HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Candida albicans phospholipomannan: a sweet spot for controlling host response/inflammation.

Abstract
Fungal cell walls contain several types of glycans, which play important roles in the pathogenesis of fungal infection and host immune response. Among them, glycosphingolipids have attracted much attention lately since they contribute actively to the fungi development and fungal-induced pathogenesis. Although glycosphingolipids are present in pathogenic and non-pathogenic fungi, pathogenic strains exhibit distinct glycan structures on their sphingolipids, which contribute to the regulatory processes engaged in inflammatory response. In Candida albicans, phospholipomannan (PLM) represents a prototype of these sphingolipids. Through its glycan and lipid moieties, PLM induces activation of host signaling pathways involved in the initial recognition of fungi, causing immune system disorder and persistent fungal disease. In this review, first we describe the general aspects of C. albicans sphingolipids synthesis with a special emphasize on PLM synthesis and its insertion into the cell wall. Then, we discuss the role of PLM glycosylation in regulating immune system activation and its contribution to the chronic persistent inflammation found in Candida infections and chronic inflammatory diseases.
AuthorsChantal Fradin, Emerson Soares Bernardes, Thierry Jouault
JournalSeminars in immunopathology (Semin Immunopathol) Vol. 37 Issue 2 Pg. 123-30 (Mar 2015) ISSN: 1863-2300 [Electronic] Germany
PMID25394861 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Glycolipids
  • Glycosphingolipids
  • Polysaccharides
  • Receptors, Pattern Recognition
  • Sphingolipids
  • phospholipomannan
Topics
  • Candida albicans (immunology, metabolism, pathogenicity)
  • Candidiasis (immunology, metabolism)
  • Glycolipids (metabolism)
  • Glycosphingolipids (biosynthesis)
  • Host-Pathogen Interactions (immunology)
  • Humans
  • Immunomodulation
  • Macrophage Activation (immunology)
  • Macrophages (immunology, metabolism)
  • Polysaccharides (immunology, metabolism)
  • Receptors, Pattern Recognition (metabolism)
  • Signal Transduction
  • Sphingolipids (biosynthesis)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: