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Lipoprotein size is a main determinant for the rate of hydrolysis by exogenous LPL in human plasma

Kovrov, Oleg (author)
Umeå universitet,Fysiologisk kemi
Landfors, Fredrik (author)
Umeå universitet,Avdelningen för medicin
Saar-Kovrov, Valeria (author)
Umeå universitet,Fysiologisk kemi,Department of Pathology, CARIM School for Cardiovascular Diseases MUMC+, Maastricht University, Maastricht, Netherlands
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Näslund, Ulf (author)
Umeå universitet,Avdelningen för medicin,Heart Centre
Olivecrona, Gunilla (author)
Umeå universitet,Fysiologisk kemi
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 (creator_code:org_t)
American Society for Biochemistry and Molecular Biology, 2022
2022
English.
In: Journal of Lipid Research. - : American Society for Biochemistry and Molecular Biology. - 0022-2275 .- 1539-7262. ; 63:1
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • LPL is a key player in plasma triglyceride metabolism. Consequently, LPL is regulated by several proteins during synthesis, folding, secretion, and transport to its site of action at the luminal side of capillaries, as well as during the catalytic reaction. Some proteins are well known, whereas others have been identified but are still not fully understood. We set out to study the effects of the natural variations in the plasma levels of all known LPL regulators on the activity of purified LPL added to samples of fasted plasma taken from 117 individuals. The enzymatic activity was measured at 25°C using isothermal titration calorimetry. This method allows quantification of the ability of an added fixed amount of exogenous LPL to hydrolyze triglyceride-rich lipoproteins in plasma samples by measuring the heat produced. Our results indicate that, under the conditions used, the normal variation in the endogenous levels of apolipoprotein C1, C2, and C3 or the levels of angiopoietinlike proteins 3, 4, and 8 in the fasted plasma samples had no significant effect on the recorded activity of the added LPL. Instead, the key determinant for the LPL activity was a lipid signature strongly correlated to the average size of the VLDL particles. The signature involved not only several lipoprotein and plasma lipid parameters but also apolipoprotein A5 levels. While the measurements cannot fully represent the action of LPL when attached to the capillary wall, our study provides knowledge on the interindividual variation of LPL lipolysis rates in human plasma.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Keyword

Angiopoietin-like proteins
Apolipoproteins
Capillaries
Exogenous LPL
Isothermal titration calorimetry
Lipid signature
Lipidomics
Plasma triglyceride metabolism
VLDL particle size

Publication and Content Type

ref (subject category)
art (subject category)

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