| Literature DB >> 30808683 |
Lita A Freeman1, Robert D Shamburek2, Maureen L Sampson3, Edward B Neufeld4, Masaki Sato4, Sotirios K Karathanasis5, Alan T Remaley6.
Abstract
Familial LCAT deficiency (FLD) patients accumulate lipoprotein-X (LP-X), an abnormal nephrotoxic lipoprotein enriched in free cholesterol (FC). The low neutral lipid content of LP-X limits the ability to detect it after separation by lipoprotein electrophoresis and staining with Sudan Black or other neutral lipid stains. A sensitive and accurate method for quantitating LP-X would be useful to examine the relationship between plasma LP-X and renal disease progression in FLD patients and could also serve as a biomarker for monitoring recombinant human LCAT (rhLCAT) therapy. Plasma lipoproteins were separated by agarose gel electrophoresis and cathodal migrating bands corresponding to LP-X were quantified after staining with filipin, which fluoresces with FC, but not with neutral lipids. rhLCAT was incubated with FLD plasma and lipoproteins and LP-X changes were analyzed by agarose gel electrophoresis. Filipin detects synthetic LP-X quantitatively (linearity 20-200 mg/dl FC; coefficient of variation <20%) and sensitively (lower limit of quantitation <1 mg/ml FC), enabling LP-X detection in FLD, cholestatic, and even fish-eye disease patients. rhLCAT incubation with FLD plasma ex vivo reduced LP-X dose dependently, generated HDL, and decreased lipoprotein FC content. Filipin staining after agarose gel electrophoresis sensitively detects LP-X in human plasma and accurately quantifies LP-X reduction after rhLCAT incubation ex vivo.Entities:
Keywords: cholesterol; familial lecithin:cholesterol acyltransferase deficiency; fish-eye disease; high density lipoprotein; kidney; lecithin:cholesterol acyltransferase; phospholipids
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Year: 2019 PMID: 30808683 PMCID: PMC6495165 DOI: 10.1194/jlr.D090233
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922