Matches in SemOpenAlex for { <https://semopenalex.org/work/W2788216507> ?p ?o ?g. }
- W2788216507 endingPage "783" @default.
- W2788216507 startingPage "773" @default.
- W2788216507 abstract "•ANGPTL4 mRNA is highest in the subcutaneous adipose tissue of obese individuals. •ANGPTL4 and LPL mRNA levels positively associate in multiple adipose tissue depots. •ANGPTL4 and LPL protein levels negatively associate in subcutaneous adipose tissue. •Adipose tissue ANGPTL4 mRNA levels are higher in the fasted than the postprandial state. Background Elevated plasma triglycerides are increasingly viewed as a causal risk factor for coronary artery disease. One protein that raises plasma triglyceride levels and that has emerged as a modulator of coronary artery disease risk is angiopoietin-like 4 (ANGPTL4). ANGPTL4 raises plasma triglyceride levels by inhibiting lipoprotein lipase (LPL), the enzyme that catalyzes the hydrolysis of circulating triglycerides on the capillary endothelium. Objective The objective of the present study was to assess the association between ANGPTL4 and LPL in human adipose tissue, and to examine the influence of nutritional status on ANGPTL4 expression. Methods We determined ANGPTL4 and LPL mRNA and protein levels in different adipose tissue depots in a large number of severely obese patients who underwent bariatric surgery. Furthermore, in 72 abdominally obese subjects, we measured ANGPTL4 and LPL mRNA levels in subcutaneous adipose tissue in the fasted and postprandial state. Results ANGPTL4 mRNA levels were highest in subcutaneous adipose tissue, whereas LPL mRNA levels were highest in mesenteric adipose tissue. ANGPTL4 and LPL mRNA levels were strongly positively correlated in the omental and subcutaneous adipose tissue depots. In contrast, ANGPTL4 and LPL protein levels were negatively correlated in subcutaneous adipose tissue, suggesting a suppressive effect of ANGPTL4 on LPL protein abundance in subcutaneous adipose tissue. ANGPTL4 mRNA levels were 38% higher in the fasted compared to the postprandial state. Conclusion Our data provide valuable insights into the relationship between ANGPTL4 and LPL in human adipose tissue, as well as the physiological function and regulation of ANGPTL4 in humans. Elevated plasma triglycerides are increasingly viewed as a causal risk factor for coronary artery disease. One protein that raises plasma triglyceride levels and that has emerged as a modulator of coronary artery disease risk is angiopoietin-like 4 (ANGPTL4). ANGPTL4 raises plasma triglyceride levels by inhibiting lipoprotein lipase (LPL), the enzyme that catalyzes the hydrolysis of circulating triglycerides on the capillary endothelium. The objective of the present study was to assess the association between ANGPTL4 and LPL in human adipose tissue, and to examine the influence of nutritional status on ANGPTL4 expression. We determined ANGPTL4 and LPL mRNA and protein levels in different adipose tissue depots in a large number of severely obese patients who underwent bariatric surgery. Furthermore, in 72 abdominally obese subjects, we measured ANGPTL4 and LPL mRNA levels in subcutaneous adipose tissue in the fasted and postprandial state. ANGPTL4 mRNA levels were highest in subcutaneous adipose tissue, whereas LPL mRNA levels were highest in mesenteric adipose tissue. ANGPTL4 and LPL mRNA levels were strongly positively correlated in the omental and subcutaneous adipose tissue depots. In contrast, ANGPTL4 and LPL protein levels were negatively correlated in subcutaneous adipose tissue, suggesting a suppressive effect of ANGPTL4 on LPL protein abundance in subcutaneous adipose tissue. ANGPTL4 mRNA levels were 38% higher in the fasted compared to the postprandial state. Our data provide valuable insights into the relationship between ANGPTL4 and LPL in human adipose tissue, as well as the physiological function and regulation of ANGPTL4 in humans." @default.
- W2788216507 created "2018-03-06" @default.
- W2788216507 creator A5028342693 @default.
- W2788216507 creator A5036550676 @default.
- W2788216507 creator A5038344046 @default.
- W2788216507 creator A5049635388 @default.
- W2788216507 creator A5063605678 @default.
- W2788216507 creator A5067125694 @default.
- W2788216507 date "2018-05-01" @default.
- W2788216507 modified "2023-10-18" @default.
- W2788216507 title "Regulation of angiopoietin-like 4 and lipoprotein lipase in human adipose tissue" @default.
- W2788216507 cites W1067311966 @default.
- W2788216507 cites W1524646539 @default.
