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Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration

Myelinated Schwann cells in the peripheral nervous system express the p75 nerve growth factor receptor (p75NGFR) as a consequence of Schwann cell dedifferentiation during Wallerian degeneration. p75NGFR has been implicated in the remyelination of regenerating nerves. Although many studies have shown...

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Autores principales: Jung, Junyang, Cai, Wenting, Jang, So Young, Shin, Yoon Kyoung, Suh, Duk Joon, Kim, Jong Kuk, Park, Hwan Tae
Formato: Texto
Lenguaje:English
Publicado: Korean Association of Anatomists 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080007/
https://www.ncbi.nlm.nih.gov/pubmed/21519548
http://dx.doi.org/10.5115/acb.2011.44.1.41
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author Jung, Junyang
Cai, Wenting
Jang, So Young
Shin, Yoon Kyoung
Suh, Duk Joon
Kim, Jong Kuk
Park, Hwan Tae
author_facet Jung, Junyang
Cai, Wenting
Jang, So Young
Shin, Yoon Kyoung
Suh, Duk Joon
Kim, Jong Kuk
Park, Hwan Tae
author_sort Jung, Junyang
collection PubMed
description Myelinated Schwann cells in the peripheral nervous system express the p75 nerve growth factor receptor (p75NGFR) as a consequence of Schwann cell dedifferentiation during Wallerian degeneration. p75NGFR has been implicated in the remyelination of regenerating nerves. Although many studies have shown various mechanisms underlying Schwann cell dedifferentiation, the molecular mechanism contributing to the re-expression of p75NGFR in differentiated Schwann cells is largely unknown. In the present study, we found that lysosomes were transiently activated in Schwann cells after nerve injury and that the inhibition of lysosomal activation by chloroquine or lysosomal acidification inhibitors prevented p75NGFR expression at the mRNA transcriptional level in an ex vivo Wallerian degeneration model. Lysosomal acidification inhibitors suppressed demyelination, but not axonal degeneration, thereby suggesting that demyelination mediated by lysosomes may be an important signal for inducing p75NGFR expression. Tumor necrosis factor-α (TNF-α) has been suggested to be involved in regulating p75NGFR expression in Schwann cells. In this study, we found that removing TNF-α in vivo did not significantly suppress the induction of both lysosomes and p75NGFR. Thus, these findings suggest that lysosomal activation is tightly correlated with the induction of p75NGFR in demyelinating Schwann cells during Wallerian degeneration.
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spelling pubmed-30800072011-04-25 Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration Jung, Junyang Cai, Wenting Jang, So Young Shin, Yoon Kyoung Suh, Duk Joon Kim, Jong Kuk Park, Hwan Tae Anat Cell Biol Original Article Myelinated Schwann cells in the peripheral nervous system express the p75 nerve growth factor receptor (p75NGFR) as a consequence of Schwann cell dedifferentiation during Wallerian degeneration. p75NGFR has been implicated in the remyelination of regenerating nerves. Although many studies have shown various mechanisms underlying Schwann cell dedifferentiation, the molecular mechanism contributing to the re-expression of p75NGFR in differentiated Schwann cells is largely unknown. In the present study, we found that lysosomes were transiently activated in Schwann cells after nerve injury and that the inhibition of lysosomal activation by chloroquine or lysosomal acidification inhibitors prevented p75NGFR expression at the mRNA transcriptional level in an ex vivo Wallerian degeneration model. Lysosomal acidification inhibitors suppressed demyelination, but not axonal degeneration, thereby suggesting that demyelination mediated by lysosomes may be an important signal for inducing p75NGFR expression. Tumor necrosis factor-α (TNF-α) has been suggested to be involved in regulating p75NGFR expression in Schwann cells. In this study, we found that removing TNF-α in vivo did not significantly suppress the induction of both lysosomes and p75NGFR. Thus, these findings suggest that lysosomal activation is tightly correlated with the induction of p75NGFR in demyelinating Schwann cells during Wallerian degeneration. Korean Association of Anatomists 2011-03 2011-03-31 /pmc/articles/PMC3080007/ /pubmed/21519548 http://dx.doi.org/10.5115/acb.2011.44.1.41 Text en Copyright © 2011. Anatomy & Cell Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jung, Junyang
Cai, Wenting
Jang, So Young
Shin, Yoon Kyoung
Suh, Duk Joon
Kim, Jong Kuk
Park, Hwan Tae
Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration
title Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration
title_full Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration
title_fullStr Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration
title_full_unstemmed Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration
title_short Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration
title_sort transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated schwann cells during wallerian degeneration
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080007/
https://www.ncbi.nlm.nih.gov/pubmed/21519548
http://dx.doi.org/10.5115/acb.2011.44.1.41
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