Sphingolipids in neuroinflammation: A potential target for diagnosis and therapy

Ju Youn Lee, Hee Kyung Jin, Jae Sung Bae

Research output: Contribution to journalShort surveypeer-review

48 Scopus citations

Abstract

Sphingolipids are ubiquitous building blocks of eukaryotic cell membranes that function as signaling molecules for regulating a diverse range of cellular processes, including cell proliferation, growth, survival, immune-cell trafficking, vascular and epithelial integrity, and inflammation. Recently, several studies have highlighted the pivotal role of sphingolipids in neuroinflammatory regulation. Sphingolipids have multiple functions, including induction of the expression of various inflammatory mediators and regulation of neuroinflammation by directly effecting the cells of the central nervous system. Accumulating evidence points to sphingolipid engagement in neuroinflammatory disorders, including Alzheimer's and Parkinson's diseases. Abnormal sphingolipid alterations, which involves an increase in ceramide and a decrease in sphingosine kinase, are observed during neuroinflammatory disease. These trends are observed early during disease development, and thus highlight the potential of sphingolipids as a new therapeutic and diagnostic target for neuroinflammatory diseases.

Original languageEnglish
Pages (from-to)28-34
Number of pages7
JournalBMB Reports
Volume53
Issue number1
DOIs
StatePublished - 2020
Externally publishedYes

Keywords

  • Alzheimer's disease
  • Ceramide
  • Neuroinflammation
  • Parkinson's disease
  • Sphingosine kinase
  • Sphingosine-1-phosphate

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