- W2788216507 cites W1651622892 @default.
- W2788216507 cites W1672804368 @default.
- W2788216507 cites W1871647034 @default.
- W2788216507 cites W2008962463 @default.
- W2788216507 cites W2014593901 @default.
- W2788216507 cites W2018602526 @default.
- W2788216507 cites W2026370027 @default.
- W2788216507 cites W2028558940 @default.
- W2788216507 cites W2032290459 @default.
- W2788216507 cites W2032876806 @default.
- W2788216507 cites W2035216298 @default.
- W2788216507 cites W2036747551 @default.
- W2788216507 cites W2038706336 @default.
- W2788216507 cites W2045632404 @default.
- W2788216507 cites W2066836273 @default.
- W2788216507 cites W2075248264 @default.
- W2788216507 cites W2078778450 @default.
- W2788216507 cites W2093583036 @default.
- W2788216507 cites W2095786854 @default.
- W2788216507 cites W2102892430 @default.
- W2788216507 cites W2109284620 @default.
- W2788216507 cites W2113574122 @default.
- W2788216507 cites W2115509231 @default.
- W2788216507 cites W2116671187 @default.
- W2788216507 cites W2119240544 @default.
- W2788216507 cites W2123926879 @default.
- W2788216507 cites W2129606778 @default.
- W2788216507 cites W2129937334 @default.
- W2788216507 cites W2132116144 @default.
- W2788216507 cites W2141143799 @default.
- W2788216507 cites W2141428393 @default.
- W2788216507 cites W2162789070 @default.
- W2788216507 cites W2163838850 @default.
- W2788216507 cites W2167704203 @default.
- W2788216507 cites W2196793559 @default.
- W2788216507 cites W2294822677 @default.
- W2788216507 cites W2323589075 @default.
- W2788216507 cites W2331756138 @default.
- W2788216507 cites W2339363450 @default.
- W2788216507 cites W2526340886 @default.
- W2788216507 cites W2617605538 @default.
- W2788216507 cites W2618984243 @default.
- W2788216507 cites W2697923644 @default.
- W2788216507 doi "https://doi.org/10.1016/j.jacl.2018.02.006" @default.
- W2788216507 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29555209" @default.
- W2788216507 hasPublicationYear "2018" @default.
- W2788216507 type Work @default.
- W2788216507 sameAs 2788216507 @default.
- W2788216507 citedByCount "22" @default.
- W2788216507 countsByYear W27882165072018 @default.
- W2788216507 countsByYear W27882165072019 @default.
- W2788216507 countsByYear W27882165072020 @default.
- W2788216507 countsByYear W27882165072021 @default.
- W2788216507 countsByYear W27882165072022 @default.
- W2788216507 countsByYear W27882165072023 @default.
- W2788216507 crossrefType "journal-article" @default.
- W2788216507 hasAuthorship W2788216507A5028342693 @default.
- W2788216507 hasAuthorship W2788216507A5036550676 @default.
- W2788216507 hasAuthorship W2788216507A5038344046 @default.
- W2788216507 hasAuthorship W2788216507A5049635388 @default.
- W2788216507 hasAuthorship W2788216507A5063605678 @default.
- W2788216507 hasAuthorship W2788216507A5067125694 @default.
- W2788216507 hasConcept C104317684 @default.
- W2788216507 hasConcept C126322002 @default.
- W2788216507 hasConcept C134018914 @default.
- W2788216507 hasConcept C167734588 @default.
- W2788216507 hasConcept C171089720 @default.
- W2788216507 hasConcept C2777025900 @default.
- W2788216507 hasConcept C2778163477 @default.
- W2788216507 hasConcept C2778199505 @default.
- W2788216507 hasConcept C2778913445 @default.
- W2788216507 hasConcept C2779094623 @default.
- W2788216507 hasConcept C55493867 @default.
- W2788216507 hasConcept C555293320 @default.
- W2788216507 hasConcept C71924100 @default.
- W2788216507 hasConcept C77305985 @default.
- W2788216507 hasConcept C86803240 @default.
- W2788216507 hasConcept C94879076 @default.
- W2788216507 hasConceptScore W2788216507C104317684 @default.
- W2788216507 hasConceptScore W2788216507C126322002 @default.
- W2788216507 hasConceptScore W2788216507C134018914 @default.
- W2788216507 hasConceptScore W2788216507C167734588 @default.
- W2788216507 hasConceptScore W2788216507C171089720 @default.
- W2788216507 hasConceptScore W2788216507C2777025900 @default.
- W2788216507 hasConceptScore W2788216507C2778163477 @default.