Skip to main content

Effect of Ischemia—Reperfusion on Na+,K+-ATPase Expression in Human Liver Tissue Allograft: Image Analysis by Confocal Laser Scanning Microscopy

  • Published:
Digestive Diseases and Sciences Aims and scope Submit manuscript

Abstract

We have analyzed the effect of Ischemia—Reperfusion on expression of hepatic Na+,K+-ATPase on bile canalicular (BCM) and basolateral membranes (BLM) in human liver allografts using confocal laser scanning microscopy imaging. Na+,K+-ATPase, an integral membrane enzyme, plays a key role in the physiology and structure of hepatocytes, where it maintains the electrochemical gradients for Na+ and K+ across the cell membrane. The concentrations of these ions as well as their gradients regulate the active transport across the plasma membrane for bile acid and water from sinusoidal to canalicular membranes. In addition, Na+,K+-ATPase is also involved in cellular structure because of its close relationship with submembrane microfilaments and its implication in tight junction assembly. Therefore, Na+,K+-ATPase appears as an indicator of tissue viability and hepatic functionality during liver transplantation. Its localization and its function in BCM are still controversial. As in previous studies, we found an enzyme expression in both BLM and BCM. We show that ischemia induced a decrease in Na+,K+-ATPase expression only in BCM. This result could be explained by the differences in biochemical membrane environment between basolateral and bile canalicular Na+,K+-ATPase. Membrane lipid fluidity, which is more elevated in BLM than in BCM, could protect the enzyme during ischemia. After reperfusion, Na+,K+-ATPase expression was strongly decreased in both BCM and BLM. This alteration following reperfusion is probably due to multiple factors: direct alteration of the enzyme catalytic subunit and modification of its environment and membrane lipid fluidity by free radicals and changes in ATP levels and ionic distribution. This important decrease in Na+,K+-ATPase expression of both BLM and BCM could disturb not only hepatic secretory function but also cellular volume and structure during the postoperative period.

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

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price includes VAT (Canada)

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  1. Bremer C, Bradford BU, Hunt KJ, Knecht KT, Connor HD, Mason RP, Thurman RG: Role of Kupffer cells in the pathogenesis of hepatic reperfusion injury. Am J Physiol 267:G30–G36, 1994

    Google Scholar 

  2. Jaeschke H, Bautista AP, Spolarics Z, Spitzer JJ: Superoxide generation by Kupffer cells and priming of neutrophils during reperfusion after hepatic ischemia. Free Radic Res Commun 15:277–284, 1991

    Google Scholar 

  3. Jaeschke H, Smith CW, Clemens MG, Ganey PE, Roth RA: Contemporary issues in toxicology. Mechanisms of inflammatory liver injury: Adhesion molecules and cytotoxicity of neutrophils. Toxicol Appl Pharmacol 139:213–226, 1996

    Google Scholar 

  4. Benkoël L, Dodero F, Hardwigsen J, Benoliel AM, Bongrand P, Botta-Fridlund D, Le Treut YP, Chamlian A, Lombardo D: Expression of intercellular adhesion molecule-1 (ICAM-1) during ischemia-reperfusion in human liver tissue allograft: Image analysis by confocal laser scanning microscopy. Dig Dis Sci 48:2167–2172, 2003

    Google Scholar 

  5. Toledo-Pereyra LH, Suzuki S: Neutophils, cytokines and adhesion molecules in hepatic ischemia and reperfusion injury. J Am Coll Surg 179:758–762, 1994

    Google Scholar 

  6. Muriel P, Sandoval G: Nitric oxide and peroxynitrite anion modulate liver plasma membrane fluidity and Na+/K+-ATPase activity. Nitic Oxide 4:333–342, 2000

    Google Scholar 

  7. Lee SM, Park MJ, Cho TS, Clemens MG: Hepatic injury and lipid peroxidation during ischemia and reperfusion. Shock 13:279–284, 2000

    Google Scholar 

  8. Kourie JI: Interaction of reactive oxygen species with ion transport mechanisms. Am J Physiol 275:C1–C24, 1998

    Google Scholar 

  9. Song JY, Van Marle J, Van Noorden CJF, Frederiks WF: Redistribution of Ca2+, Mg2+-ATPase activity in relation to alterations of the cytoskeleton and tight junctions in hepatocytes of cholestatic rat liver. Eur J Cell Biol 71:277–285, 1996

