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The receptor tyrosine phosphatase CRYPalpha promotes intraretinal axon growth

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Ledig,  MM
Department Physical Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Mueller,  BK       
Department Physical Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Citation

Ledig, M., Haj, J., Bixby, F., Stoker, A., & Mueller, B. (1999). The receptor tyrosine phosphatase CRYPalpha promotes intraretinal axon growth. The Journal of Cell Biology, 147(2), 375-388. doi:10.1083/jcb.147.2.375.


Cite as: https://hdl.handle.net/21.11116/0000-000B-9CC1-B
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 CRYPalpha 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 CRYPalpha 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 CRYPalpha 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 CRYPalpha 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.