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Bone marrow stromal cells in Modic type 1 changes promote neurite outgrowth
The pain in patients with Modic type 1 changes (MC1) is often due to vertebral body endplate pain, which is linked to abnormal neurite outgrowth in the vertebral body and adjacent endplate. The aim of this study was to understand the role of MC1 bone marrow stromal cells (BMSCs) in neurite outgrowth...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641389/ https://www.ncbi.nlm.nih.gov/pubmed/37965581 http://dx.doi.org/10.3389/fcell.2023.1286280 |
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author | Mengis, Tamara Herger, Nick Heggli, Irina Devan, Jan Spirig, José Miguel Laux, Christoph J. Brunner, Florian Farshad, Mazda Distler, Oliver Dudli, Stefan |
author_facet | Mengis, Tamara Herger, Nick Heggli, Irina Devan, Jan Spirig, José Miguel Laux, Christoph J. Brunner, Florian Farshad, Mazda Distler, Oliver Dudli, Stefan |
author_sort | Mengis, Tamara |
collection | PubMed |
description | The pain in patients with Modic type 1 changes (MC1) is often due to vertebral body endplate pain, which is linked to abnormal neurite outgrowth in the vertebral body and adjacent endplate. The aim of this study was to understand the role of MC1 bone marrow stromal cells (BMSCs) in neurite outgrowth. BMSCs can produce neurotrophic factors, which have been shown to be pro-fibrotic in MC1, and expand in the perivascular space where sensory vertebral nerves are located. The study involved the exploration of the BMSC transcriptome in MC1, co-culture of MC1 BMSCs with the neuroblastoma cell line SH-SY5Y, analysis of supernatant cytokines, and analysis of gene expression changes in co-cultured SH-SY5Y. Transcriptomic analysis revealed upregulated brain-derived neurotrophic factor (BDNF) signaling-related pathways. Co-cultures of MC1 BMSCs with SH-SY5Y cells resulted in increased neurite sprouting compared to co-cultures with control BMSCs. The concentration of BDNF and other cytokines supporting neuron growth was increased in MC1 vs. control BMSC co-culture supernatants. Taken together, these findings show that MC1 BMSCs provide strong pro-neurotrophic cues to nearby neurons and could be a relevant disease-modifying treatment target. |
format | Online Article Text |
id | pubmed-10641389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106413892023-11-14 Bone marrow stromal cells in Modic type 1 changes promote neurite outgrowth Mengis, Tamara Herger, Nick Heggli, Irina Devan, Jan Spirig, José Miguel Laux, Christoph J. Brunner, Florian Farshad, Mazda Distler, Oliver Dudli, Stefan Front Cell Dev Biol Cell and Developmental Biology The pain in patients with Modic type 1 changes (MC1) is often due to vertebral body endplate pain, which is linked to abnormal neurite outgrowth in the vertebral body and adjacent endplate. The aim of this study was to understand the role of MC1 bone marrow stromal cells (BMSCs) in neurite outgrowth. BMSCs can produce neurotrophic factors, which have been shown to be pro-fibrotic in MC1, and expand in the perivascular space where sensory vertebral nerves are located. The study involved the exploration of the BMSC transcriptome in MC1, co-culture of MC1 BMSCs with the neuroblastoma cell line SH-SY5Y, analysis of supernatant cytokines, and analysis of gene expression changes in co-cultured SH-SY5Y. Transcriptomic analysis revealed upregulated brain-derived neurotrophic factor (BDNF) signaling-related pathways. Co-cultures of MC1 BMSCs with SH-SY5Y cells resulted in increased neurite sprouting compared to co-cultures with control BMSCs. The concentration of BDNF and other cytokines supporting neuron growth was increased in MC1 vs. control BMSC co-culture supernatants. Taken together, these findings show that MC1 BMSCs provide strong pro-neurotrophic cues to nearby neurons and could be a relevant disease-modifying treatment target. Frontiers Media S.A. 2023-10-25 /pmc/articles/PMC10641389/ /pubmed/37965581 http://dx.doi.org/10.3389/fcell.2023.1286280 Text en Copyright © 2023 Mengis, Herger, Heggli, Devan, Spirig, Laux, Brunner, Farshad, Distler and Dudli. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Mengis, Tamara Herger, Nick Heggli, Irina Devan, Jan Spirig, José Miguel Laux, Christoph J. Brunner, Florian Farshad, Mazda Distler, Oliver Dudli, Stefan Bone marrow stromal cells in Modic type 1 changes promote neurite outgrowth |
title | Bone marrow stromal cells in Modic type 1 changes promote neurite outgrowth |
title_full | Bone marrow stromal cells in Modic type 1 changes promote neurite outgrowth |
title_fullStr | Bone marrow stromal cells in Modic type 1 changes promote neurite outgrowth |
title_full_unstemmed | Bone marrow stromal cells in Modic type 1 changes promote neurite outgrowth |
title_short | Bone marrow stromal cells in Modic type 1 changes promote neurite outgrowth |
title_sort | bone marrow stromal cells in modic type 1 changes promote neurite outgrowth |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641389/ https://www.ncbi.nlm.nih.gov/pubmed/37965581 http://dx.doi.org/10.3389/fcell.2023.1286280 |
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