morphologies, resembling each of those normally found in the involuting tissue of the Xenopus embryo, are induced in dispersed animal pole cells by different doses of the potent mesoderm-inducing factor activin. Each cell type is induced within a restricted dose range of activin concentrations, the boundaries of which are well demarcated shortly after activin treatment. In contrast, Brachyury and goosecoid, two genes thought to pattern the presumptive mesoderm, and the gene encoding platelet-derived growth factor receptor alpha, which is expressed in the mesoderm of gastrula stage embryos, are induced by broad, overlapping ranges of high activin concentrations at such early times. Similarly, the response of the gene encoding platelet-derived growth factor A, which is expressed normally in ectoderm of gastrula stage embryos, diminishes gradually as the activin concentration increases. Dose windows for the expression of these four genes narrow and become distinct from one another in cell aggregates after several hours in culture, suggesting that activin prompts a dynamic program of gene expression in induced mesoderm.
This article has been cited by other articles:
![]() |
S. Tada, T. Era, C. Furusawa, H. Sakurai, S. Nishikawa, M. Kinoshita, K. Nakao, T. Chiba, and S.-I. Nishikawa Characterization of mesendoderm: a diverging point of the definitive endoderm and mesoderm in embryonic stem cell differentiation culture Development, October 1, 2005; 132(19): 4363 - 4374. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Ohkawara, K. Shirakabe, J. Hyodo-Miura, R. Matsuo, N. Ueno, K. Matsumoto, and H. Shibuya Role of the TAK1-NLK-STAT3 pathway in TGF-{beta}-mediated mesoderm induction Genes & Dev., February 15, 2004; 18(4): 381 - 386. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. M. Kwan and M. W. Kirschner Xbra functions as a switch between cell migration and convergent extension in the Xenopus gastrula Development, May 1, 2003; 130(9): 1961 - 1972. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. J. Dowd, C. L. Cooney, and M. A. Nugent Heparan Sulfate Mediates bFGF Transport through Basement Membrane by Diffusion with Rapid Reversible Binding J. Biol. Chem., February 19, 1999; 274(8): 5236 - 5244. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Gurdon, H Standley, S Dyson, K Butler, T Langon, K Ryan, F Stennard, K Shimizu, and A Zorn Single cells can sense their position in a morphogen gradient Development, January 12, 1999; 126(23): 5309 - 5317. [Abstract] [PDF] |
||||
![]() |
D. B. Constam and E. J. Robertson Regulation of Bone Morphogenetic Protein Activity by Pro Domains and Proprotein Convertases J. Cell Biol., January 11, 1999; 144(1): 139 - 149. [Abstract] [Full Text] [PDF] |
||||
![]() |
S Wacker, A Brodbeck, P Lemaire, C Niehrs, and R Winklbauer Patterns and control of cell motility in the Xenopus gastrula Development, January 5, 1998; 125(10): 1931 - 1942. [Abstract] [PDF] |
||||
![]() |
G. Conway, A. Margoliath, S. Wong-Madden, R. J. Roberts, and W. Gilbert Jak1 kinase is required for cell migrations and anterior specification in zebrafish embryos PNAS, April 1, 1997; 94(7): 3082 - 3087. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Armes and J. Smith The ALK-2 and ALK-4 activin receptors transduce distinct mesoderm-inducing signals during early Xenopus development but do not co-operate to establish thresholds Development, January 10, 1997; 124(19): 3797 - 3804. [Abstract] [PDF] |
||||
![]() |
C Chang, P. Wilson, L. Mathews, and A Hemmati-Brivanlou A Xenopus type I activin receptor mediates mesodermal but not neural specification during embryogenesis Development, January 2, 1997; 124(4): 827 - 837. [Abstract] [PDF] |
||||
![]() |
J C Baker and R M Harland A novel mesoderm inducer, Madr2, functions in the activin signal transduction pathway. Genes & Dev., August 1, 1996; 10(15): 1880 - 1889. [Abstract] [PDF] |
||||
![]() |
J. Ramos, C. Whittaker, and D. DeSimone Integrin-dependent adhesive activity is spatially controlled by inductive signals at gastrulation Development, January 9, 1996; 122(9): 2873 - 2883. [Abstract] [PDF] |
||||
![]() |
P Ataliotis, K Symes, M. Chou, L Ho, and M Mercola PDGF signalling is required for gastrulation of Xenopus laevis Development, January 9, 1995; 121(9): 3099 - 3110. [Abstract] [PDF] |
||||
![]() |
M. O'Reilly, J. Smith, and V Cunliffe Patterning of the mesoderm in Xenopus: dose-dependent and synergistic effects of Brachyury and Pintallavis Development, January 5, 1995; 121(5): 1351 - 1359. [Abstract] [PDF] |
||||
![]() |
D. Kessler and D. Melton Vertebrate embryonic induction: mesodermal and neural patterning Science, October 28, 1994; 266(5185): 596 - 604. [Abstract] [PDF] |
||||