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Lysosomal degradation of membrane lipids
Authors:Thomas Kolter
Affiliation:LiMES - Life and Medical Sciences Institute, Membrane Biology and Lipid Biochemistry Unit, c/o Kekulé-Institut für Organische Chemie und Biochemie, University of Bonn, Gerhard-Domagk Str. 1, D-53121 Bonn, Germany
Abstract:The constitutive degradation of membrane components takes place in the acidic compartments of a cell, the endosomes and lysosomes. Sites of lipid degradation are intralysosomal membranes that are formed in endosomes, where the lipid composition is adjusted for degradation. Cholesterol is sorted out of the inner membranes, their content in bis(monoacylglycero)phosphate increases, and, most likely, sphingomyelin is degraded to ceramide. Together with endosomal and lysosomal lipid-binding proteins, the Niemann-Pick disease, type C2-protein, the GM2-activator, and the saposins sap-A, -B, -C, and -D, a suitable membrane lipid composition is required for degradation of complex lipids by hydrolytic enzymes.
Keywords:BMP, bis(monoacylglycero)phosphate   ESCRT, endosomal sorting complexes required for transport   FRET, fluorescence or Fö  rster resonance energy transfer   GM1, GM2, GM3, ganglioside-nomenclature according to Svennerholm, compare Fig. 1 for structures   GSL, glycosphingolipid   LLBPs, lysosomal lipid-binding proteins   MVBs, multivesicular bodies   NBD, 4-nitrobenzo-2-oxa-1,3-diazol   NPC1, Niemann-Pick disease, type C1-protein   NPC2, Niemann-Pick disease, type C2-protein   ORP, oxysterol binding protein-related protein   PAF, platelet activating factor   PtdIns, phosphatidylinositol   sap, saposin   SAP, sphingolipid activator protein (GM2-activator, sap-A-sap-D)   SCP-2, sterol carrier protein-2   sn1, sn2, stereospecific numbering of glycerolipids according to IUPAC
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