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A proteomic study of the apolipoproteins in LDL subclasses in patients with the metabolic syndrome and type 2 diabetes

Davidsson, P. (author)
Hulthe, Johannes, 1970 (author)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Wallenberg Laboratory
Fagerberg, Björn, 1943 (author)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Institutionen för invärtesmedicin, Avdelningen för internmedicin,Wallenberg Laboratory,Institute of Internal Medicine, Dept of Medicine
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Olsson, B. M. (author)
Hallberg, C. (author)
Dahllof, B. (author)
Camejo, German, 1936 (author)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Wallenberg Laboratory
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 (creator_code:org_t)
2005
2005
English.
In: J Lipid Res. - 0022-2275. ; 46:9, s. 1999-2006
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The exchangeable apolipoproteins present in small, dense LDL (sdLDL) and large, buoyant LDL subclasses were evaluated with a quantitative proteomic approach in patients with the metabolic syndrome and with type 2 diabetes, both with subclinical atherosclerosis and the B LDL phenotype. The analyses included surface-enhanced laser adsorption/ionization, time-of-flight mass spectrometry, and subsequent identification by mass spectrometry or immunoblotting and were carried out in LDL subclasses isolated by ultracentrifugation in deuterium oxide gradients with near physiological salt concentrations. The sdLDLs of both types of patients were enriched in apolipoprotein C-III (apoC-III) and were depleted of apoC-I, apoA-I, and apoE compared with matched healthy controls with the A phenotype. The LDL complexes formed in serum from patients with diabetes with the arterial proteoglycan (PG) versican were also enriched in apoC-III. In addition, there was a significant correlation between the apoC-III content in sdLDL in patients and the apparent affinity of their LDLs for arterial versican. The unique distribution of exchangeable apolipoproteins in the sdLDLs of the patients studied, especially high apoC-III, coupled with the augmented affinity with arterial PGs, may contribute to the strong association of the dyslipidemia of insulin resistance with increased risk for cardiovascular disease.

Keyword

Animals
Apolipoprotein C-III
Apolipoproteins/*blood
Apolipoproteins C/blood
Arteries/chemistry
Diabetes Mellitus
Type 2/*blood
Humans
Lectins
C-Type
Lipoproteins
LDL/*blood/isolation & purification/metabolism
Male
Metabolic Syndrome X/*blood
Middle Aged
Protein Array Analysis
Proteochondroitin Sulfates/metabolism
Proteoglycans/metabolism
*Proteomics
Swine
Versicans

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