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Non-vesicular trafficking by a ceramide-1-phosphate transfer protein regulates eicosanoids.

Nature | 2013

Phosphorylated sphingolipids ceramide-1-phosphate (C1P) and sphingosine-1-phosphate (S1P) have emerged as key regulators of cell growth, survival, migration and inflammation. C1P produced by ceramide kinase is an activator of group IVA cytosolic phospholipase A2α (cPLA2α), the rate-limiting releaser of arachidonic acid used for pro-inflammatory eicosanoid production, which contributes to disease pathogenesis in asthma or airway hyper-responsiveness, cancer, atherosclerosis and thrombosis. To modulate eicosanoid action and avoid the damaging effects of chronic inflammation, cells require efficient targeting, trafficking and presentation of C1P to specific cellular sites. Vesicular trafficking is likely but non-vesicular mechanisms for C1P sensing, transfer and presentation remain unexplored. Moreover, the molecular basis for selective recognition and binding among signalling lipids with phosphate headgroups, namely C1P, phosphatidic acid or their lyso-derivatives, remains unclear. Here, a ubiquitously expressed lipid transfer protein, human GLTPD1, named here CPTP, is shown to specifically transfer C1P between membranes. Crystal structures establish C1P binding through a novel surface-localized, phosphate headgroup recognition centre connected to an interior hydrophobic pocket that adaptively expands to ensheath differing-length lipid chains using a cleft-like gating mechanism. The two-layer, α-helically-dominated 'sandwich' topology identifies CPTP as the prototype for a new glycolipid transfer protein fold subfamily. CPTP resides in the cell cytosol but associates with the trans-Golgi network, nucleus and plasma membrane. RNA interference-induced CPTP depletion elevates C1P steady-state levels and alters Golgi cisternae stack morphology. The resulting C1P decrease in plasma membranes and increase in the Golgi complex stimulates cPLA2α release of arachidonic acid, triggering pro-inflammatory eicosanoid generation.

Pubmed ID: 23863933 RIS Download

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Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: GM072754
  • Agency: PHS HHS, United States
    Id: T32 008695
  • Agency: BLRD VA, United States
    Id: I01 BX001792
  • Agency: NCI NIH HHS, United States
    Id: CA121493
  • Agency: NCI NIH HHS, United States
    Id: R01 CA154314
  • Agency: NCI NIH HHS, United States
    Id: P30 CA008748
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM072754
  • Agency: NCI NIH HHS, United States
    Id: CA154314
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL072925
  • Agency: NCI NIH HHS, United States
    Id: R01 CA121493
  • Agency: NIH HHS, United States
    Id: S10 OD010641
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM045928
  • Agency: NIGMS NIH HHS, United States
    Id: GM45928

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