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.
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18 October 1999
Article|
October 18 1999
The Receptor Tyrosine Phosphatase Crypα Promotes Intraretinal Axon Growth
Matthias M. Ledig,
Matthias M. Ledig
aMax-Planck-Institut für Entwicklungsbiologie, Physikalische Biologie, D-72076 Tübingen, Germany
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Fawaz Haj,
Fawaz Haj
bInstitute of Child Health, Neural Development Unit, University College London, London WC1N 1EH, United Kingdom
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John L. Bixby,
John L. Bixby
cDepartment of Molecular and Cellular Pharmacology and Neuroscience Program, University of Miami School of Medicine, Miami, Florida 33101
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Andrew W. Stoker,
Andrew W. Stoker
bInstitute of Child Health, Neural Development Unit, University College London, London WC1N 1EH, United Kingdom
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Bernhard K. Mueller
Bernhard K. Mueller
aMax-Planck-Institut für Entwicklungsbiologie, Physikalische Biologie, D-72076 Tübingen, Germany
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Matthias M. Ledig
aMax-Planck-Institut für Entwicklungsbiologie, Physikalische Biologie, D-72076 Tübingen, Germany
Fawaz Haj
bInstitute of Child Health, Neural Development Unit, University College London, London WC1N 1EH, United Kingdom
John L. Bixby
cDepartment of Molecular and Cellular Pharmacology and Neuroscience Program, University of Miami School of Medicine, Miami, Florida 33101
Andrew W. Stoker
bInstitute of Child Health, Neural Development Unit, University College London, London WC1N 1EH, United Kingdom
Bernhard K. Mueller
aMax-Planck-Institut für Entwicklungsbiologie, Physikalische Biologie, D-72076 Tübingen, Germany
1.used in this paper: AP, alkaline phosphatase; BM, basal membrane, BM-Ef, basal membranes with endfeet removed; ECM, extracellular matrix; LN, laminin; PLL, poly-l-lysine; RPTP, receptor protein tyrosine phosphatase
Dr. Haj's present address is Department of Surgery, Beth Israel Deaconess Medical Center and Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215.
Received:
April 30 1999
Revision Requested:
September 01 1999
Accepted:
September 01 1999
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 1999 The Rockefeller University Press
1999
The Rockefeller University Press
J Cell Biol (1999) 147 (2): 375–388.
Article history
Received:
April 30 1999
Revision Requested:
September 01 1999
Accepted:
September 01 1999
Citation
Matthias M. Ledig, Fawaz Haj, John L. Bixby, Andrew W. Stoker, Bernhard K. Mueller; The Receptor Tyrosine Phosphatase Crypα Promotes Intraretinal Axon Growth. J Cell Biol 18 October 1999; 147 (2): 375–388. doi: https://doi.org/10.1083/jcb.147.2.375
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