Fatty acid uptake in diabetic rat adipocytes

Heather Fraser1, Scott M. Coles2, Judith K. Woodford3, Audrey A. Frolov4, Eric J. Murphy4, Friedhelm Schroeder4, David A. Bernlohr5, Vernon Grund6
1Department of Pharmacology, University of Alberta, Edmonton, Canada
2The Cleveland Clinic Foundation, Cleveland, USA
3The Andrew Jergens Co., Cincinnati, USA
4Department of Physiology and Pharmacology, Texas A and M University, TVMC, College Station, USA
5Department of Biochemistry, University of Minnesota, Saint Paul, USA
6Department of Pharmaceutical Sciences, School of Pharmacy and Allied Health Sciences, University of Montana, Missoula, USA

Tóm tắt

The effect of diabetic status and insulin on adipocyte plasma membrane properties and fatty acid uptake was examined. Studies with inhibitors and isolated adipocyte ghost plasma membranes indicated 9Z, 11E, 13E, 15Z-octatetraenoic acid (cis-parinaric acid) uptake was protein mediated. Cis-parinaric acid uptake was inhibited by trypsin treatment or incubation with phloretin, and competed with stearic acid. The initial rate, but not maximal uptake, of cis-parinaric acid uptake was enhanced two-fold in adipocytes from diabetic rats. Concomitantly, the structure and lipid composition of adipocyte ghost membranes was dramatically altered. However, the increased initial rate of cis-parinaric acid uptake in the diabetic adipocytes was not explained by membrane alterations or by a two-fold decrease in cytosolic adipocyte fatty acid binding protein (ALBP), unless ALBP stimulated fatty acid efflux. Thus, diabetic status dramatically altered adipocyte fatty acid uptake, plasma membrane structu re, lipid composition, and cytosolic fatty acid binding protein. (Mol Cell Biochem 167: 51-60, 1997)

Từ khóa


Tài liệu tham khảo

Abumrad NA, Perkins RC, Park JH, Park CR: Mechanism of long chain fatty acid permeation in the isolated adipocyte. J Biol Chem 256: 9183–9191, 1981

Abumrad NA, Park JH, Park CR: Permeation of long-chain fatty acid into adipocytes. Kinetics, specificity, and evidence for involvement of a membrane protein. J Biol Chem 259: 8945–8953, 1984

Abumrad NA, Melki SA, Harmon CM: Transport of fatty acid in the isolated rat adipocyte and in differentiating preadipose cells. Biochem Soc Trans 18: 1130–1132, 1990

Prows DR, Jefferson JR, Incerpi S, Heyliger CE, Hertelendy ZI, Schroeder F: Arch Biochem Biophys, submitted 1995

Trigatti BL, Mangroo D, Gerber GE: Photoaffinity labelling and fatty acid permeation in 3T3-L1 adipocytes. J Biol Chem 266: 22621–22625, 1991

Abumrad NA, Forest CC, Regen DM, Sanders S: Increase in membrane uptake of long-chain fatty acids early during preadipocyte differentiation. Proc Natl Acad Sci USA 88: 6008–6012, 1991

Schroeder F, Jefferson JR, Powell D, Incerpi S, Woodford JK, Colles S, Myers-Payne S, Emge T, Hubbell T, Moncecchi D, Prows D, Heyliger CE: Expression of rat L-FABP in mouse fibroblasts: role in fat absorption. Mol Cell Biochem 123: 73–83, 1993

Harmon CM, Luce P, Beth AH, Abumrad NA: Labeling of adipocyte membranes by sulfo-N-succinimidyl derivatives of long-chain fatty acids: inhibition of fatty acid transport. J Memb Biol 121: 261–268, 1991

Waggoner DA, Bernlohr DA: In situ labeling of the adipocyte lipid binding protein with 3-[125] iodo-4-azido-N-hexadecylsalicylamide. Evidence for a role of fatty acid binding proteins in lipid uptake. J Biol Chem 265: 11417–11420, 1990

Buelt MK, Xu Z, Banaszak L, Bernlohr DA: Structural and functional characterization of the phosphorylated adipocyte lipid-binding protein (pp15). Biochemistry 31: 3493–3499, 1992

Abumrad NA, Perry PR, Whitesell RR: Stimulation by epinephrine of the membrane transport of long chain fatty acid in the adipocyte. J Biol Chem 260: 9969–9971, 1985

