Sphingolipids: Important Players in Multiple Sclerosis

Multiple Sclerosis (MS) is the most common cause for permanent disability in young adults. Current pathophysiological understanding has identified an autoaggressive immune reaction with infiltration of immune cells into the central nervous system and local inflammatory and demyelinating reactions. T...

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Main Authors: Ramona Halmer, Silke Walter, Klaus Faßbender
Format: Article
Language:English
Published: Cell Physiol Biochem Press GmbH & Co KG 2014-06-01
Series:Cellular Physiology and Biochemistry
Subjects:
Online Access:http://www.karger.com/Article/FullText/362988
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spelling doaj-9515139717e4495fb41fcb6e9c6c17fb2020-11-25T01:00:16ZengCell Physiol Biochem Press GmbH & Co KGCellular Physiology and Biochemistry1015-89871421-97782014-06-0134111111810.1159/000362988362988Sphingolipids: Important Players in Multiple SclerosisRamona HalmerSilke WalterKlaus FaßbenderMultiple Sclerosis (MS) is the most common cause for permanent disability in young adults. Current pathophysiological understanding has identified an autoaggressive immune reaction with infiltration of immune cells into the central nervous system and local inflammatory and demyelinating reactions. The current therapy focuses on a modulation or suppression of immune functions. Sphingolipids, main components of nervous tissue, have been linked to MS already 60 years ago with the description of an unusual myelin lipid distribution in diseased patients. There is tremendous information developing on the role of different sphingolipids in MS. Antibodies against sphingomyelin, sulfatide or galacosylceramide have been detected in serum or CSF of MS patients, although up to now, this knowledge did not find its way into clinical use. Ceramide and the enzymes linked to its production have been described to play a pivotal role in oligendrocyte damage and demyelination. Nowadays, especially sphingosine-1-phosphate (S1P) is in the focus of pathophysiological research and therapy development. A S1P analogue, FTY720, is a widely distributed therapy against relapsing-remitting MS, attenuating the emigration of activated, autoreactive lymphocytes from lymph nodes, thereby preventing new inflammatory infiltration into the central nervous system. Beside, there is more and more evidence, that especially S1P receptors on oligodendrocytes and astrocytes are involved in demyelination processes and subsequent axonal degeneration, important features of chonic progressive MS disease course. Further information and research on the manifold role of sphingolipids are needed to prepare the ground for further clinical trials. This review focuses on the current knowledge of the role of sphingolipids in MS and describes the current therapeutical implications.http://www.karger.com/Article/FullText/362988Multiple SclerosisSphingomyelinaseSphingolipidsCeramideSphingomyelinSphingosine-1-phosphate
collection DOAJ
language English
format Article
sources DOAJ
author Ramona Halmer
Silke Walter
Klaus Faßbender
spellingShingle Ramona Halmer
Silke Walter
Klaus Faßbender
Sphingolipids: Important Players in Multiple Sclerosis
Cellular Physiology and Biochemistry
Multiple Sclerosis
Sphingomyelinase
Sphingolipids
Ceramide
Sphingomyelin
Sphingosine-1-phosphate
author_facet Ramona Halmer
Silke Walter
Klaus Faßbender
author_sort Ramona Halmer
title Sphingolipids: Important Players in Multiple Sclerosis
title_short Sphingolipids: Important Players in Multiple Sclerosis
title_full Sphingolipids: Important Players in Multiple Sclerosis
title_fullStr Sphingolipids: Important Players in Multiple Sclerosis
title_full_unstemmed Sphingolipids: Important Players in Multiple Sclerosis
title_sort sphingolipids: important players in multiple sclerosis
publisher Cell Physiol Biochem Press GmbH & Co KG
series Cellular Physiology and Biochemistry
issn 1015-8987
1421-9778
publishDate 2014-06-01
description Multiple Sclerosis (MS) is the most common cause for permanent disability in young adults. Current pathophysiological understanding has identified an autoaggressive immune reaction with infiltration of immune cells into the central nervous system and local inflammatory and demyelinating reactions. The current therapy focuses on a modulation or suppression of immune functions. Sphingolipids, main components of nervous tissue, have been linked to MS already 60 years ago with the description of an unusual myelin lipid distribution in diseased patients. There is tremendous information developing on the role of different sphingolipids in MS. Antibodies against sphingomyelin, sulfatide or galacosylceramide have been detected in serum or CSF of MS patients, although up to now, this knowledge did not find its way into clinical use. Ceramide and the enzymes linked to its production have been described to play a pivotal role in oligendrocyte damage and demyelination. Nowadays, especially sphingosine-1-phosphate (S1P) is in the focus of pathophysiological research and therapy development. A S1P analogue, FTY720, is a widely distributed therapy against relapsing-remitting MS, attenuating the emigration of activated, autoreactive lymphocytes from lymph nodes, thereby preventing new inflammatory infiltration into the central nervous system. Beside, there is more and more evidence, that especially S1P receptors on oligodendrocytes and astrocytes are involved in demyelination processes and subsequent axonal degeneration, important features of chonic progressive MS disease course. Further information and research on the manifold role of sphingolipids are needed to prepare the ground for further clinical trials. This review focuses on the current knowledge of the role of sphingolipids in MS and describes the current therapeutical implications.
topic Multiple Sclerosis
Sphingomyelinase
Sphingolipids
Ceramide
Sphingomyelin
Sphingosine-1-phosphate
url http://www.karger.com/Article/FullText/362988
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