Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
???displayArticle.abstract??? Mesoderm formation is a result of cell-cell interactions between the vegetal and animal hemisphere and is thought to be mediated by inducing peptide growth factors including members of the FGF and TGFβ superfamilies. Our immunochemical study analyses the distribution of FGF receptors coded by the human flg gene during embryogenesis of Xenopus laevis. Immunostaining was detected in the dorsal and ventralectoderm and also in the marginal zone of early cleavage, blastula and gastrula stages. Signals were very strong in the mid and late blastula (stage 8 and 9) and declined slightly in the early gastrula (stage 10). A dramatic decrease was observed up to the late gastrula (stage 11+). In stage 13 embryos, immunostaining was only found in cells around the blastopore. Isolated ectoderm cultured in vitro showed a similar temporal expression and decrease of the signal as the normal embryos. These results indicate that receptor expression is independent of the interaction of the animal cells with the vegetal part of the embryo. Of interest is the fact that the signal cannot only be found at or near the cell surface but also within the cell. This suggests the presence of an intracellular isoform of the receptor resulting from the endogenous expression of splice variants and the internalization of transmembrane receptor. Taken together our results suggest that the loss of competence (for bFGF around stage 10) is not directly correlated with the presence of receptors. The possible roles of heparan sulphate glucosaminoglycans (low affinity receptors) and control mechanisms in the intracellular signalling pathway downstream of the receptor level should be taken into consideration.
Amaya,
Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos.
1991, Pubmed,
Xenbase
Amaya,
Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos.
1991,
Pubmed
,
Xenbase
Asashima,
Inducing effects of the presumptive endoderm of successive stages inTriturus alpestris.
1975,
Pubmed
Coughlin,
Acidic and basic fibroblast growth factors stimulate tyrosine kinase activity in vivo.
1988,
Pubmed
Dale,
Mesoderm induction in Xenopus laevis: a quantitative study using a cell lineage label and tissue-specific antibodies.
1985,
Pubmed
,
Xenbase
Friesel,
cDNA cloning and developmental expression of fibroblast growth factor receptors from Xenopus laevis.
1991,
Pubmed
,
Xenbase
Gillespie,
Analysis of competence: receptors for fibroblast growth factor in early Xenopus embryos.
1989,
Pubmed
,
Xenbase
Godsave,
Mesoderm-inducing factors: a small class of molecules.
1988,
Pubmed
,
Xenbase
Grunz,
The inducing capacity of the presumptive endoderm of Xenopus laevis studied by transfilter experiments.
1986,
Pubmed
,
Xenbase
Grunz,
Extracellular matrix components prevent neural differentiation of disaggregated Xenopus ectoderm cells.
1990,
Pubmed
,
Xenbase
Grunz,
Neural differentiation of Xenopus laevis ectoderm takes place after disaggregation and delayed reaggregation without inducer.
1989,
Pubmed
,
Xenbase
Grunz,
[Relationship between competence and protein synthesis in amphibian ectoderm].
1970,
Pubmed
Grunz,
Induction of mesodermal tissues by acidic and basic heparin binding growth factors.
1988,
Pubmed
,
Xenbase
Grunz,
[Experimental studies on competence in early development of amphibian ectoderm].
1968,
Pubmed
Grunz,
The differentiation of isolated amphibian ectoderm with or without treatment with an inductor : A scanning electron microscop study.
1975,
Pubmed
Grunz,
Change in the differentiation pattern ofXenopus laevis ectoderm by variation of the incubation time and concentration of vegetalizing factor.
1983,
Pubmed
,
Xenbase
Hou,
Fibroblast growth factor receptors from liver vary in three structural domains.
1991,
Pubmed
Kan,
Receptor phenotype underlies differential response of hepatocytes and nonparenchymal cells to heparin-binding fibroblast growth factor type 1 (aFGF) and type 2 (bFGF).
1992,
Pubmed
Kimelman,
Synergistic induction of mesoderm by FGF and TGF-beta and the identification of an mRNA coding for FGF in the early Xenopus embryo.
1987,
Pubmed
,
Xenbase
Kimelman,
The presence of fibroblast growth factor in the frog egg: its role as a natural mesoderm inducer.
1988,
Pubmed
,
Xenbase
Kirschner,
A new method of local vital staining of amphibian embryos using ficoll and "crystals" of Nile Red.
1980,
Pubmed
Klagsbrun,
A dual receptor system is required for basic fibroblast growth factor activity.
1991,
Pubmed
Knöchel,
Mesoderm-inducing factors. Their possible relationship to heparin-binding growth factors and transforming growth factor-beta.
1987,
Pubmed
Musci,
Regulation of the fibroblast growth factor receptor in early Xenopus embryos.
1990,
Pubmed
,
Xenbase
Nieuwkoop,
The formation of the mesoderm in urodelean amphibians : I. Induction by the endoderm.
1969,
Pubmed
Nieuwkoop,
The organization center of the amphibian embryo: its origin, spatial organization, and morphogenetic action.
1973,
Pubmed
Orr-Urtreger,
Developmental expression of two murine fibroblast growth factor receptors, flg and bek.
1991,
Pubmed
Rosa,
Mesoderm induction in amphibians: the role of TGF-beta 2-like factors.
1988,
Pubmed
,
Xenbase
Shi,
16-kilodalton heparin binding (fibroblast) growth factor type one appears in a stable 40-kilodalton complex after receptor-dependent internalization.
1991,
Pubmed
Shiurba,
Nuclear translocation of fibroblast growth factor during Xenopus mesoderm induction.
1991,
Pubmed
,
Xenbase
Slack,
Mesoderm induction in early Xenopus embryos by heparin-binding growth factors.
,
Pubmed
,
Xenbase
Slack,
Inductive effects of fibroblast growth factor and lithium ion on Xenopus blastula ectoderm.
1988,
Pubmed
,
Xenbase
Yan,
Expression and transforming activity of a variant of the heparin-binding fibroblast growth factor receptor (flg) gene resulting from splicing of the alpha exon at an alternate 3'-acceptor site.
1992,
Pubmed