Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5509057 | Biochimie | 2016 | 26 Pages |
Abstract
The review summarizes recent findings on the regulation of sphingolipid catabolism and cholesterol secretion from the endosomal compartment by lipid modifiers, an essential stimulation by anionic membrane lipids and an inhibition of crucial steps by cholesterol and SM. Reconstitution experiments in the presence of all proteins needed, hydrolase and activator proteins, reveal an up to 10-fold increase of ganglioside catabolism just by the incorporation of anionic lipids into the ganglioside carrying membranes, whereas an additional incorporation of cholesterol inhibits GM2 catabolism substantially. It is suggested that lipid and other low molecular modifiers affect the genotype-phenotype relationship observed in patients with lysosomal diseases.
Keywords
NPC1GM2 activator proteinHexosaminidase ASphingolipid activator proteinGM2APHexAglycosphingolipidGSLNBDDOPCNPC2ESCRTNPCASM7-nitrobenz-2-oxa-1,3-diazol-4-ylacid sphingomyelinasesphingomyelinphosphatidic acidNiemann-Pick disease type CLTPcationic amphiphilic drugSAPCADPlasma membranephosphatidylcholinephosphatidylglycerolendosomal sorting complexes required for transportBMPlipid transfer protein
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Authors
Konrad Sandhoff,