Wiley Encyclopedia of Molecular Medicine 2002
DOI: 10.1002/0471203076.emm0742
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Lipoprotein Lipase

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Cited by 4 publications
(4 citation statements)
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“…Lipoprotein lipase is one of the key enzymes regulating TG and lipoprotein metabolism and is mostly found in adipose tissue and skeletal muscle (Mead et al, 2002). It has been shown that lipoprotein lipase activity in adipose tissue is higher in obese than in lean individuals at rest (Poirier & Despres, 2001) and it is also known to become metabolically active for several hours after exercise cessation (Kantor et al, 1984).…”
Section: Discussionmentioning
confidence: 99%
“…Lipoprotein lipase is one of the key enzymes regulating TG and lipoprotein metabolism and is mostly found in adipose tissue and skeletal muscle (Mead et al, 2002). It has been shown that lipoprotein lipase activity in adipose tissue is higher in obese than in lean individuals at rest (Poirier & Despres, 2001) and it is also known to become metabolically active for several hours after exercise cessation (Kantor et al, 1984).…”
Section: Discussionmentioning
confidence: 99%
“…The mature LPL protein consists of 448 amino acids with a molecular weight of 55 kDa after resecting the signal peptide (Wong & Schotz 2002). The enzyme is active as a non‐covalent homodimer and is bound to the surface of endothelial cells via glycosaminoglycans, from where it can be released by heparin (Mead, Irvine & Ramji 2002). Lipoprotein lipase plays a key role in lipid metabolism by hydrolysing triglycerides from chylomicrons and very low‐density lipoproteins (VLDL) to non‐esterified fatty acids and 2‐monoacylglycerol, which are utilized either for storage or for energy production (Wang, Hartsuck & McConathy 1992).…”
Section: Introductionmentioning
confidence: 99%
“…Lipoprotein lipase plays a key role in lipid metabolism by hydrolysing triglycerides from chylomicrons and very low‐density lipoproteins (VLDL) to non‐esterified fatty acids and 2‐monoacylglycerol, which are utilized either for storage or for energy production (Wang, Hartsuck & McConathy 1992). The abnormalities in LPL function have been found to be associated with a number of pathophysiological conditions, including atherosclerosis, chylomicronaemia, obesity, Alzheimer's disease and dyslipidaemia associated with diabetes, insulin resistance and infection (Mead et al . 2002).…”
Section: Introductionmentioning
confidence: 99%
“…Several lines of evidence (reviewed by us in [34][35][36]) have shown that the LPL expressed by macrophages is pro-atherogenic. Such an action involves both its catalytic activity and a non-catalytic bridging function that leads to the accumulation, and thereby uptake, of lipoproteins [34][35][36]. We found that TGF-β inhibits LPL mRNA expression, protein levels and enzymatic activity in a range of macrophage sources from different species, including human monocyte-derived macrophages [30].…”
Section: Molecular Mechanisms Underlying the Tgf-β-mediated Regulatiomentioning
confidence: 99%