Sphingosine Toxicity in EAE and MS: Evidence for Ceramide Generation via Serine-Palmitoyltransferase Activation

Lawrence G. Miller, Jennifer A. Young, Swapan K. Ray, Guanghu Wang, Sharad B Purohit, Naren L. Banik, Somsankar Dasgupta

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Multiple sclerosis (MS) is a demyelinating disorder characterized by massive neurodegeneration and profound axonal loss. Since myelin is enriched with sphingolipids and some of them display toxicity, biological function of sphingolipids in demyelination has been investigated in MS brain tissues. An elevation of sphingosine with a decrease in monoglycosylceramide and psychosine (myelin markers) was observed in MS white matter and plaque compared to normal brain tissue. This indicated that sphingosine toxicity might mediate oligodendrocyte degeneration. To explain the source of sphingosine accumulation, total sphingolipid profile was investigated in Lewis rats after inducing experimental autoimmune encephalomyelitis (EAE) and also in human oligodendrocytes in culture. An intermittent increase in ceramide followed by sphingosine accumulation in EAE spinal cord along with a stimulation of serine-palmitoyltransferase (SPT) activity was observed. Apoptosis was identified in the lumbar spinal cord, the most prominent demyelinating area, in the EAE rats. TNFα and IFNγ stimulation of oligodendrocytes in culture also led to an accumulation of ceramide with an elevation of sphingosine. Ceramide elevation was drastically blocked by myriocin, an inhibitor of SPT, and also by FTY720. Myriocin treatment also protected oligodendrocytes from cytokine mediated apoptosis or programmed cell death. Hence, we propose that sphingosine toxicity may contribute to demyelination in both EAE and MS, and the intermittent ceramide accumulation in EAE may, at least partly, be mediated via SPT activation, which is a novel observation that has not been previously reported.

Original languageEnglish (US)
Pages (from-to)2755-2768
Number of pages14
JournalNeurochemical Research
Volume42
Issue number10
DOIs
StatePublished - Oct 1 2017

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Serine C-Palmitoyltransferase
Sphingosine
Autoimmune Experimental Encephalomyelitis
Ceramides
Multiple Sclerosis
Toxicity
Chemical activation
Oligodendroglia
Sphingolipids
Demyelinating Diseases
Spinal Cord
Myelin Sheath
Rats
Brain
Psychosine
Tissue
Apoptosis
Cell death
Cell Death
Observation

Keywords

  • Ceramide
  • Demyelination
  • EAE
  • Multiple sclerosis
  • Normal appearing white matter
  • Serine-palmitoyltransferase

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

Cite this

Sphingosine Toxicity in EAE and MS : Evidence for Ceramide Generation via Serine-Palmitoyltransferase Activation. / Miller, Lawrence G.; Young, Jennifer A.; Ray, Swapan K.; Wang, Guanghu; Purohit, Sharad B; Banik, Naren L.; Dasgupta, Somsankar.

In: Neurochemical Research, Vol. 42, No. 10, 01.10.2017, p. 2755-2768.

Research output: Contribution to journalArticle

Miller, Lawrence G. ; Young, Jennifer A. ; Ray, Swapan K. ; Wang, Guanghu ; Purohit, Sharad B ; Banik, Naren L. ; Dasgupta, Somsankar. / Sphingosine Toxicity in EAE and MS : Evidence for Ceramide Generation via Serine-Palmitoyltransferase Activation. In: Neurochemical Research. 2017 ; Vol. 42, No. 10. pp. 2755-2768.
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