Skip to main content
Log in

Regulation of fatty acid transport and membrane transporters in health and disease

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

Long chain fatty acid uptake across the plasma membrane occurs, in part, via a protein-mediated process involving a number of fatty acid binding proteins known as fatty acid transporters. A critical step in furthering the understandings of fatty acid transport was the discovery that giant vesicles, prepared from tissues such as muscle and heart, provided a suitable system for measuring fatty acid uptake. These vesicles are large (10–15 μm diameter), are oriented fully right side out, and contain cytosolic FABP in the lumen, which acts as a fatty acid sink, while none of the fatty acid taken up is metabolized or associated with the plasma membrane. The key fatty acid transporters FAT/CD36 and FABPpm are expressed in muscle and heart and their plasma membrane content is positively correlated with rates of fatty acid transport. These transporters are regulated acutely (within minutes) and chronically (days). For instance, both muscle contraction and insulin can translocate FAT/CD36 from an intracellular pool to the plasma membrane, thereby increasing fatty acid transport. With obesity, fatty acid transport is increased along with a concomitant increase in plasmalemmal FAT/CD36 (heart, muscle) and FABPpm (heart only), but without change in the expression of these transporters. This latter observation suggests that some of the fatty acid transporters are permanently relocated to the plasma membrane. In other studies it also appears that fatty acid transport rates are altered in a reciprocal manner to glucose transport. Since disorders in lipid metabolism appear to be an important factor contributing to the etiology of a number of common human diseases such as diabetes and obesity, our evidence that protein-mediated fatty acid transport is a key step in lipid metabolism allows the speculation that malfunctioning of the fatty acid transport process could be a common critical factor in the pathogenesis of these diseases.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Abumrad NA, Harmon C, Ibrahimi A: Membrane transport of long-chain fatty acids: Evidence for a facilitated process. J Lipid Res 39: 2309–2318, 1998

    Google Scholar 

  2. Luiken JJFP, Schaap FG, van Nieuwenhoven FA, van der Vusse GJ, Bonen A, Glatz JFC: Cellular fatty acid transport in heart and muscle as facilitated by proteins. Lipids 34: S169–S175, 1999

    Google Scholar 

  3. Hamilton JA, Kamp F: How are free fatty acids transported in membranes? Is it by proteins or by free diffusion through the lipids? Diabetes 48: 2255–2269, 1999

    Google Scholar 

  4. 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

    Google Scholar 

  5. Berk PD, Zhou S-L, Kiang C-L, Stump D, Bradbury M, Isola L: Uptake of long chain fatty acids is selectively up-regulated in adipocytes of Zucker rats with genetic obesity and non-insulin-dependent diabetes mellitus. J Biol Chem 272: 8830–8835, 1997

    Google Scholar 

  6. Luiken JJFP, van Nieuwenhoven FA, America G, van der Vusse GJ, Glatz JFC: Uptake and metabolism of palmitate by isolated cardiac myocytes from adult rats: Involvement of sarcolemmal proteins. J Lipid Res 38: 725–758, 1997

    Google Scholar 

  7. King PA, Hirschman MF, Horton ED, Horton ES: Glucose transport in skeletal muscle membrane vesicles from control and exercised rats. Am J Physiol 257 (Cell Physiol): C1128–C1134, 1989

    Google Scholar 

  8. Coburn CT, Knapp FF Jr, Febbraio M, Beets AL, Silverstein RL, Abumrad NA: Defective uptake and utilization of long chain fatty acids in muscle and adipose tissue of CD36 knockout mice. J Biol Chem 275: 32523–32529, 2000

    Google Scholar 

  9. Hajri T, Ibrahimi A, Coburn CT, Knapp FF Jr, Kurtz T, Pravenec M, Abumrad NA: Defective fatty acid uptake in the spontaneously hypertensive rat is a primary determinant of altered glucose metabolism, hyperinsulinemia, and myocardial hypertrophy. J Biol Chem 276: 23661–23666, 2001

