Cargando…
Behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating Schwann cells
In inflammatory peripheral demyelinating disorders, demyelination represents segmental demyelination in which the myelin sheath of a myelinating Schwann cell (SC) is completely removed by macrophages or a partial myelin degeneration in the paranode occurring due to autoantibodies attacking the node/...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320037/ https://www.ncbi.nlm.nih.gov/pubmed/31884566 http://dx.doi.org/10.1007/s00018-019-03431-8 |
_version_ | 1783551166438703104 |
---|---|
author | Park, Hwan Tae Kim, Young Hee Lee, Kyung Eun Kim, Jong Kuk |
author_facet | Park, Hwan Tae Kim, Young Hee Lee, Kyung Eun Kim, Jong Kuk |
author_sort | Park, Hwan Tae |
collection | PubMed |
description | In inflammatory peripheral demyelinating disorders, demyelination represents segmental demyelination in which the myelin sheath of a myelinating Schwann cell (SC) is completely removed by macrophages or a partial myelin degeneration in the paranode occurring due to autoantibodies attacking the node/paranode. For the segmental demyelination from living myelin-forming SCs, macrophages infiltrate within the endoneurium and insinuate between myelin lamellae and the cytoplasm of SCs, and the myelin is then removed via phagocytosis. During the macrophage invasion into the SC cytoplasm from the node of Ranvier and internodal areas, the attacked SCs do not remain quiescent but transdifferentiate into inflammatory demyelinating SCs (iDSCs), which exhibit unique demyelination pathologies, such as myelin uncompaction from Schmidt-Lanterman incisures with myelin lamellae degeneration. The longitudinal extension of this self-myelin clearance process of iDSCs into the nodal region is associated with the degeneration of nodal microvilli and paranodal loops, which provides a potential locus for macrophage infiltration. In addition to the nodal intrusion, macrophages appear to be able to invade fenestrated internodal plasma membrane or the degenerated outer mesaxon of iDSC. These SC demyelination morphologies indicate that the SC reprogramming to iDSCs may be a prerequisite for macrophage-mediated inflammatory demyelination. In contrast, paranodal demyelination caused by autoantibodies to nodal/paranodal antigens does not result in iDSC-dependent macrophage infiltration and subsequent segmental demyelination. In the context of inflammatory demyelination, the novel perspective of iDSCs provides an important viewpoint to understand the pathophysiology of demyelinating peripheral neuropathies and establish diagnostic and therapeutic strategies. |
format | Online Article Text |
id | pubmed-7320037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-73200372020-07-01 Behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating Schwann cells Park, Hwan Tae Kim, Young Hee Lee, Kyung Eun Kim, Jong Kuk Cell Mol Life Sci Review In inflammatory peripheral demyelinating disorders, demyelination represents segmental demyelination in which the myelin sheath of a myelinating Schwann cell (SC) is completely removed by macrophages or a partial myelin degeneration in the paranode occurring due to autoantibodies attacking the node/paranode. For the segmental demyelination from living myelin-forming SCs, macrophages infiltrate within the endoneurium and insinuate between myelin lamellae and the cytoplasm of SCs, and the myelin is then removed via phagocytosis. During the macrophage invasion into the SC cytoplasm from the node of Ranvier and internodal areas, the attacked SCs do not remain quiescent but transdifferentiate into inflammatory demyelinating SCs (iDSCs), which exhibit unique demyelination pathologies, such as myelin uncompaction from Schmidt-Lanterman incisures with myelin lamellae degeneration. The longitudinal extension of this self-myelin clearance process of iDSCs into the nodal region is associated with the degeneration of nodal microvilli and paranodal loops, which provides a potential locus for macrophage infiltration. In addition to the nodal intrusion, macrophages appear to be able to invade fenestrated internodal plasma membrane or the degenerated outer mesaxon of iDSC. These SC demyelination morphologies indicate that the SC reprogramming to iDSCs may be a prerequisite for macrophage-mediated inflammatory demyelination. In contrast, paranodal demyelination caused by autoantibodies to nodal/paranodal antigens does not result in iDSC-dependent macrophage infiltration and subsequent segmental demyelination. In the context of inflammatory demyelination, the novel perspective of iDSCs provides an important viewpoint to understand the pathophysiology of demyelinating peripheral neuropathies and establish diagnostic and therapeutic strategies. Springer International Publishing 2019-12-28 2020 /pmc/articles/PMC7320037/ /pubmed/31884566 http://dx.doi.org/10.1007/s00018-019-03431-8 Text en © The Author(s) 2019 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Park, Hwan Tae Kim, Young Hee Lee, Kyung Eun Kim, Jong Kuk Behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating Schwann cells |
title | Behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating Schwann cells |
title_full | Behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating Schwann cells |
title_fullStr | Behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating Schwann cells |
title_full_unstemmed | Behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating Schwann cells |
title_short | Behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating Schwann cells |
title_sort | behind the pathology of macrophage-associated demyelination in inflammatory neuropathies: demyelinating schwann cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320037/ https://www.ncbi.nlm.nih.gov/pubmed/31884566 http://dx.doi.org/10.1007/s00018-019-03431-8 |
work_keys_str_mv | AT parkhwantae behindthepathologyofmacrophageassociateddemyelinationininflammatoryneuropathiesdemyelinatingschwanncells AT kimyounghee behindthepathologyofmacrophageassociateddemyelinationininflammatoryneuropathiesdemyelinatingschwanncells AT leekyungeun behindthepathologyofmacrophageassociateddemyelinationininflammatoryneuropathiesdemyelinatingschwanncells AT kimjongkuk behindthepathologyofmacrophageassociateddemyelinationininflammatoryneuropathiesdemyelinatingschwanncells |