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An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction

Two major isoforms of the cell adhesion molecule neurofascin NF186 and NF155 are expressed in the central nervous system (CNS). We have investigated their roles in the assembly of the node of Ranvier and show that they are targeted to distinct domains at the node. At the onset of myelination, NF186...

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Autores principales: Tait, Steven, Gunn-Moore, Frank, Collinson, J. Martin, Huang, Jeffery, Lubetzki, Catherine, Pedraza, Liliana, Sherman, Diane L., Colman, David R., Brophy, Peter J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175192/
https://www.ncbi.nlm.nih.gov/pubmed/10931875
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author Tait, Steven
Gunn-Moore, Frank
Collinson, J. Martin
Huang, Jeffery
Lubetzki, Catherine
Pedraza, Liliana
Sherman, Diane L.
Colman, David R.
Brophy, Peter J.
author_facet Tait, Steven
Gunn-Moore, Frank
Collinson, J. Martin
Huang, Jeffery
Lubetzki, Catherine
Pedraza, Liliana
Sherman, Diane L.
Colman, David R.
Brophy, Peter J.
author_sort Tait, Steven
collection PubMed
description Two major isoforms of the cell adhesion molecule neurofascin NF186 and NF155 are expressed in the central nervous system (CNS). We have investigated their roles in the assembly of the node of Ranvier and show that they are targeted to distinct domains at the node. At the onset of myelination, NF186 is restricted to neurons, whereas NF155 localizes to oligodendrocytes, the myelin-forming glia of the CNS. Coincident with axon ensheathment, NF155 clusters at the paranodal regions of the myelin sheath where it localizes in apposition to the axonal adhesion molecule paranodin/contactin-associated protein (Caspr1), which is a constituent of the septate junction-like axo-glial adhesion zone. Immunoelectron microscopy confirmed that neurofascin is a glial component of the paranodal axo-glial junction. Concentration of NF155 with Caspr1 at the paranodal junctions of peripheral nerves is also a feature of Schwann cells. In Shiverer mutant mice, which assemble neither compact CNS myelin nor normal paranodes, NF155 (though largely retained at the cell body) is also distributed at ectopic sites along axons, where it colocalizes with Caspr1. Hence, NF155 is the first glial cell adhesion molecule to be identified in the paranodal axo-glial junction, where it likely interacts with axonal proteins in close association with Caspr1.
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spelling pubmed-21751922008-05-01 An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction Tait, Steven Gunn-Moore, Frank Collinson, J. Martin Huang, Jeffery Lubetzki, Catherine Pedraza, Liliana Sherman, Diane L. Colman, David R. Brophy, Peter J. J Cell Biol Original Article Two major isoforms of the cell adhesion molecule neurofascin NF186 and NF155 are expressed in the central nervous system (CNS). We have investigated their roles in the assembly of the node of Ranvier and show that they are targeted to distinct domains at the node. At the onset of myelination, NF186 is restricted to neurons, whereas NF155 localizes to oligodendrocytes, the myelin-forming glia of the CNS. Coincident with axon ensheathment, NF155 clusters at the paranodal regions of the myelin sheath where it localizes in apposition to the axonal adhesion molecule paranodin/contactin-associated protein (Caspr1), which is a constituent of the septate junction-like axo-glial adhesion zone. Immunoelectron microscopy confirmed that neurofascin is a glial component of the paranodal axo-glial junction. Concentration of NF155 with Caspr1 at the paranodal junctions of peripheral nerves is also a feature of Schwann cells. In Shiverer mutant mice, which assemble neither compact CNS myelin nor normal paranodes, NF155 (though largely retained at the cell body) is also distributed at ectopic sites along axons, where it colocalizes with Caspr1. Hence, NF155 is the first glial cell adhesion molecule to be identified in the paranodal axo-glial junction, where it likely interacts with axonal proteins in close association with Caspr1. The Rockefeller University Press 2000-08-07 /pmc/articles/PMC2175192/ /pubmed/10931875 Text en © 2000 The Rockefeller University Press 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 Original Article
Tait, Steven
Gunn-Moore, Frank
Collinson, J. Martin
Huang, Jeffery
Lubetzki, Catherine
Pedraza, Liliana
Sherman, Diane L.
Colman, David R.
Brophy, Peter J.
An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction
title An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction
title_full An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction
title_fullStr An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction
title_full_unstemmed An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction
title_short An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction
title_sort oligodendrocyte cell adhesion molecule at the site of assembly of the paranodal axo-glial junction
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175192/
https://www.ncbi.nlm.nih.gov/pubmed/10931875
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