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In vitro modulation of Schwann cell behavior by VEGF and PDGF in an inflammatory environment

Peripheral glial cell transplantation with Schwann cells (SCs) is a promising approach for treating spinal cord injury (SCI). However, improvements are needed and one avenue to enhance regenerative functional outcomes is to combine growth factors with cell transplantation. Vascular endothelial growt...

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Autores principales: Basu, Souptik, Choudhury, Indra N., Nazareth, Lynn, Chacko, Anu, Shelper, Todd, Vial, Marie-Laure, Ekberg, Jenny A. K., St John, James A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8758747/
https://www.ncbi.nlm.nih.gov/pubmed/35027585
http://dx.doi.org/10.1038/s41598-021-04222-7
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author Basu, Souptik
Choudhury, Indra N.
Nazareth, Lynn
Chacko, Anu
Shelper, Todd
Vial, Marie-Laure
Ekberg, Jenny A. K.
St John, James A.
author_facet Basu, Souptik
Choudhury, Indra N.
Nazareth, Lynn
Chacko, Anu
Shelper, Todd
Vial, Marie-Laure
Ekberg, Jenny A. K.
St John, James A.
author_sort Basu, Souptik
collection PubMed
description Peripheral glial cell transplantation with Schwann cells (SCs) is a promising approach for treating spinal cord injury (SCI). However, improvements are needed and one avenue to enhance regenerative functional outcomes is to combine growth factors with cell transplantation. Vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) are neuroprotective, and a combination of these factors has improved outcomes in rat SCI models. Thus, transplantation of SCs combined with VEGF and PDGF may further improve regenerative outcomes. First, however, we must understand how the two factors modulate SCs. In this in vitro study, we show that an inflammatory environment decreased the rate of SC-mediated phagocytosis of myelin debris but the addition of VEGF and PDGF (alone and combined) improved phagocytosis. Cytokine expression by SCs in the inflammatory environment revealed that addition of PDGF led to significantly lower level of pro-inflammatory cytokine, TNF-α, but IL-6 and anti-inflammatory cytokines (TGF-β and IL-10), remained unaltered. Further, PDGF was able to decrease the expression of myelination associated gene Oct6 in the presence of inflammatory environment. Overall, these results suggest that the use of VEGF and/or PDGF combined with SC transplantation may be beneficial in SCI therapy.
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spelling pubmed-87587472022-01-14 In vitro modulation of Schwann cell behavior by VEGF and PDGF in an inflammatory environment Basu, Souptik Choudhury, Indra N. Nazareth, Lynn Chacko, Anu Shelper, Todd Vial, Marie-Laure Ekberg, Jenny A. K. St John, James A. Sci Rep Article Peripheral glial cell transplantation with Schwann cells (SCs) is a promising approach for treating spinal cord injury (SCI). However, improvements are needed and one avenue to enhance regenerative functional outcomes is to combine growth factors with cell transplantation. Vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) are neuroprotective, and a combination of these factors has improved outcomes in rat SCI models. Thus, transplantation of SCs combined with VEGF and PDGF may further improve regenerative outcomes. First, however, we must understand how the two factors modulate SCs. In this in vitro study, we show that an inflammatory environment decreased the rate of SC-mediated phagocytosis of myelin debris but the addition of VEGF and PDGF (alone and combined) improved phagocytosis. Cytokine expression by SCs in the inflammatory environment revealed that addition of PDGF led to significantly lower level of pro-inflammatory cytokine, TNF-α, but IL-6 and anti-inflammatory cytokines (TGF-β and IL-10), remained unaltered. Further, PDGF was able to decrease the expression of myelination associated gene Oct6 in the presence of inflammatory environment. Overall, these results suggest that the use of VEGF and/or PDGF combined with SC transplantation may be beneficial in SCI therapy. Nature Publishing Group UK 2022-01-13 /pmc/articles/PMC8758747/ /pubmed/35027585 http://dx.doi.org/10.1038/s41598-021-04222-7 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Basu, Souptik
Choudhury, Indra N.
Nazareth, Lynn
Chacko, Anu
Shelper, Todd
Vial, Marie-Laure
Ekberg, Jenny A. K.
St John, James A.
In vitro modulation of Schwann cell behavior by VEGF and PDGF in an inflammatory environment
title In vitro modulation of Schwann cell behavior by VEGF and PDGF in an inflammatory environment
title_full In vitro modulation of Schwann cell behavior by VEGF and PDGF in an inflammatory environment
title_fullStr In vitro modulation of Schwann cell behavior by VEGF and PDGF in an inflammatory environment
title_full_unstemmed In vitro modulation of Schwann cell behavior by VEGF and PDGF in an inflammatory environment
title_short In vitro modulation of Schwann cell behavior by VEGF and PDGF in an inflammatory environment
title_sort in vitro modulation of schwann cell behavior by vegf and pdgf in an inflammatory environment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8758747/
https://www.ncbi.nlm.nih.gov/pubmed/35027585
http://dx.doi.org/10.1038/s41598-021-04222-7
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