    Google Scholar 

  10. Morrow JS, Cianci CD, Ardito T, Mann AS, Kashgarian M: Ankyrin links fodrin to the alpha subunit of the Na+, K+-ATPase in Madin-Darby canine kidney cells and in intact renal tubule cells. J Cell Biol 108:445–465, 1989

    Google Scholar 

  11. Nelson WJ, Veshnock PJ: Ankyrin binding to (Na+ + K+)ATPase and implications for the organization of membrane domains in polarized cells. Nature 328:533–536, 1987

    Google Scholar 

  12. Rajasekaran AK, Rajasekaran SA: Role of Na-K-ATPase in the assembly of tight junctions. Am J Physiol 285:F388–F396, 2003

    Google Scholar 

  13. Blitzer BL, Boyer JL: Localization of Na+ K+-ATPase on the hepatocyte plasma membrane. Gastroenterology 87:1206–1207, 1984

    Google Scholar 

  14. Boyer JL, Allen RM, Cheng Ng O: Biochemical separation of Na+ K+-ATPase from a “purified” light density, “canalicular”-enriched plasma membrane fraction from rat liver. Hepatology 3:18–28, 1983

    Google Scholar 

  15. Gorvel JP, Liaboeuf A, Massey D, Liot D, Goridis C, Maroux S: Recognition of sodium-and potassium-dependent adenosine triphos-phatase in organs of the mouse by means of monoclonal antibody. Cell Tissue Res 234:619–632, 1983

    Google Scholar 

  16. Meier PJ, Sztul ES, Reuben A, Boyer JL: Structural and functional polarity of canalicular and basolateral plasma membrane vesicles isolated in high yield from rat liver. J Cell Biol 98:991–1000, 1984

    Google Scholar 

  17. Sztul ES, Biemesderfer D, Caplan MJ, Kashgarian M, Boyer JL: Localization of Na+ K+-ATPase α-subunit to the sinusoidal and lateral but not canalicular membranes of rat hepatocytes. J Cell Biol 104:1239–1248, 1987

    Google Scholar 

  18. Yamamoto K, Mayahara H, Ogawa K: Cytochemical localization of ouabain-sensitive, K-dependent p-nitrophenylphosphate in the rat hepatocyte. Acta Histochem Cytochem 17:23–35, 1984

    Google Scholar 

  19. Hara T, Kudou M, Otake K, Hayashi T, Asano G: Immunohisto-chemical localization of Na+ K+-ATPase in human liver. Acta Histochem Cytochem 21:593–599, 1988

    Google Scholar 

  20. Leffert HL, Schenk DB, Hubert JJ, Skelly H, Schumacher M, Ariyasu R, Ellisman M, Koch KS, Keller GA: Hepatic (Na+ K+ )-ATPase: A current view of its structure, function and localization in rat liver as revealed by studies with monoclonal antibodies. Hepatology 5:501–507, 1985

    Google Scholar 

  21. Schenk DB, Leffert HL: Monoclonal antibodies to rat Na+ K+-ATPase block enzymatic activity. Proc Natn Acad Sci 80:5281–5285, 1983

    Google Scholar 

  22. Sutherland E, Dixon BS, Leffert HL, Skally H, Zaccaro L, Simon FR: Biochemical localization of hepatic surface-membrane Na+ K+-ATPase activity depends on membrane lipid fluidity. Proc Natl Acad Sci USA 85:8673–8677, 1988

    Google Scholar 

  23. Takemura S, Omori K, Tanaka K, Omori K, Matsuura S, Tashiro Y: Quantitative immunoferritin localization of (Na+ K+)-ATPase on canine hepatocyte cell surface. J Cell Biol 99:1502–1510, 1984

    Google Scholar 

  24. Chamlian A, Benkoël L, Chrestian MA, Di Costanzo-Dufetel J, Cano N, Di Costanzo J: Cytochemical localization of ouabain sensitive, K++dependent p-nitrophenyl phosphatase in human liver. Its relationship to Na+ K+-ATP-A. Cell Mol Biol 34:215–222, 1988

    Google Scholar 

  25. Benkoël L, Benoliel AM, Brisse J, Sastre B, Bongrand P, Chamlian A: Immunocytochemical study of Na+ K+-ATPase α1 and β1 subunits in human and rat normal hepatocytes using confocal microscopy. Cell Mol Biol 41:499–504, 1995

