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  The receptor tyrosine phosphatase CRYPalpha affects growth cone morphology

Mueller, B., Ledig, M., & Wahl, S. (2000). The receptor tyrosine phosphatase CRYPalpha affects growth cone morphology. Journal of Neurobiology, 44(2), 204-218.

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 Urheber:
Mueller, BK1, Autor                 
Ledig, MM1, Autor           
Wahl, S1, Autor           
Affiliations:
1Department Physical Biology, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3384683              

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 Zusammenfassung: During development of the nervous system receptor tyrosine kinases and receptor protein tyrosine phosphatases act in a coordinate way during axon growth and guidance. In the developing avian retinotectal system, many different receptor protein tyrosine phosphatases are expressed. Most of them have unknown functions. Retinal ganglion cells express at least three different members of this receptor family on their axons and growth cones: CRYPalpha, CRYP-2 and PTPmu. CRYPalpha interacts heterophilically with at least two different ligands found in the basal membranes of the retina and the optic tectum. To analyze the role of the CRYPalpha-ligand interaction, retinal ganglion cell axons were grown on retinal basal membranes (inner limiting membrane) and the receptor-ligand interaction was blocked from both the receptor side (by receptor specific antibodies) and from the ligand side by using a receptor-alkaline phosphatase fusion protein. Both of these treatments reduced average retinal axon length and induced a dramatic change in morphology of retinal ganglion cell growth cones on basal membranes, but not on other substrates like laminin, N-cadherin, matrigel- and detergent-treated basal membranes. These results suggest that CRYPalpha and its ligand act as growth-promoting molecules during intraretinal axon growth.

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 Datum: 2000-08
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Identifikatoren: PMID: 10934323
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Titel: Journal of Neurobiology
  Andere : J. Neurobiol.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: New York : Wiley-Interscience.
Seiten: - Band / Heft: 44 (2) Artikelnummer: - Start- / Endseite: 204 - 218 Identifikator: ISSN: 0022-3034
CoNE: https://pure.mpg.de/cone/journals/resource/1000000000256970