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Sökning: WFRF:(Chroni Christina) > (2015) > Lipoprotein profile...

Lipoprotein profiles in human heterozygote carriers of a functional mutation P297S in scavenger receptor class B1.

Ljunggren, Stefan A (författare)
Linköpings universitet,Avdelningen för neuro- och inflammationsvetenskap,Medicinska fakulteten
Levels, Johannes H M (författare)
Academic Medical Centre, Amsterdam, the Netherlands
Hovingh, Kees (författare)
Academic Medical Centre, Amsterdam, the Netherlands
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Holleboom, Adriaan G (författare)
Academic Medical Centre, Amsterdam, the Netherlands
Vergeer, Menno (författare)
Academic Medical Centre, Amsterdam, the Netherlands
Argyri, Letta (författare)
National Center for Scientific Research "Demokritos", Athens, Greece
Gkolfinopoulou, Christina (författare)
National Center for Scientific Research "Demokritos", Athens, Greece
Chroni, Angeliki (författare)
National Center for Scientific Research "Demokritos", Athens, Greece
Sierts, Jeroen A (författare)
Academic Medical Centre, Amsterdam, the Netherlands
Kastelein, John J (författare)
Academic Medical Centre, Amsterdam, the Netherlands
Kuivenhoven, Jan Albert (författare)
University of Groningen, University Medical Center Groningen, Groningen, the Netherlands
Lindahl, Mats (författare)
Linköpings universitet,Avdelningen för neuro- och inflammationsvetenskap,Medicinska fakulteten
Karlsson, Helen (författare)
Linköpings universitet,Avdelningen för neuro- och inflammationsvetenskap,Medicinska fakulteten,Region Östergötland, Arbets- och miljömedicin
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 (creator_code:org_t)
Elsevier, 2015
2015
Engelska.
Ingår i: Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids. - : Elsevier. - 1388-1981 .- 1879-2618. ; 1851:12, s. 1587-1595
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The scavenger receptor class B type 1 (SR-B1) is an important HDL receptor involved in cholesterol uptake and efflux, but its physiological role in human lipoprotein metabolism is not fully understood. Heterozygous carriers of the SR-B1P297S mutation are characterized by increased HDL cholesterol levels, impaired cholesterol efflux from macrophages and attenuated adrenal function. Here, the composition and function of lipoproteins were studied in SR-B1P297S heterozygotes.Lipoproteins from six SR-B1P297S carriers and six family controls were investigated. HDL and LDL/VLDL were isolated by ultracentrifugation and proteins were separated by two-dimensional gel electrophoresis and identified by mass spectrometry. HDL antioxidant properties, paraoxonase 1 activities, apoA-I methionine oxidations and HDL cholesterol efflux capacity were assessed.Multivariate modeling separated carriers from controls based on lipoprotein composition. Protein analyses showed a significant enrichment of apoE in LDL/VLDL and of apoL-1 in HDL from heterozygotes compared to controls. The relative distribution of plasma apoE was increased in LDL and in lipid-free form. There were no significant differences in paraoxonase 1 activities, HDL antioxidant properties or HDL cholesterol efflux capacity but heterozygotes showed a significant increase of oxidized methionines in apoA-I.The SR-B1P297S mutation affects both HDL and LDL/VLDL protein compositions. The increase of apoE in carriers suggests a compensatory mechanism for attenuated SR-B1 mediated cholesterol uptake by HDL. Increased methionine oxidation may affect HDL function by reducing apoA-I binding to its targets. The results illustrate the complexity of lipoprotein metabolism that has to be taken into account in future therapeutic strategies aiming at targeting SR-B1.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

ApoE; ApoL-1; HDL; LDL/VLDL; P297S; SR-B1

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