The Receptor Tyrosine Phosphatase Crypα Promotes Intraretinal Axon Growth

Author:

Ledig Matthias M.1,Haj Fawaz2,Bixby John L.3,Stoker Andrew W.2,Mueller Bernhard K.1

Affiliation:

1. Max-Planck-Institut für Entwicklungsbiologie, Physikalische Biologie, D-72076 Tübingen, Germany

2. Institute of Child Health, Neural Development Unit, University College London, London WC1N 1EH, United Kingdom

3. Department of Molecular and Cellular Pharmacology and Neuroscience Program, University of Miami School of Medicine, Miami, Florida 33101

Abstract

Retinal ganglion cell axons grow towards the optic fissure in close contact with the basal membrane, an excellent growth substratum. One of the ligands of receptor tyrosine phosphatase CRYPα is located on the retinal and tectal basal membranes. To analyze the role of this RPTP and its ligand in intraretinal growth and guidance of ganglion cell axons, we disrupted ligand- receptor interactions on the retinal basal membrane in culture. Antibodies against CRYPα strongly reduced retinal axon growth on the basal membrane, and induced a dramatic change in morphology of retinal growth cones, reducing the size of growth cone lamellipodia. A similar effect was observed by blocking the ligand with a CRYPα ectodomain fusion protein. These effects did not occur, or were much reduced, when axons were grown either on laminin-1, on matrigel or on basal membranes with glial endfeet removed. This indicates that a ligand for CRYPα is located on glial endfeet. These results show for the first time in vertebrates that the interaction of a receptor tyrosine phosphatase with its ligand is crucial not only for promotion of retinal axon growth but also for maintenance of retinal growth cone lamellipodia on basal membranes.

Publisher

Rockefeller University Press

Subject

Cell Biology

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