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Extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins

We have developed an in vitro assay which measures the ability of growth cones to extend on an axonal substrate. Neurite lengths were compared in the presence or absence of monovalent antibodies against specific neural cell surface glycoproteins. Fab fragments of antibodies against the neural cell a...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1987
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114414/
https://www.ncbi.nlm.nih.gov/pubmed/3543026
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description We have developed an in vitro assay which measures the ability of growth cones to extend on an axonal substrate. Neurite lengths were compared in the presence or absence of monovalent antibodies against specific neural cell surface glycoproteins. Fab fragments of antibodies against the neural cell adhesion molecule, NCAM, have an insignificant effect on the lengths of neurites elongating on either an axonal substrate or a laminin substrate. Fab fragments of polyclonal antibodies against two new neural cell surface antigens, defined by mAb G4 and mAb F11, decrease the lengths of neurites elongating on an axonal substrate, but have no effect on the lengths of neurites elongating on a laminin substrate. G4 antigen is related to mouse L1, while F11 antigen appears to be distinct from all known neural cell surface glycoproteins. Our results suggest that the G4 and F11 antigens help to promote the extension of growth cones on axons.
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spelling pubmed-21144142008-05-01 Extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins J Cell Biol Articles We have developed an in vitro assay which measures the ability of growth cones to extend on an axonal substrate. Neurite lengths were compared in the presence or absence of monovalent antibodies against specific neural cell surface glycoproteins. Fab fragments of antibodies against the neural cell adhesion molecule, NCAM, have an insignificant effect on the lengths of neurites elongating on either an axonal substrate or a laminin substrate. Fab fragments of polyclonal antibodies against two new neural cell surface antigens, defined by mAb G4 and mAb F11, decrease the lengths of neurites elongating on an axonal substrate, but have no effect on the lengths of neurites elongating on a laminin substrate. G4 antigen is related to mouse L1, while F11 antigen appears to be distinct from all known neural cell surface glycoproteins. Our results suggest that the G4 and F11 antigens help to promote the extension of growth cones on axons. The Rockefeller University Press 1987-02-01 /pmc/articles/PMC2114414/ /pubmed/3543026 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins
title Extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins
title_full Extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins
title_fullStr Extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins
title_full_unstemmed Extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins
title_short Extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins
title_sort extension of neurites on axons is impaired by antibodies against specific neural cell surface glycoproteins
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114414/
https://www.ncbi.nlm.nih.gov/pubmed/3543026