    Google Scholar 

  10. Kropp J, Eisenhut M, Ambrose KR, Knapp FF Jr, Franke WG: Pharmacokinetics and metabolism of the methyl-branched fatty acid (BMIPP) in animals and humans. J Nucl Med 40: 1484–1491, 1999

    Google Scholar 

  11. Mokler FT, Lin Q, Luo H, McPherson DW, Beets AL, Bockisch A, Kropp J, Knapp FF Jr: Dual-label studies with [125I]-3(R)/[131I]-3(S)-BMIPP show similar metabolism in rat tissues. J Nucl Med 40: 1918–1927, 1999

    Google Scholar 

  12. Lin Q, Luo H, Mokler F, Beets AL, Ambrose KR, McPherson DW, Kropp J, Knapp FF Jr: Effects of configuration on the myocardial uptake of radioiodinated 3(R)-BMIPP and 3(S)-BMIPP in rats. J Nucl Med 38: 1434–1441, 1997

    Google Scholar 

  13. McDermott JC, Bonen A: Lactate transport by skeletal muscle sarcolemmal vesicles. Mol Cell Biochem 122: 113–121, 1993

    Google Scholar 

  14. McCullagh KJA, Juel C, O'Brien M, Bonen A: Chronic muscle stimulation increases lactate transport in rat skeletal muscle. Mol Cell Biochem 156: 51–57, 1996

    Google Scholar 

  15. Juel C: Muscle lactate transport studied in sarcolemmal giant vesicles. Biochim Biophys Acta 1065: 15–20, 1991

    Google Scholar 

  16. Kristiansen S, Wojtaszewski JF, Juel C, Richter EA: Effect of glucose-6-phosphate and pH on glucose transport in skeletal muscle plasma membrane giant vesicles. Acta Physiol Scand 150: 227–233, 1994

    Google Scholar 

  17. Kristiansen S, Hargreaves M, Richter EA: Progressive increase in glucose transport and GLUT-4 in human sarcolemmal vesicles during moderate exercise. Am J Physiol 272: E385–E389, 1997

    Google Scholar 

  18. Juel C: Lactate - proton cotransport in skeletal muscle. Physiol Rev 77: 1–37, 1997

    Google Scholar 

  19. Bonen A, Luiken JJFP, Lui S, Dyck DJ, Kiens B, Kristiansen S, Turcotte L, van der Vusse GJ, Glatz JFC: Palmitate transport and fatty acid transporters in red and white muscles. Am J Physiol Endocrinol Metab 275: E471–E478, 1998

    Google Scholar 

  20. Luiken JJFP, Arumugam Y, Dyck DJ, Bell RC, Pelsers ML, Turcotte LP, Tandon NN, Glatz JFC, Bonen A: Increased rates of fatty acid uptake and plasmalemmal fatty acid transporters in obese Zucker rats. J Biol Chem 2001 (in press)

  21. Luiken JJFP, Turcotte LP, Bonen A: Protein-mediated palmitate uptake and expression of fatty acid transport proteins in heart giant vesicles. J Lipid Res 40: 1007–1016, 1999

    Google Scholar 

  22. Isola LM, Zhou SL, Kiang CL, Stump DD, Bradbury MW, Berk PD: 3T3 fibroblasts transfected with a cDNA for mitochondrial aspartate aminotransferase express plasma menbrane fatty acid-binding protein and saturable fatty acid uptake. Proc Natl Acad Sci USA 92: 9866-9870, 1995

    Google Scholar 

  23. Hirsch D, Stahl A, Lodish HF: A family of fatty acid transporters conserved from mycobacterium to man. Proc Natl Acad Sci USA 95: 8625–8629, 1998

    Google Scholar 

  24. Schaffer JE, Lodish HF: Molecular mechanism of long-chain fatty acid uptake. Trends Cardiovasc Med 5: 218–224, 1995

    Google Scholar 

  25. Abumrad NA, El-Maghrabi MR, Amri E-Z, Lopez E, Grimaldi P: Cloning of a rat adipocyte membrane protein implicated in binding or transport of long chain fatty acids that is induced during preadipocyte differentiation. Homology with human CD36. J Biol Chem 268: 17665–17668, 1993

    Google Scholar 

  26. Ibrahimi A, Sfeir Z, Magharaine H, Amri EZ, Grimaldi P, Abumrad NA: Expression of the CD36 homolog (FAT) in fibroblast cells: Effects on fatty acid transport. Proc Natl Acad Sci USA 93: 2646–2651, 1996

    Google Scholar 

  27. Memon RA, Fuller J, Moser AH, Smith PJ, Grunfeld C, Feingold KR: Regulation of putative fatty acid transporters and Acyl-CoA synthetase in liver and adipose tissue in ob/ob mice. Diabetes 48: 121–127, 1999

    Google Scholar 

  28. Berk PD, Zhou S-L, Kiang C-L, Stump D, Fan X, Bradbury M: Selective upregulation of fatty acid uptake by adipocytes characterizes both genetic and diet-induced obesity in rodents. J Biol Chem 274: 28626–28631, 1999

    Google Scholar 

  29. Coe R, Johnston-Smith A, Frohnert BI, Watkins PA, Bernlohr DA: The fatty acid transport protein (FATP1) is a very long chain acyl-CoA synthetase. J Biol Chem 274: 36300–36304, 1999

    Google Scholar 

  30. Watkins PA, Lu JF, Steinberg SJ, Gould SJ, Smith KD, Braiterman LT: Disruption of the Saccharomyces cerevisiae FAT1 gene decreases very long-chain fatty acyl-CoA synthetase activity and elevates intracellular very long-chain fatty acid concentrations. J Biol Chem 273: 18210–18219, 1998

    Google Scholar 

  31. Glatz JFC, van Nieuwenhoven FA, Luiken JJFP, Schaap FG, van der Vusse GJ: Role of membrane-associated and cytoplasmic fatty acid binding proteins and cellular fatty acid metabolism. Prostagland Leuk Essent Fatty Acids 4-5: 373–378, 1997

    Google Scholar 

  32. Glatz JFC, Storch J: Unravelling the significance of cellular fatty acid binding proteins. Curr Opin Lipidol 12: 276–274, 2001

    Google Scholar 

  33. Turcotte LP, Swenberger JR, Tucker MZ, Trump G, Yee AJ, Luiken JJFP, Bonen A: Muscle palmitate transport and binding are saturable and inhibited by antibodies to FABPpm. Mol Cell Biochem 210: 53–63, 2000

    Google Scholar 

  34. Van der Vusse GJ, Roemen THM: Gradient of fatty acids from blood plasma to skeletal muscle in dogs. J Appl Physiol 78: 1839–1843, 1995

    Google Scholar 

  35. Bonen A, Dyck DJ, Ibrahimi A, Abumrad NA: Muscle contractile activity increases fatty acid metabolism and transport and FAT/CD36. Am J Physiol (Endocrinol Metab) 276: E642–E649, 1999

    Google Scholar 

  36. Ibrahimi A, Bonen A, Blinn WD, Hajri T, Li X, Zhong K, Cameron R, Abumrad NA: Muscle-specific overexpression of FAT/CD36 enhances fatty acid oxidation by contracting muscles, reduces plasma triglycerides and fatty acids, and increases plasma glucose and insulin. J Biol Chem 274: 26761–26766, 1999

    Google Scholar 

  37. Febbraio M, Abumrad NA, Hajjar DP, Sharma K, Cheng W, Frieda S, Pearce A, Silverstein RL: A null mutation in murine CD36 reveals an important role in fatty acid and lipoprotein metabolism. J Biol Chem 274: 19055–19062, 1999

    Google Scholar 

  38. Dyck DJ, Bonen A: Muscle contraction increases palmitate esterification and oxidation, and triacylglycerol oxidation. Am J Physiol (Endocrinol Metab) 275: E888–E896, 1998