Abumrad NA, Perry PR, Whitesell RR: Insulin antagonizes epinephrine activation of the membrane transport of fatty acids. J Biol Chem 261: 2999–3001, 1985

Schroeder F: Hormonal effects on fatty acid binding and physical properties of rat liver plasma membranes. J Memb Biol 68: 1–10, 1982

Ramsammy LS, Boos C, Josepovitz C, Kaloyanides GJ: Biophysical and biochemical alteration of renal cortical membranes in diabetic rat. Biochim et Biophys Acta 1146: 1–8, 1993

Kamada T, Otsuji S: Lower levels of erythrocyte membrane fluidity in diabetic patients. Diabetes 32: 585–591, 1983

Zhou SL, Stump D, Sorrentino D, Potter BJ, Berk PD: Adipocyte differentiation of 3T3-L1 cells involves augmented expression of a 43-kDa plasma membrane fatty acid binding protein. J Biol Chem 267: 14456–14461, 1992

Sams GH, Hargis BM, Hargis PS: Isolation and characterization of a fatty acid binding protein in adipose tissue of Gallus Domesticus. Comp Biochem Physiol 96B: 585–590, 1990

Hresko RC, Bernier M, Hoffman RD, Flores-Riveros JR, Liao K, Laird DM, Lane MD: Identification of phosphorylated 422(aP2) protein as pp15, the 15-kilodalton target of the insulin receptor tyrosine kinase in 3T3-4 adipocytes. Proc Natl Acad Sci USA 85: 8835–8839, 1988

Melki SA, Abumrad NA: Expression of adipocyte fatty acid binding protein in streptozotocin diabetes: effects of insulin deficiency and supplementation. J Lipid Res 34: 1527–1534, 1993

Rodbell M: Metabolism of isolated fat cells. Preparation of ‘ghosts’ and their properties, adenyl cyclase and other enzymes. J Biol Chem 242: 5744–5750, 1967.

Grund VR, Goldberg ND, Hunninghake DB: Histamine receptors in adipose tissue: involvement of cyclic adenosine monophosphate and H2 receptors in the lipolytic response to histamine in the isolated canine fat cell. J Pharmacol Exp Ther 195: 176–184, 1975

Prows DR, Murphy EJ, Schroeder F: Intestinal and liver fatty acid binding proteins differentially affect fatty acid uptake and esterification in L-cells. Lipids 30: 907–910, 1995

Nemecz G, Schroeder F: Time-resolved fluorescence investigation of membrane cholesterol heterogeneity and exchange. Biochemistry 27: 7740–7749, 1988

Prows DR, Jefferson JR, Incerpi S, Heyliger CE, Hertelendy ZI, Murphy E, Schroeder F: Cis-parinaric acid uptake in L-cell fibroblasts: Hormone effects. FASEB J 7: A385, 1993

Prows DR, Jefferson JR, Murphy EJ, Incerpi S, Hertelendy ZI, Heyliger CE, Schroeder F: Cis-parinaric acid uptake in L-cells. Arch Biochem Biophys, submitted 1996

Murphy EJ, Prows DR, Jefferson JR, Schroeder F: Liver fatty acid binding protein expression in transfected fibroblasts stimulates fatty acid uptake and metabolism. Biochim Biophys Acta, in press, 1996

Schroeder F, Holland JF, Vagelos PR: Use of ßb-parinaric acid, a novel fluorimetric probe, to determine characteristic temperatures of membranes and membrane lipids from cultured animal cells. J Biol Chem 251: 6739–6746, 1976

Nemecz G, Hubbell T, Jefferson JR, Lowe JB, Schroeder F: Interaction of fatty acids with recombinant rat intestinal and liver fatty acid-bind-ing proteins. Arch Biochem Biophys 286: 300–309, 1991

Nemecz G, Jefferson JR, Schroeder F: Polyene fatty acid interactions with recombinant intestinal and liver fatty acid-binding proteins. Spectroscopic studies. J Biol Chem 266: 17112–17123, 1991

Stremmel W, Berk PD: Hepatocellular influx of [14C]oleate reflects mem-brane transport rather than intracellular metabolism or binding. Proc Natl Acad Sci USA 83: 3086–3090, 1986

