HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Specific sphingolipid content decrease in Cerkl knockdown mouse retinas.

Abstract
Sphingolipids (SPLs) are finely tuned structural compounds and bioactive molecules involved in membrane fluidity and cellular homeostasis. The core sphingolipid, ceramide (CER), and its derivatives, regulate several crucial processes in neuronal cells, among them cell differentiation, cell-cell interactions, membrane conductance, synaptic transmission, and apoptosis. Mutations in Ceramide Kinase-Like (CERKL) cause autosomal recessive Retinitis Pigmentosa and Cone Rod Dystrophy. The presence of a conserved lipid kinase domain and the overall similarity with CERK suggested that CERKL might play a role in the SPL metabolism as a CER kinase. Unfortunately, CERKL function and substrate(s), as well as its contribution to the retinal etiopathology, remain as yet unknown. In this work we aimed to characterize the mouse retinal sphingolipidome by UPLC-TOF to first, thoroughly investigate the SPL composition of the murine retina, compare it to our Cerkl -/- model, and finally assess new possible CERKL substrates by phosphorus quantification and protein-lipid overlay. Our results showed a consistent and notable decrease of the retinal SPL content (mainly ranging from 30% to 60%) in the Cerkl -/- compared to WT retinas, which was particularly evident in the glucosyl/galactosyl ceramide species (Glc/GalCer) whereas the phospholipids and neutral lipids remained unaltered. Moreover, evidence in favor of CERKL binding to GlcCer, GalCer and sphingomyelin has been gathered. Altogether, these results highlight the involvement of CERKL in the SPL metabolism, question its role as a kinase, and open new scenarios concerning its function.
AuthorsAlejandro Garanto, Nawajes A Mandal, Meritxell Egido-Gabás, Gemma Marfany, Gemma Fabriàs, Robert E Anderson, Josefina Casas, Roser Gonzàlez-Duarte
JournalExperimental eye research (Exp Eye Res) Vol. 110 Pg. 96-106 (May 2013) ISSN: 1096-0007 [Electronic] England
PMID23501591 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 Elsevier Ltd. All rights reserved.
Chemical References
  • Ceramides
  • Glycosphingolipids
  • Phospholipids
  • Sphingolipids
  • Sphingomyelins
  • dihydroceramide
  • RNA
  • Phosphotransferases (Alcohol Group Acceptor)
  • CerkL protein, mouse
  • Sphingosine
Topics
  • Animals
  • Ceramides (metabolism)
  • Chromatography, High Pressure Liquid
  • Glycosphingolipids (metabolism)
  • HEK293 Cells
  • Humans
  • Lipid Metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phospholipids (metabolism)
  • Phosphotransferases (Alcohol Group Acceptor) (physiology)
  • RNA (isolation & purification)
  • Real-Time Polymerase Chain Reaction
  • Retina (metabolism)
  • Retinitis Pigmentosa (metabolism)
  • Spectrometry, Mass, Electrospray Ionization
  • Sphingolipids (metabolism)
  • Sphingomyelins (metabolism)
  • Sphingosine (metabolism)
  • Transfection

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: