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Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vitro

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In this chapter we describe in details the permeabilized cell and skinned fiber techniques and their applications for studies of mitochondrial function in vivo. The experience of more than 10 years of research in four countries is summarized. The use of saponin in very low concentration (50-100 μg/ml) for permeabilisation of the sarcolemma leaves all intracellular structures, including mitochondria, completely intact. The intactness of mitochondrial function in these skinned muscle fibers is demonstrated in this work by multiple methods, such as NADH and flavoprotein fluorescence studies, fluorescence imaging, confocal immunofluorescence microscopy and respiratory analysis. Permeabilized cell and skinned fiber techniques have several very significant advantages for studies of mitochondrial function, in comparison with the traditional methods of use of isolated mitochondria: (1) very small tissue samples are required; (2) all cellular population of mitochondria can be investigated; (3) most important, however, is that mitochondria are studied in their natural surrounding. The results of research by using this method show the existence of several new phenomenon - tissue dependence of the mechanism of regulation of mitochondrial respiration, and activation of respiration by selective proteolysis. These phenomena are explained by interaction of mitochondria with other cellular structures in vivo. The details of experimental studies with use of these techniques and problems of kinetic analysis of the results are discussed. Examples of large-scale clinical application of these methods are given.

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References

  1. Veksler VI, Kuznetsov AV, Sharov VG, Kapelko VI, Saks VA: mitochondrial respiratory parameters in cardiac tissue: A novel method of assessment by using saponin-skinned fibers. Biochim Biophys Acta 892: 191–196, 1987

    Google Scholar 

  2. Endo M, Kitazawa T: E-C coupling studies in skinned cardiac fibers. In: M Morad (ed). Biophysical Aspects of Cardiac Muscle, Academic, New York, 1978 pp 307–327

    Google Scholar 

  3. Glauert A, Dingle J, Lucy J: Action of saponin on biological cell membranes. Nature 196: 952–955, 1962

    Google Scholar 

  4. Korn E: Cell membranes: Structure and synthesis. Annul Rev Biochem 38: 263–288, 1969

    Google Scholar 

  5. Comte J, Maisterrena B, Gautheron DC: Lipid composition and protein profiles of outer and inner membranes from pig heart mitochondria comparison with microsomes. Biochim Biophys Acta 419: 271–284, 1976

    Google Scholar 

  6. Saks VA, Kuznetsov AV, Kupriyanov VV, Micely MV, Jacobus WE: Creatine kinase of rat heart mitochondria. The demonstration of functional coupling to oxidative phosphorylation in an inner membrane-matrix preparation. J Biol Chem 260: 7757–7764, 1985

    Google Scholar 

  7. Bygrave FL, Lehninger AL: The affinity of mitochondrial oxidative phosphorylation mechanism for phosphate and adenosine diphosphate. Proc Natl Acad Sci USA 57: 1409–1414, 1967

    Google Scholar 

  8. Wiseman RW, Jeneson JAL, Kushmerick MJ: Why is the sensitivity of mitochondria to ADP over tenfold lower in permeabilized fibers than in vivo? Biothermokinetics ofthe living cell. Biothermokinetics Press, Amsterdam, 1996 pp 124–127

    Google Scholar 

  9. Altschuld RA, Wenger WC, Lamka KG, Kindig OR, Capen CC, Mizuhira V, Vander Heide RS, Brierley GP: Structural and functional properties of adult rat heart myocytes lysed with digitonin. J Biol Chem 260: 14325–14334, 1985.

    Google Scholar 

  10. Saks VA, Vasil'eva E, Belikova YO, Kuzuetsov AV, Lyapina S, Petrova L, Perov NA: Retarded diffusion of ADP in cardiomyocytes: Possible role of mitochondrial outer membrane and creatine kinase in cellular regulation of oxidative phosphorylation. Biochim Biophys Acta 1144: 134–148, 1993

    Google Scholar 

  11. Saks VA, Behkova YO, Kuznetsov AV: In vivo regulation of mitochondrial respiration in cardiomyocytes: Specific restriction for intracellular diffusion of ADP. Biochim Biophys Acta 1074: 302–311, 1991

    Google Scholar 

  12. Penman S: Rethinking cell structure. Proc Natl Acad Sci USA 92: 5251–5257, 1995

    Google Scholar 

  13. Lin A, Krockmalnic G, Penman S: imaging cytoskeleton-mitochondrial membrane attachments by embedment-free electron-microscopy of saponin-extracted cells. Proc Natl Acad Sci USA 87: 8565–8569, 1990

    Google Scholar 

  14. Kunz WS, Kuzuetsov AV, Schulze W, Eichhorn K, Schild L, Striggow F, Bohnensack R, Neuhof S, Grasshoff H, Neumann HW, Gellerich FN: Functional characterization of mit ochondrial oxidative phosphorylation in saponinskinned human muscle fibers. Biochim Biophys Acta 1144: 46–53, 1993

    Google Scholar 

  15. Vignais PV: Molecular and physiological aspects of adenine nucleotide transport in mitochondria. Biochim Biophys Acta 456: 1–38, 1976

    Google Scholar 

  16. Minayeva A, Ventura-Clapier R, Veksler V: Ca2+ uptake by sarcoplasmic reticulum ATPase in situ strongly depends on bound creatine kinase. Pflugers Arch-Eur J Physiol 432: 904–912, 1996

    Google Scholar 

  17. Livingston BE, Altschuld RA, Hohl CM: Metabolic compartmentalization in neonatal swine myocytes. Pediatric Research 40: 59–65, 1990

    Google Scholar 

  18. Kunz WS, Kuzuetsov AV, Gellerich FN: Mitochondrial oxidative phopshorylation in saponin-skinned human muscle fibers is stimulated by caffeine. FEBS Lett 323: 188–190, 1993

    Google Scholar 

  19. Ouhabi R, Boue-Grabot M, Mazat J-P: ATP synthesis in permeabilized cells: assessment ofthe ATP/O ratio in situ. In: E. Gnaiger, F.N. Gellerich, M. Wyss (eds). Modern Trends in Biothermokinetics, Innsbruck University Press, vol. 3 1994 pp 141–144

  20. Vercesi AE, Bernardes CF, Hoffmann ME, Gadelha FR, Docampo R: Digitonin permeabilization deos not affect mitochondrial function and allows the determination of the mitochondrial membrane potential of Trypanosoma cruzi in situ. J Biol Chem 266: 14431–14434, 1991

    Google Scholar 

  21. Saks VA, Kapelko VI, Kupriyanov VV, Kuznetsov AV, Lakomkin VL, Veksler VI, Sharov VG, Javadov SA, Seppet EK: Quantitative evaluation of relationship between cardiac energy metabolism and postischemic recovery of contractile function. J Mol Cell Cardiol 21: (Suppl) 67–78, 1989

    Google Scholar 

  22. Veksler V, Ventura-Clapier R: In situ study of myofibrils, mitochondria and bound creatine kineses in experimental cardiomyopathies. Mol Cell Biochem 133/134: 287–298, 1994

    Google Scholar 

  23. Saks VA, Khuchua ZA, Vasilyeva EV, Belikova YO, Kuzuetsov AV: Metabolic compartmentation and substrate channelling in muscle cells. Role of coupled creatine kineses in in vivo regulation of cellular respiration-a synthesis. In: V. Saks, R. Ventura-Clapier (eds) Cellular bioenergetics: Role of coupled creatine kineses, Kluwer Academic Publishers, Dordrecht-Boston-London, 1994 pp 155–192

    Google Scholar 

  24. Saks VA, Kuznetsov AV, Khuchua ZA, Vasilieva EV, Belikova YO, Kesvatera T, Tiivel T: Control of cellular respiration in vivo by mitochondrial outer membrane and by creatine kinase. A new speculative hypothesis: Possible involvement of mitochondrial cytoskeletal interactions. J Mol Cell Cardiol 27: 625–645, 1995

    Google Scholar 

  25. Saks VA, Belikova YO, Vasileva EV, Kuzuetsov AV, Fontain E, Keriel C, Leverve X: Correlation between degree of rupture of outer mitochondrial membrane and change of kinetics of regulation of respiration by ADP in permeabilized heart and liver cells. Biochem Biophys Res Comm 208: 919–926, 1995

    Google Scholar 

  26. Veksler VI, Kuznetsov AV, Anflous K, Mateo P, van Deursen J, Be Wieringa, Ventura-Clapier Z: Muscle creatine kinase deficient mice. II Cardiac and skeletal muscles exhibit tissue-specific adaptation of the mitochondrial function. J Biol Chem 270: 19921–19929, 1995

    Google Scholar 

  27. Saks VA, Ventura-Clapier R, Aliev MK: Metabolic control and 37 metabolic capacity: Two aspects of creatine kinase functioning in the cells. Biochim Biophys Acta 1274: 81–88, 1996

    Google Scholar 

  28. Kakol I, Borovikov YS, Szczesna D, Kirillova VP, Levitsky DI: Conformational changes of F-actin in myosin-free ghost single fibre induced by either phosphorylated or dephosphorylated heavy meromyosin. Biochin1 Biophys Acta 913: 1–9, 1987

    Google Scholar 

  29. Kunz WS, Kuznetsov AV, Winkler K, Gellerich FN, Nenhof S, Neumann HW: Measurement of fluorescence changes of NADH and of fluorescent flavoproteins in saponin-skinned human skeletal muscle fibers. Anal Biochem 216: 322–327, 1994

    Google Scholar 

  30. Winkler K, Kuznetsov AV, Lins H, Kirches E, Von Bossany P, Dietzmann K, Frank B, Feistner H, Kunz WS: Laser-excited fluorescence studies of mitochondrial function in saponin-skinned skeletal muscle fibers of patients with chronic progressive external ophthalmoplegia. Biochim Biophys Acta 1272: 181–184, 1995

    Google Scholar 

  31. Kunz WS, Gellerich FN: Quantification of the content of fluorescent flavoprateins in mitochondria from rat liver, kidney cortex, skeletal muscle and brain. Biochim Med Metab Biol 50: 103–110, 1993

    Google Scholar 

  32. Granger BL, Lazarides E: Desmin and vimentin coexist at the perifery of myofibril Z-disc. Cell 18: 1053–1066, 1979

    Google Scholar 

  33. Quistorff B, Haselgrove JC, Chance B: High spatial resolution readout of 3D metabolic organ structure: an automated, low-temperature redoxratio scanning instrument. Anal Biochem 148: 389–400, 1985

    Google Scholar 

  34. Kuznetsov AV, Sikk P, Kaambre P, Kay L, Daneshrad Z, Rossi A, Kadaja L, Peet N, Seppet E, Saks VA: Stricking differences between the kinetics of regulation of respiration by ADP in slow-twitch and fast-twitch muscles in vivo. Eur J Biochem 241: 909–915, 1996

    Google Scholar 

  35. Khuchua ZA, Vasileva EV, Clark JF, Korchazhkina OV, Branishte T, Kapelko VI, Kuznetsov AV, Ventura-Clapier R, Steinschneider AYa, Lakomkin VL, Runge EK, Saks VA: The creatine kinase system and cardiomyopathy. Am J Cardiovasc Pathol 4: 223–234, 1992

    Google Scholar 

  36. Saks VA, Belikova YO, Kuzuetsov AV, Khuchua ZA, Branishte TH, Semenovsky ML, Naumov VG: Phosphocreatine pathway for energy transport: ADP diffusion and transport. Am J Physiol Suppl 261: 30–38, 1991

    Google Scholar 

  37. Kuzuetsov AV, Winkler K, Kirches E, Lins H, Feishner H, Kunz WS: Application of inhibitor titrations for the detection of oxidative phosphorylation defects in saponin-skinned muscle fibers of patients with mitochondrial diseases. Biochim Biophys Acta 1997 (in press)

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Veksler, V.I., Kuznetsov, A.V., Kay, L. et al. Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vitro. Mol Cell Biochem 184, 81–100 (1998). https://doi.org/10.1023/A:1006834912257

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