Spector AA, Steinberg D, Tanaka A: Uptake of free fatty acids by Ehrlich ascites tumor cells. J Biol Chem 240: 1032–1041, 1965

Heyliger CR, Khesghi T, Murphy EJ, Schroder F: Molec Cell Biochem in press, 1996

Woodford JK, Jefferson JR, Wood WG, Hubbell T, Schroeder F: Expression of liver fatty acid binding protein alters plasma membrane lipid composition and structure in transfected L-cell fibroblasts. Biochim Biophys Acta 1145: 257–265, 1993

Jefferson JR, Powell DP, Rymaszewski Z, Kukowska-Latallo J, Lowe JB, Schroeder F: Altered membrane structure in transfected mouse L-cell fibroblasts expressing rat liver fatty acid binding protein. J Biol Chem 265: 11062–11068, 1990

Nasser K, Cheng S, Levy D: The effect of diabetes on hepatocyte plasma membrane fluidity and concanavalin A-induced agglutination. Exptl Cell Res 132: 99–104, 1981

Zannoni C, Arcioni A, Cavortata P: Fluorescence depolarization in liquid crystals and membrane bilayers. Chem Phys Lipid 32: 179–250, 1983

Schroeder F, Colles S, Kreishmann GP, Heyliger CE, Wood WG: Synaptic plasma membrane structure and polarity of long sleep and short sleep mice. Arch Biochem Biophys 309: 369–376, 1993

Matarese V, Bemlohr DA: Purification of murine adipocyte lipid binding protein. J Biol Chem 263: 14544–14551, 1988

Baxa CA, Sha RS, Buelt MK, Smith AJ, Matarese V, Chinander LL, Boundy KL, Bernlohr DA: Human adipocyte lipid binding protein: purification of the protein and cloning of its cDNA. Biochemistry 28: 8683–8690

Matarese V, Bernlohr DA: Purification of murine adipocyte lipid-binding protein. Characterization as a fatty acid-and retinoic acid-binding protein. J Biol Chem 263: 14544–14551, 1988

Lalonde JM, Levenson MA, Roe JJ, Bernlohr DA, Banaszak LJ: Adipocyte lipid-binding protein complexed arachidonic acid: titration calorimetry and x-ray crystallographic studies. J Biol Chem 269: 25339–25347, 1994

Bailey IA, Garratt CJ, Wallace SM: An effect of fluorescent probes and of insulin on the structure of adipocyte membranes. Biochem Soc Trans 6: 302–304, 1978

Dutta-Roy A, Ray TK, Sinha AK: Control of erythrocyte membrane microviscosity by insulin. Biochim Biophys Acta 816: 187–190

Bryszewska M, Leyko W: Effect of insulin on human erythrocyte membrane fluidity in diabetes mellitus. Diabetologia 24: 311–313, 1983

Juhan-Vague I, Rahmani-Jourdheuil D, Mishal Z, Roul C, Mourayre Y, Aillaud MF, Vague P: Correction by insulin added in vitro of abnormal membrane fluidity of erythrocytes from Type I (insulin dependent) diabetic patients. Diabetologia 29: 417–420, 1986

Luly P, Shinitzky M: Gross structural changes in isolated liver cell plasma membranes upon binding of insulin. Biochemistry 18: 445–450, 1979

Kamada T, McMillan DE, Yamashita T, Otsuji S: Lowered membrane fluidity of younger erythrocytes in diabetes. Diabetes Res And Clin Pract 16: 1–6, 1992

Baba Y, Kai M, Kamada T, Setoyama S, Otsuji S: Higher levels of erythrocyte membrane microviscosity in diabetes. Diabetes 28: 1138–1140, 1979

Bryszewska M, Watala C, Torzecka W: Changes in fluidity and composition of erythrocyte membranes and in composition of plasma lipids in Type I diabetes. Brit J Haematol 62: 111–116, 1986

Kamada T, Otsuji S: Lower levels of erythrocyte membrane fluidity in diabetic patients. A spin label study. Diabetes 32: 585–591, 1983

Hill MA, Court JM: Erythrocyte membrane fluidity in type 1 diabetes mellitus. Pathology 15: 449–551, 1983

Ho M-T, Massey JB, Pownall HJ, Anderson RE, Hollyfield JG: Mechanism of vitamin A movement between rod outer segment, interphotoreceptor retinoid binding protein, and liposomes. J Biol Chem 264: 928–935