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The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis

Autoimmune diseases of the central nervous system (CNS) like multiple sclerosis (MS) are characterized by inflammation and demyelinated lesions in white and grey matter regions. While inflammation is present at all stages of MS, it is more pronounced in the relapsing forms of the disease, whereas pr...

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Autores principales: Hundehege, Petra, Cerina, Manuela, Eichler, Susann, Thomas, Christian, Herrmann, Alexander M., Göbel, Kerstin, Müntefering, Thomas, Fernandez-Orth, Juncal, Bock, Stefanie, Narayanan, Venu, Budde, Thomas, Speckmann, Erwin-Josef, Wiendl, Heinz, Schubart, Anna, Ruck, Tobias, Meuth, Sven G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676873/
https://www.ncbi.nlm.nih.gov/pubmed/31290453
http://dx.doi.org/10.4103/1673-5374.259622
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author Hundehege, Petra
Cerina, Manuela
Eichler, Susann
Thomas, Christian
Herrmann, Alexander M.
Göbel, Kerstin
Müntefering, Thomas
Fernandez-Orth, Juncal
Bock, Stefanie
Narayanan, Venu
Budde, Thomas
Speckmann, Erwin-Josef
Wiendl, Heinz
Schubart, Anna
Ruck, Tobias
Meuth, Sven G.
author_facet Hundehege, Petra
Cerina, Manuela
Eichler, Susann
Thomas, Christian
Herrmann, Alexander M.
Göbel, Kerstin
Müntefering, Thomas
Fernandez-Orth, Juncal
Bock, Stefanie
Narayanan, Venu
Budde, Thomas
Speckmann, Erwin-Josef
Wiendl, Heinz
Schubart, Anna
Ruck, Tobias
Meuth, Sven G.
author_sort Hundehege, Petra
collection PubMed
description Autoimmune diseases of the central nervous system (CNS) like multiple sclerosis (MS) are characterized by inflammation and demyelinated lesions in white and grey matter regions. While inflammation is present at all stages of MS, it is more pronounced in the relapsing forms of the disease, whereas progressive MS (PMS) shows significant neuroaxonal damage and grey and white matter atrophy. Hence, disease-modifying treatments beneficial in patients with relapsing MS have limited success in PMS. BAF312 (siponimod) is a novel sphingosine-1-phosphate receptor modulator shown to delay progression in PMS. Besides reducing inflammation by sequestering lymphocytes in lymphoid tissues, BAF312 crosses the blood-brain barrier and binds its receptors on neurons, astrocytes and oligodendrocytes. To evaluate potential direct neuroprotective effects, BAF312 was systemically or locally administered in the CNS of experimental autoimmune encephalomyelitis mice with distinct grey- and white-matter lesions (focal experimental autoimmune encephalomyelitis using an osmotic mini-pump). Ex-vivo flow cytometry revealed that systemic but not local BAF312 administration lowered immune cell infiltration in animals with both grey and white matter lesions. Ex-vivo voltage-sensitive dye imaging of acute brain slices revealed an altered spatio-temporal pattern of activation in the lesioned cortex compared to controls in response to electrical stimulation of incoming white-matter fiber tracts. Here, BAF312 administration showed partial restore of cortical neuronal circuit function. The data suggest that BAF312 exerts a neuroprotective effect after crossing the blood-brain barrier independently of peripheral effects on immune cells. Experiments were carried out in accordance with German and EU animal protection law and approved by local authorities (Landesamt für Natur, Umwelt und Verbraucherschutz Nordrhein-Westfalen; 87-51.04.2010.A331) on December 28, 2010.
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spelling pubmed-66768732019-11-01 The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis Hundehege, Petra Cerina, Manuela Eichler, Susann Thomas, Christian Herrmann, Alexander M. Göbel, Kerstin Müntefering, Thomas Fernandez-Orth, Juncal Bock, Stefanie Narayanan, Venu Budde, Thomas Speckmann, Erwin-Josef Wiendl, Heinz Schubart, Anna Ruck, Tobias Meuth, Sven G. Neural Regen Res Research Article Autoimmune diseases of the central nervous system (CNS) like multiple sclerosis (MS) are characterized by inflammation and demyelinated lesions in white and grey matter regions. While inflammation is present at all stages of MS, it is more pronounced in the relapsing forms of the disease, whereas progressive MS (PMS) shows significant neuroaxonal damage and grey and white matter atrophy. Hence, disease-modifying treatments beneficial in patients with relapsing MS have limited success in PMS. BAF312 (siponimod) is a novel sphingosine-1-phosphate receptor modulator shown to delay progression in PMS. Besides reducing inflammation by sequestering lymphocytes in lymphoid tissues, BAF312 crosses the blood-brain barrier and binds its receptors on neurons, astrocytes and oligodendrocytes. To evaluate potential direct neuroprotective effects, BAF312 was systemically or locally administered in the CNS of experimental autoimmune encephalomyelitis mice with distinct grey- and white-matter lesions (focal experimental autoimmune encephalomyelitis using an osmotic mini-pump). Ex-vivo flow cytometry revealed that systemic but not local BAF312 administration lowered immune cell infiltration in animals with both grey and white matter lesions. Ex-vivo voltage-sensitive dye imaging of acute brain slices revealed an altered spatio-temporal pattern of activation in the lesioned cortex compared to controls in response to electrical stimulation of incoming white-matter fiber tracts. Here, BAF312 administration showed partial restore of cortical neuronal circuit function. The data suggest that BAF312 exerts a neuroprotective effect after crossing the blood-brain barrier independently of peripheral effects on immune cells. Experiments were carried out in accordance with German and EU animal protection law and approved by local authorities (Landesamt für Natur, Umwelt und Verbraucherschutz Nordrhein-Westfalen; 87-51.04.2010.A331) on December 28, 2010. Wolters Kluwer - Medknow 2019-11 /pmc/articles/PMC6676873/ /pubmed/31290453 http://dx.doi.org/10.4103/1673-5374.259622 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Hundehege, Petra
Cerina, Manuela
Eichler, Susann
Thomas, Christian
Herrmann, Alexander M.
Göbel, Kerstin
Müntefering, Thomas
Fernandez-Orth, Juncal
Bock, Stefanie
Narayanan, Venu
Budde, Thomas
Speckmann, Erwin-Josef
Wiendl, Heinz
Schubart, Anna
Ruck, Tobias
Meuth, Sven G.
The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis
title The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis
title_full The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis
title_fullStr The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis
title_full_unstemmed The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis
title_short The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis
title_sort next-generation sphingosine-1 receptor modulator baf312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676873/
https://www.ncbi.nlm.nih.gov/pubmed/31290453
http://dx.doi.org/10.4103/1673-5374.259622
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