Efficient and regulated import of long chain fatty acids (LCFAs) into specific tissues is critical for normal lipid homeostasis. Mismatch between LCFA import and utilization in the pancreas, skeletal muscle, vascular endothelial cells, and the heart may play an important role in the pathogenesis of diabetes and heart failure. When present at high, pathophysiologic concentrations, un-ionized LCFAs undergo rapid translocation from one leaflet of the bilayer to the other by a non- protein-mediated mechanism. However, evidence is emerging that proteins play an important role in the trafficking of LCFAs across the plasma membrane of cells at low, physiologic LCFA concentrations. In previous work, we identified the long-chain fatty acid transport protein (FATP1) and acyl-CoA synthetase (ACS1) as proteins that facilitate LCFA transport into cells. This project is designed to molecularly characterize FATP1 and its role in vectorial fatty acid transport across the membranes of mammalian cells. We will test the hypothesis that FATP1 functions as a component of an oligomeric complex that transports and esterifies LCFAs.
In Specific Aim 1 we will analyze structure-function correlates for FATP1.
In Specific Aim 2 we will characterize the FATP1 oligomeric complex.
In Specific Aim 3 we will evaluate the role of esterification in FATP1-mediated transport. Together these studies will help to define the molecular mechanisms by which LCFAs are transported across the plasma membrane of mammalian cells. Characterization of these mechanisms has relevance to common human diseases such as diabetes and heart failure in which abnormal lipid homeostasis contributes to pathogenesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK054268-04A1
Application #
6542781
Study Section
Metabolism Study Section (MET)
Program Officer
Haft, Carol R
Project Start
1998-09-22
Project End
2007-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
4
Fiscal Year
2002
Total Cost
$226,058
Indirect Cost
Name
Washington University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Gale, Sarah E; Westover, Emily J; Dudley, Nicole et al. (2009) Side chain oxygenated cholesterol regulates cellular cholesterol homeostasis through direct sterol-membrane interactions. J Biol Chem 284:1755-64
Richards, M Rachel; Harp, Jeffrey D; Ory, Daniel S et al. (2006) Fatty acid transport protein 1 and long-chain acyl coenzyme A synthetase 1 interact in adipocytes. J Lipid Res 47:665-72
Richards, M Rachel; Listenberger, Laura L; Kelly, Alicia A et al. (2003) Oligomerization of the murine fatty acid transport protein 1. J Biol Chem 278:10477-83
Schaffer, Jean E (2002) Fatty acid transport: the roads taken. Am J Physiol Endocrinol Metab 282:E239-46
Lewis, S E; Listenberger, L L; Ory, D S et al. (2001) Membrane topology of the murine fatty acid transport protein 1. J Biol Chem 276:37042-50
Listenberger, L L; Ory, D S; Schaffer, J E (2001) Palmitate-induced apoptosis can occur through a ceramide-independent pathway. J Biol Chem 276:14890-5
Chiu, H C; Kovacs, A; Ford, D A et al. (2001) A novel mouse model of lipotoxic cardiomyopathy. J Clin Invest 107:813-22
Gargiulo, C E; Stuhlsatz-Krouper, S M; Schaffer, J E (1999) Localization of adipocyte long-chain fatty acyl-CoA synthetase at the plasma membrane. J Lipid Res 40:881-92