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  The receptor tyrosine phosphatase CRYPalpha promotes intraretinal axon growth

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.

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 Creators:
Ledig, MM1, Author           
Haj, J, Author
Bixby, FL, Author
Stoker, AW, Author
Mueller, BK1, Author                 
Affiliations:
1Department Physical Biology, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3384683              

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 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.

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 Dates: 1999-10
 Publication Status: Issued
 Pages: -
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 Rev. Type: -
 Identifiers: DOI: 10.1083/jcb.147.2.375
PMID: 10525542
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Title: The Journal of Cell Biology
  Other : JBC
Source Genre: Journal
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Publ. Info: New York, NY : Rockefeller Institute Press
Pages: - Volume / Issue: 147 (2) Sequence Number: - Start / End Page: 375 - 388 Identifier: ISSN: 0021-9525
CoNE: https://pure.mpg.de/cone/journals/resource/991042742946024_2