    Google Scholar 

  39. Turcotte LP, Richter EA, Kiens B: Increased plasma FFA uptake and oxidation during prolonged exercise in trained vs. untrained humans. Am J Physiol 262: E791–E799, 1992

    Google Scholar 

  40. Dyck DJ, Steinberg G, Bonen A: Insulin increases FFA uptake and esterification but reduces lipid utilization in isolated contracting muscles. Am J Physiol Endocrinol Metab 281: E600–E607, 2001

    Google Scholar 

  41. Muoio DM, Dohm GL, Tapscott EB, Coleman RA: Leptin opposes insulin's effects on fatty acid partitioning in muscles isolated from obese ob/ob mice. Am J Physiol (Endocrinol Metab) 276: E913–E921, 1999

    Google Scholar 

  42. Bonen A, Luiken JJFP, Arumugam Y, Glatz JFC, Tandon NN: Acute regulation of fatty acid uptake involves the cellular redistribution of fatty acid translocase. J Biol Chem 275: 14501–14508, 2000

    Google Scholar 

  43. Luiken JJFP, Dyck DJ, Han X-X, Tandon NN, Arumugam Y, Glatz JFC, Bonen A: Insulin induces the translocation of the fatty acid transporter FAT/CD36 to the plasma membrane. Am J Physiol Endocrinol Metab 2001 (in press)

  44. Lemieux K, Han X-X, Dombrowski L, Bonen A, Marette A: The transferrin receptor defines two distinct contraction-responsive GLUT4 vesicle populations. Diabetes 49: 183–189, 2000

    Google Scholar 

  45. Pan DA, Lillioja S, Kriketos AD, Milner MR, Baur LA, Jenkins AB, Storlien LH: Skeletal muscle triglyceride levels are inversely related to insulin action. Diabetes 46: 983–988, 1997

    Google Scholar 

  46. Brozinick JT Jr, Etgen GJ, Yaspelkis BB III, Kang HY, Ivy JL: Effects of exercise training on muscle GLUT-4 protein content and translocation in obese Zucker rats. Am J Physiol (Endocrinol Metab) 265: E419–E427, 1993

    Google Scholar 

  47. Uphues I, Kolter T, Goud B, Eckel J: Failure of insulin-regulated recruitment of the glucose transporter GLUT4 in cardiac muscle of obese Zucker rats is associated with alterations of small-molecular-mass GTPbinding proteins. Biochem J 311: 161–166, 1995

    Google Scholar 

  48. Pelsers ML, Lutgerink JT, van Nieuwenhoven FA, Tandon NN, van der Vusse GJ, Arends JW, Hoogenboom HR, Glatz JFC: A sensitive immunoassay for rat fatty acid translocase (CD36) using phage antibodies selected on cell transfectants: Abundant presence of fatty acid translocase/CD36 in cardiac and red skeletal muscle and up-regulation in diabetes. Biochem J 337: 407–414, 1999

    Google Scholar 

  49. Yaskelpis III BB, Ansari L, Ramey EA, Loy SF: Chronic leptin administration increases insulin-stimulated skeletal muscle glucose uptake. Metabolism 48: 671–676, 1999

    Google Scholar 

  50. Steinberg GR, Dyck DJ, Calles-Escandon J, Tandon NN, Luiken JJFP, Glatz JF, Bonen A: Chronic leptin administration decreases fatty acid uptake and fatty acid transporters in rat skeletal muscle. J Biol Chem 2002 (in press)

  51. Kelley DA, Mandarino LJ: Fuel selection in human skeletal muscle in insulin resistance. A reexamination. Diabetes 49: 677–683, 2000

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bonen, A., Luiken, J.J. & Glatz, J.F. Regulation of fatty acid transport and membrane transporters in health and disease. Mol Cell Biochem 239, 181–192 (2002). https://doi.org/10.1023/A:1020511125085

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1020511125085

Navigation