Polysialic acid modification of the synaptic cell adhesion molecule SynCAM 1 in human embryonic stem cell-derived oligodendrocyte precursor cells

Oligodendrocyte precursor cells (OPCs) are the progenitors of myelinating oligodendrocytes in brain development and repair. Successful myelination depends on the control of adhesiveness during OPC migration and axon contact formation. The decoration of cell surface proteins with the glycan polysiali...

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Main Authors: Sebastian Werneburg, Falk F.R. Buettner, Martina Mühlenhoff, Herbert Hildebrandt
Format: Article
Language:English
Published: Elsevier 2015-05-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506115000410
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author Sebastian Werneburg
Falk F.R. Buettner
Martina Mühlenhoff
Herbert Hildebrandt
author_facet Sebastian Werneburg
Falk F.R. Buettner
Martina Mühlenhoff
Herbert Hildebrandt
author_sort Sebastian Werneburg
collection DOAJ
description Oligodendrocyte precursor cells (OPCs) are the progenitors of myelinating oligodendrocytes in brain development and repair. Successful myelination depends on the control of adhesiveness during OPC migration and axon contact formation. The decoration of cell surface proteins with the glycan polysialic acid (polySia) is a key regulatory element of OPC interactions during development and under pathological conditions. By far the major protein carrier of polySia is the neural cell adhesion molecule NCAM, but recently, polysialylation of the synaptic cell adhesion molecule SynCAM 1 has been detected in the developing mouse brain. In mice, polySia-SynCAM 1 is associated with cells expressing NG2, a marker of a heterogeneous precursor cell population, which is the primary source for oligodendrocytes in development and myelin repair but can also give rise to astrocytes and possibly neurons. It is not yet clear if polySia-SynCAM 1 is expressed by OPCs and its occurrence in humans is elusive. By generating uniform human embryonic stem cell-derived OPC cultures, we demonstrate that polySia is present on human OPCs but down-regulated during differentiation into myelin basic protein-positive oligodendrocytes. PolySia on NCAM resides on the isoforms NCAM-180 and NCAM-140, and SynCAM 1 is identified as a novel polySia acceptor in human OPCs.
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spelling doaj.art-3382f1f3cac64472987a855d5ea7b7b92022-12-22T03:56:35ZengElsevierStem Cell Research1873-50611876-77532015-05-0114333934610.1016/j.scr.2015.03.001Polysialic acid modification of the synaptic cell adhesion molecule SynCAM 1 in human embryonic stem cell-derived oligodendrocyte precursor cellsSebastian Werneburg0Falk F.R. Buettner1Martina Mühlenhoff2Herbert Hildebrandt3Institute for Cellular Chemistry, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, GermanyInstitute for Cellular Chemistry, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, GermanyInstitute for Cellular Chemistry, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, GermanyInstitute for Cellular Chemistry, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, GermanyOligodendrocyte precursor cells (OPCs) are the progenitors of myelinating oligodendrocytes in brain development and repair. Successful myelination depends on the control of adhesiveness during OPC migration and axon contact formation. The decoration of cell surface proteins with the glycan polysialic acid (polySia) is a key regulatory element of OPC interactions during development and under pathological conditions. By far the major protein carrier of polySia is the neural cell adhesion molecule NCAM, but recently, polysialylation of the synaptic cell adhesion molecule SynCAM 1 has been detected in the developing mouse brain. In mice, polySia-SynCAM 1 is associated with cells expressing NG2, a marker of a heterogeneous precursor cell population, which is the primary source for oligodendrocytes in development and myelin repair but can also give rise to astrocytes and possibly neurons. It is not yet clear if polySia-SynCAM 1 is expressed by OPCs and its occurrence in humans is elusive. By generating uniform human embryonic stem cell-derived OPC cultures, we demonstrate that polySia is present on human OPCs but down-regulated during differentiation into myelin basic protein-positive oligodendrocytes. PolySia on NCAM resides on the isoforms NCAM-180 and NCAM-140, and SynCAM 1 is identified as a novel polySia acceptor in human OPCs.http://www.sciencedirect.com/science/article/pii/S1873506115000410
spellingShingle Sebastian Werneburg
Falk F.R. Buettner
Martina Mühlenhoff
Herbert Hildebrandt
Polysialic acid modification of the synaptic cell adhesion molecule SynCAM 1 in human embryonic stem cell-derived oligodendrocyte precursor cells
Stem Cell Research
title Polysialic acid modification of the synaptic cell adhesion molecule SynCAM 1 in human embryonic stem cell-derived oligodendrocyte precursor cells
title_full Polysialic acid modification of the synaptic cell adhesion molecule SynCAM 1 in human embryonic stem cell-derived oligodendrocyte precursor cells
title_fullStr Polysialic acid modification of the synaptic cell adhesion molecule SynCAM 1 in human embryonic stem cell-derived oligodendrocyte precursor cells
title_full_unstemmed Polysialic acid modification of the synaptic cell adhesion molecule SynCAM 1 in human embryonic stem cell-derived oligodendrocyte precursor cells
title_short Polysialic acid modification of the synaptic cell adhesion molecule SynCAM 1 in human embryonic stem cell-derived oligodendrocyte precursor cells
title_sort polysialic acid modification of the synaptic cell adhesion molecule syncam 1 in human embryonic stem cell derived oligodendrocyte precursor cells
url http://www.sciencedirect.com/science/article/pii/S1873506115000410
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