    Google Scholar 

  26. Benkoël L, Chanussot F, Dodero F, De la Maisonneuve C, Lambert R, Brisse J, Chamlian A: Effect of dietary lipids on hepatic Na+, K+-ATPase in cyclosporine A-treated rats. Immunocytochemical analysis of α subunit by confocal laser scanning microscopy imaging. Dig Dis Sci 44:1643–1649, 1999

    Google Scholar 

  27. Sennoune S, Gerbi A, Duran MJ, Benkoël L, Pierre S, Lambert R, Dodero F, Chamlian A, Vague P, Maixent JM: A quantitative immunocytochemical study of Na+ K+-ATPase in rat hepatocytes after STZ-induced diabetes and dietary fish oil supplementation. J Histochem Cytochem 47:809–816, 1999

    Google Scholar 

  28. Sellinger M, Barrett C, Malle P, Gordon ER, Boyer JL: Cryptic Na+ K+-ATPase activity in rat liver canalicular plasma membranes: evidence for its basolateral origin. Hepatology 11:223–229, 1990

    Google Scholar 

  29. Paller MS: Lateral mobility of Na, K-ATPase and membrane lipids in renal cells. Importance of cytoskeletal integrity. J Membr Biol 142:127–135, 1994

    Google Scholar 

  30. Molitoris BA: Na(+)-K(+)-ATPase that redistributes to apical membrane during ATP depletion remains functional. Am J Physiol 265:F693–F697, 1993

    Google Scholar 

  31. Lemas MV, Hamrick M, Takeyasu K, Fambrough DM: 26 Amino acids of an extracellular domain of the Na+K-ATPase α-subunit are sufficient for assembly with the the Na+K-ATPase β-subunit. J Biol Chem 269:8255–8259, 1994

    Google Scholar 

  32. Lingrel JB, Orlowski J, Shull MM, Price EM: Molecular genetics of Na K-ATPase. Prog Nucl Acid Res Mol Biol 38:37–89, 1990

    Google Scholar 

  33. Chanussot F, Benkoël L: Prevention by dietary (n-6) polyunsatu-rated phosphatidylcholines of intrahepatic cholestasis induced by cyclosporine A in animals. Life Sci 73:381–392, 2003

    Google Scholar 

  34. Mizoe A, Kondo S, Azuma T, Fujioka H, Tanaka K, Hashida M, Kanematsu T: Preventive effects of superoxide dismutase derivatives modified with monosaccharides on reperfusion injury in rat liver transplantation. J Surg Res 73:160–165, 1997

    Google Scholar 

  35. Angermüller S, Schunk M, Kusterer K, Konrad T, Usadel KH: Alterations of Na+, K+-ATPase activity after hypoxia and reoxygenation in the perfused rat liver: an electron microscopic cytochemical study. J Hepatol 22:565–575, 1995

    Google Scholar 

  36. Coux G, Trumper L, Elias MM: renal function and cortical (Na+ + K+)-ATPase activity, abundance and distribution after ischaemia-reperfusion in rats. Biochim Biophys Acta 1586:71–80, 2002

    Google Scholar 

  37. André P, Benoliel AM, Capo C, Foa C, Buferne M, Boyer C, Schmitt-Verhults AM, Bongrand P: Use of conjugates made between a cytolytic T cell clone and target cells to study the distribution of membrane molecules in cell contact areas. J Cell Sci 97:335–347, 1990

    Google Scholar 

  38. Benkoël L, Dodero F, Hardwigsen J, Campan P, Botta-Fridlund D, Lombardo D, Le Treut YP, Chamlian A: Effect of ischemia-reperfusion on bile canalicular F-actin microfilaments in hepatocytes of human liver allograft. Image analysis by confocal laser scanning microscopy. Dig Dis Sci 46:1663–1667, 2001

    Google Scholar 

  39. Farber JL, Chien KR, Mittnacht S: The pathogenesis of irreversible cell injury in ischemia. Am J Pathol 102:271–280, 1981

    Google Scholar 

  40. Florine-Casteel K, Lemasters JJ, Herman B: Digitized fluorescence polarization microscopy of DPH and related probes in cell-size vesicles composed of gel or fluid-phase phospholipid. In Optical Microscopy for Biology. K Jacobson, B Herman (eds). New York, Wiley-Liss, 1990, pp 559–573

    Google Scholar 

  41. Carini R, De Cesaris MG, Bellomo G, Albano E: Intracellular Na+ accumulation and hepatocyte injury during cold storage. Transplantation 68:294–297, 1999

