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Expression of rat L-FABP in mouse fibroblasts: role in fat absorption
Authors:F Schroeder  J R Jefferson  D Powell  S Incerpi  J K Woodford  S M Colles  S Myers-Payne  T Emge  T Hubbell  D Moncecchi  D R Prows  C E Heyliger
Institution:(1) Divi of Pharmacology & Med. Chem., Dept. of Pharmacology & Cell Biophysics, University of Cincinnati Medical Center, ML004, 45267-0004 Cincinnati, OH, USA;(2) Dept. of Chemistry, University of Cincinnati, 45267-0172 Cincinnati, OH, USA;(3) Dept. of Chemistry, Luther College, 52101-1045 Decorah, IA, USA;(4) Dipartimento Di Biologia, Universita Degli Studi Di Roma, Tor Vergata, Rome, Italy
Abstract:Fatty acid-binding proteins (FABP) are abundant cytosolic proteins whose level is responsive to nutritional, endocrine, and a variety of pathological states. Although FABPs have been investigatedin vitro for several decades, little is known of their physiological function. Liver L-FABP binds both fatty acids and cholesterol. Competitive binding analysis and molecular modeling studies of L-FABP indicate the presence of two ligand binding pockets that accomodate one fatty acid each. One fatty acid binding site is identical to the cholesterol binding site. To test whether these observations obtainedin vitro were physiologically relevant, the cDNA encoding L-FABP was transfected into L-cells, a cell line with very low endogenous FABP and sterol carrier proteins. Uptake of both ligands did not differ between control cells and low expression clones. In contrast, both fatty acid uptake and cholesterol uptake were stimulated in the high expression cells. In high expression cells, uptake of fluorescent cis-parinaric acid was enhanced more than that of trans-parinaric acid. This is consistent with the preferential binding of cis-fatty acids to L-FABP but in contrast to the preferential binding of trans-parinaric acid to the L-cell plasma membrane fatty acid transporter (PMFABP). These data show that the level of cytosolic fatty acids in intact cells can regulate both the extent and specificity of fatty acid uptake. Last, sphingomyelinase treatment of L-cells released cholesterol from the plasma membrane to the cytoplasm and stimulated microsomal acyl-CoA: cholesteryl acyl transferase (ACAT). This process was accelerated in high expression cells. These observations show for the first time in intact cells that L-FABP, a protein most prevalent in liver and intestine where much fat absorption takes place, may have a role in fatty acid and cholesterol absorption.Abbreviations FABP fatty acid-binding protein - L-FABP liver fatty acid-binding protein - I-FABP intestinal fatty acid-binding protein - H-FABP heart fatty acid-binding protein - A-FABP adipocyte fatty acid-binding protein - PMFABP plasma membrane fatty acid-binding protein - SCP-2 sterol carrier protein-2 - Dehydroergosterol (DHE) d-5,7,9(11),22-ergostatetraene-3b-ol - cis-parinaric acid-9Z, 11E, 13E, 15Z-octatetraenoic acid - trans parinaric acid, 9E, 11E, 13E, 14E-octatetraenoic acid - BSA bovine serum albumin - KRH Krebs-Ringer-Henseleit buffer
Keywords:liver  fatty acid-binding protein  sterol binding protein  L-cells  fat  cholesterol  dehydroergosterol  fatty acid  cis-parinaric acid  transport  insulin  epinephrine  fluorescence
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