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Lysosomal degradation of membrane lipids
Authors:Thomas Kolter
Institution: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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