Neutralization of LINGO-1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons.

Identifying external factors that can be used to control neural stem cells division and their differentiation to neurons, astrocytes and oligodendrocytes is of high scientific and clinical interest. Here we show that the Nogo-66 receptor interacting protein LINGO-1 is a potent regulator of neural st...

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Main Authors: Camilla Lööv, Maria Fernqvist, Adrian Walmsley, Niklas Marklund, Anna Erlandsson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3250485?pdf=render
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author Camilla Lööv
Maria Fernqvist
Adrian Walmsley
Niklas Marklund
Anna Erlandsson
author_facet Camilla Lööv
Maria Fernqvist
Adrian Walmsley
Niklas Marklund
Anna Erlandsson
author_sort Camilla Lööv
collection DOAJ
description Identifying external factors that can be used to control neural stem cells division and their differentiation to neurons, astrocytes and oligodendrocytes is of high scientific and clinical interest. Here we show that the Nogo-66 receptor interacting protein LINGO-1 is a potent regulator of neural stem cell maturation to neurons. LINGO-1 is expressed by cortical neural stem cells from E14 mouse embryos and inhibition of LINGO-1 during the first days of neural stem cell differentiation results in decreased neuronal maturation. Compared to neurons in control cultures, which after 6 days of differentiation have long extending neurites, neurons in cultures treated with anti-LINGO-1 antibodies retain an immature, round phenotype with only very short processes. Furthermore, neutralization of LINGO-1 results in a threefold increase in βIII tubulin-positive cells compared to untreated control cultures. By using BrdU incorporation assays we show that the immature neurons in LINGO-1 neutralized cultures are dividing neuroblasts. In contrast to control cultures, in which no cells were double positive for βIII tubulin and BrdU, 36% of the neurons in cultures treated with anti-LINGO-1 antibodies were proliferating after three days of differentiation. TUNEL assays revealed that the amount of cells going through apoptosis during the early phase of differentiation was significantly decreased in cultures treated with anti-LINGO-1 antibodies compared to untreated control cultures. Taken together, our results demonstrate a novel role for LINGO-1 in neural stem cell differentiation to neurons and suggest a possibility to use LINGO-1 inhibitors to compensate for neuronal cell loss in the injured brain.
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spelling doaj.art-0b16731f7040499dae9d0acf9489a4842022-12-21T23:01:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0171e2977110.1371/journal.pone.0029771Neutralization of LINGO-1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons.Camilla LöövMaria FernqvistAdrian WalmsleyNiklas MarklundAnna ErlandssonIdentifying external factors that can be used to control neural stem cells division and their differentiation to neurons, astrocytes and oligodendrocytes is of high scientific and clinical interest. Here we show that the Nogo-66 receptor interacting protein LINGO-1 is a potent regulator of neural stem cell maturation to neurons. LINGO-1 is expressed by cortical neural stem cells from E14 mouse embryos and inhibition of LINGO-1 during the first days of neural stem cell differentiation results in decreased neuronal maturation. Compared to neurons in control cultures, which after 6 days of differentiation have long extending neurites, neurons in cultures treated with anti-LINGO-1 antibodies retain an immature, round phenotype with only very short processes. Furthermore, neutralization of LINGO-1 results in a threefold increase in βIII tubulin-positive cells compared to untreated control cultures. By using BrdU incorporation assays we show that the immature neurons in LINGO-1 neutralized cultures are dividing neuroblasts. In contrast to control cultures, in which no cells were double positive for βIII tubulin and BrdU, 36% of the neurons in cultures treated with anti-LINGO-1 antibodies were proliferating after three days of differentiation. TUNEL assays revealed that the amount of cells going through apoptosis during the early phase of differentiation was significantly decreased in cultures treated with anti-LINGO-1 antibodies compared to untreated control cultures. Taken together, our results demonstrate a novel role for LINGO-1 in neural stem cell differentiation to neurons and suggest a possibility to use LINGO-1 inhibitors to compensate for neuronal cell loss in the injured brain.http://europepmc.org/articles/PMC3250485?pdf=render
spellingShingle Camilla Lööv
Maria Fernqvist
Adrian Walmsley
Niklas Marklund
Anna Erlandsson
Neutralization of LINGO-1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons.
PLoS ONE
title Neutralization of LINGO-1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons.
title_full Neutralization of LINGO-1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons.
title_fullStr Neutralization of LINGO-1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons.
title_full_unstemmed Neutralization of LINGO-1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons.
title_short Neutralization of LINGO-1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons.
title_sort neutralization of lingo 1 during in vitro differentiation of neural stem cells results in proliferation of immature neurons
url http://europepmc.org/articles/PMC3250485?pdf=render
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