Obesity and diabetes-related disorders have increasingly great prevalence in the western world. Coronary heart disease is the main cause of death among many populations. Due to dietary and genetic causes, atherosclerosis affects over a million people each year with cardiac manifestations. The presence of lysophosphatidylcholine and other inflammatory molecules in the atheroma have led to inquiries regarding the role of phospholipases in the development of atherosclerosis. As the number of phospholipases is large, detailing the contribution of each one is not yet complete. Recent studies have linked human polymorphisms of the group 1B phospholipase A2 gene (PLA2G1B) with increased central adiposity, which is a risk factor for cardiovascular disease. Phospholipase A2 group 1B is a digestive enzyme that aids digestion by selectively catalyzing the conversion of phospholipids in the gut lumen to lysophosphatidylcholine (LPC) and fatty acid. Mice deficient in this enzyme retain the ability to digest dietary lipids due to compensatory enzymes, but do not produce LPC to a similar extent. Furthermore, Pla2g1b-/- mice are resistant to diet-induced obesity, diet-induced type-2 diabetes, and diet-induced hyperlipidemia. The mechanism involves increased fatty acid metabolism, decreased hepatic very-low-density lipoprotein (VLDL) production, and increased post-prandial triglyceride rich lipoprotein clearance. However, the specific subcellular details of how plasma LPC alters hepatocyte metabolism are not known. Furthermore, it is not known whether genetic inhibition of Pla2g1b leads to a decreased risk of atherosclerosis in vivo. This proposal addresses these concerns by testing the ex vivo, in vitro, and in vivo effects of Pla2g1b inhibition and the addition of its enzymatic product, LPC. Mitochondria will be isolated and the effects of LPC upon membrane integrity and potential will be determined. The effect of LPC upon fatty acid metabolism in isolated hepatocytes will also be ascertained. Furthermore, the effect of Pla2g1b competence upon atherosclerosis development and systemic inflammation will be investigated in a mouse model of diet-induced atherosclerosis.

Public Health Relevance

Small variations in the digestive gene PLA2G1B have been linked with increased abdominal obesity, which is a risk factor for heart attack and stroke. Understanding this link can have potential benefit for the more than one million people per year who have heart attacks and stroke and for the millions more who have other risk factors for these diseases.

Agency
National Institute of Health (NIH)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31HL110527-03
Application #
8692585
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Meadows, Tawanna
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Cincinnati
Department
Pathology
Type
Schools of Medicine
DUNS #
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Hollie, Norris I; Konaniah, Eddy S; Goodin, Colleen et al. (2014) Group 1B phospholipase A? inactivation suppresses atherosclerosis and metabolic diseases in LDL receptor-deficient mice. Atherosclerosis 234:377-80
Hollie, Norris I; Cash, James G; Matlib, M Abdul et al. (2014) Micromolar changes in lysophosphatidylcholine concentration cause minor effects on mitochondrial permeability but major alterations in function. Biochim Biophys Acta 1841:888-95