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PMID: 7555734 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

PDGF signalling is required for gastrulation of Xenopus laevis.

Development (Cambridge, England) ·Vol. 121 ·No. 9 ·1995-09-00 ·Pages 3099-110

Ataliotis P, Symes K, Chou MM, Ho L, Mercola M

Abstract

During Xenopus gastrulation, platelet-derived growth factor (PDGF) receptor-alpha is expressed in involuting marginal zone cells which migrate over ectodermal cells expressing PDGF-A. To investigate the role of PDGF signalling during this process, we have generated a novel point mutant of PDGF receptor-alpha analogous to the W37 mutation of c-kit. This molecule is a specific, potent, dominant inhibitor of PDGF signalling in vivo. Injection of RNA encoding this protein into Xenopus embryos prevents closure of the blastopore, leads to abnormal gastrulation and a loss of anterior structures. Convergent extension is not inhibited in these embryos, but rather, involuting mesodermal cells fail to adhere to the overlying ectoderm. PDGF may therefore be required for mesodermal cell-substratum interaction.

MeSH Terms
Animals Gastrula/physiology,ultrastructure In Situ Hybridization Mesoderm/physiology Morphogenesis/physiology Mutagenesis, Site-Directed Platelet-Derived Growth Factor/physiology Polymerase Chain Reaction Receptors, Platelet-Derived Growth Factor Signal Transduction/physiology Xenopus laevis/embryology
Chemicals
Platelet-Derived Growth Factor Receptors, Platelet-Derived Growth Factor
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ataliotis P
Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Symes K
Chou M M
Ho L
Mercola M
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1995-09-00
Pages
3099-110
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NICHD NIH HHS · 1HF32HD07561 · United States
NICHD NIH HHS · R01 HD28460 · United States
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