    Google Scholar 

  42. Carini R, De Cesaris MG, Splendore R, Bagnati M, Bellomo G, Albano E: Alterations of Na+ homeostasis in hepatocyte reoxy-genation injury. Biochim Biophys Acta 1500:297–305, 2000

    Google Scholar 

  43. Arora AS, De Groen P, Emori Y, Gores GJ: Acascade of degradative hydrolase activity contributes to hepatocyte necrosis during anoxia. Am J Physiol 270:G238–G245, 1996

    Google Scholar 

  44. Dang AQ, Kemp K, Faas FH, Carter WJ: Effects of dietary fats on fatty acid composition and delta 5 desaturase in normal and diabetic rats. Lipids 24:882–889, 1989

    Google Scholar 

  45. Ng YC, Tolerico PH, Book CBS: Alterations in levels of Na+ K+-ATPase isoforms in heart, skeletal muscle and kidney of diabetic rats. Am J Physiol 265:E243–E251, 1993

    Google Scholar 

  46. Angermüller S, Steinmetz I, Weber T, Czerny F, Hanisch E, Kusterer K: Significant increase of Kupffer cells associated with loss of Na+, K+-ATPase activity in rat hepatic allograft rejection. Transplantation 63:1562–1570, 1997

    Google Scholar 

  47. Ingbar DH, Wendt CH: The sodium pump and oxidant stress: If only it were so simple. J Lab Clin Med 130:119–122, 1997

    Google Scholar 

  48. Mense M, Stark G, Apell HJ: Effects of free radicals on partial reaction of the Na, K-ATPase. J Membr Biol 156:63–71, 1997

    Google Scholar 

  49. Lehotsky J, Kaplan P, Matejovicova M, Murin R, Racay P, Raeymaekers L: Ion transport systems as targets of free radicals during ischemia reperfusion injury. Gen Physiol Biophys 21:31–37, 2002

    Google Scholar 

  50. Huang WH, Wang Y, Askari A: (Na+ + K+)-ATPase: Inactivation and degradation induced by oxygen radicals. Int J Biochem 24:621–626, 1992

    Google Scholar 

  51. Kako K, Kato M, Matsuoka T, Mustapha A: Depression of membrane-bound Na+-K+ATPase activity induced by free radicals and by ischemia of kidney. Am J Physiol 254:C330–C337, 1988

    Google Scholar 

  52. Muriel P, Castaneda G, Ortega M, Noël F: Insights into the mechanism of erythrocyte Na+/K+-ATPase inhibition by nitric oxide and peroxynitrite anion. J Appl Toxicol 23:275–278, 2003

    Google Scholar 

  53. Green RM, Whiting JF, Rosenbluth AB, Beier D, Gollan JL: Interleukin-6 inhibits hepatocyte taurocholate uptake and sodium-potassium-adenosinetriphosphatase activity. Am J Physiol 267: G1094–G1100, 1994

    Google Scholar 

  54. Carini R, De Cesaris MG, Splendore R, Domenicotti C, Nitti MP, Pronzato MA, Albano E: Mechanisms of hepatocyte protection against hypoxic injury by atrial natriuretic peptide. Hepatology 37:277–285, 2003

    Google Scholar 

  55. Quintana AB, Rodriguez JV, Scandizzi AL, Guibert EE: The benefit of adding sodium nitroprusside (NPNa) or S-nitrosoglutathion (GSNO) to the University of Wisconsin solution (UW) to prevent morphological alterations during cold preservation/reperfusion of rat livers. Ann Hepatol 2:84–91, 2003

    Google Scholar 

  56. Schauer RJ, Kalmuk S, Gerbes AL, Leiderer R, Meissner H, Schildberg FW, Messmer K, Bilzer M: Intravenous administration of glutathione protects parenchymal and non-parenchymal liver cells against reperfusion injury following rat liver transplantation. World J Gastroenterol 10:864–870, 2004

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Benkoel, L., Dodero, F., Hardwigsen, J. et al. Effect of Ischemia—Reperfusion on Na+,K+-ATPase Expression in Human Liver Tissue Allograft: Image Analysis by Confocal Laser Scanning Microscopy. Dig Dis Sci 49, 1387–1393 (2004). https://doi.org/10.1023/B:DDAS.0000042235.72622.16

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/B:DDAS.0000042235.72622.16