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PLoS Biol. 2014 Sep 23;12(9):e1001955. doi: 10.1371/journal.pbio.1001955. eCollection 2014 Sep.

Variable combinations of specific ephrin ligand/Eph receptor pairs control embryonic tissue separation.

Author information

1
Department of Biology, McGill University, Montreal, Quebec, Canada.
2
Complex Systems and Non Linear Phenomena, L2C-UMR 5221 CNRS-UM2, Montpellier, France; Biological Physics and Systems Biology, DIMNP-UMR 5235 CNRS-UM2 et 1, Montpellier, France.
3
Department of Cell and Systems Biology, University of Toronto, Toronto, Canada.

Abstract

Ephrins and Eph receptors are involved in the establishment of vertebrate tissue boundaries. The complexity of the system is puzzling, however in many instances, tissues express multiple ephrins and Ephs on both sides of the boundary, a situation that should in principle cause repulsion between cells within each tissue. Although co-expression of ephrins and Eph receptors is widespread in embryonic tissues, neurons, and cancer cells, it is still unresolved how the respective signals are integrated into a coherent output. We present a simple explanation for the confinement of repulsion to the tissue interface: Using the dorsal ectoderm-mesoderm boundary of the Xenopus embryo as a model, we identify selective functional interactions between ephrin-Eph pairs that are expressed in partial complementary patterns. The combined repulsive signals add up to be strongest across the boundary, where they reach sufficient intensity to trigger cell detachments. The process can be largely explained using a simple model based exclusively on relative ephrin and Eph concentrations and binding affinities. We generalize these findings for the ventral ectoderm-mesoderm boundary and the notochord boundary, both of which appear to function on the same principles. These results provide a paradigm for how developmental systems may integrate multiple cues to generate discrete local outcomes.

PMID:
25247423
PMCID:
PMC4172438
DOI:
10.1371/journal.pbio.1001955
[Indexed for MEDLINE]
Free PMC Article

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