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High-Resolution Respirometry: OXPHOS Protocols for Human Cells and Permeabilized Fibers from Small Biopsies of Human Muscle

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Mitochondrial Bioenergetics

Part of the book series: Methods in Molecular Biology ((MIMB,volume 810))

Abstract

Protocols for high-resolution respirometry (HRR) of intact cells, permeabilized cells, and permeabilized muscle fibers offer sensitive diagnostic tests of integrated mitochondrial function using standard cell culture techniques and small needle biopsies of muscle. Multiple substrate–uncoupler–inhibitor titration (SUIT) protocols for analysis of oxidative phosphorylation improve our understanding of mitochondrial respiratory control and the pathophysiology of mitochondrial diseases. Respiratory states are defined in functional terms to account for the network of metabolic interactions in complex SUIT protocols with stepwise modulation of coupling and substrate control. A regulated degree of intrinsic uncoupling is a hallmark of oxidative phosphorylation, whereas pathological and toxicological dyscoupling is evaluated as a mitochondrial defect. The noncoupled state of maximum respiration is experimentally induced by titration of established uncouplers (FCCP, DNP) to collapse the proton gradient across the mitochondrial inner membrane and measure the capacity of the electron transfer system (ETS, open-circuit operation of respiration). Intrinsic uncoupling and dyscoupling are evaluated as the flux control ratio between nonphosphorylating LEAK respiration (electron flow coupled to proton pumping to compensate for proton leaks) and ETS capacity. If OXPHOS capacity (maximally ADP-stimulated oxygen flux) is less than ETS capacity, the phosphorylation system contributes to flux control. Physiological Complex I + II substrate combinations are required to reconstitute TCA cycle function. This supports maximum ETS and OXPHOS capacities, due to the additive effect of multiple electron supply pathways converging at the Q-junction. Substrate control with electron entry separately through Complex I (pyruvate + malate or glutamate + malate) or Complex II (succinate + rotenone) restricts ETS capacity and artificially enhances flux control upstream of the Q-cycle, providing diagnostic information on specific branches of the ETS. Oxygen levels are maintained above air saturation in protocols with permeabilized muscle fibers to avoid experimental oxygen limitation of respiration. Standardized two-point calibration of the polarographic oxygen sensor (static sensor calibration), calibration of the sensor response time (dynamic sensor calibration), and evaluation of instrumental background oxygen flux (systemic flux compensation) provide the unique experimental basis for high accuracy of quantitative results and quality control in HRR.

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Abbreviations

CCP:

Coupling control protocol

E :

Electron transfer system capacity

FCR:

Flux control ratio

HRR:

High-resolution respirometry

L :

LEAK respiration

mt:

Mitochondrial

O2k:

Oxygraph-2k

P :

OXPHOS capacity

POS:

Polarographic oxygen sensor

R :

ROUTINE respiration

ROX:

Residual oxygen consumption

SUIT:

Substrate–uncoupler–inhibitor titration

W w :

Wet weight

References

  1. Gnaiger E, Steinlechner-Maran R, Méndez G, Eberl T, Margreiter R (1995) Control of mitochondrial and cellular respiration by oxygen. J Bioenerg Biomembr 27:583–596

    Article  PubMed  CAS  Google Scholar 

  2. Gnaiger E (2001) Bioenergetics at low oxygen: dependence of respiration and phosphorylation on oxygen and adenosine diphosphate supply. Respir Physiol 128:277–297

    Article  PubMed  CAS  Google Scholar 

  3. Gnaiger E (2008) Polarographic oxygen sensors, the oxygraph and high-resolution respirometry to assess mitochondrial function. In: Dykens JA, Will Y (eds) Mitochondrial dysfunction in drug-induced toxicity. Wiley, New York, pp 327–352

    Google Scholar 

  4. Gnaiger E (2009) Capacity of oxidative phosphorylation in human skeletal muscle. New perspectives of mitochondrial physiology. Int J Biochem Cell Biol 41:1837–1845

    Article  PubMed  CAS  Google Scholar 

  5. Gnaiger E (2003) Oxygen conformance of cellular respiration: a perspective of mitochondrial physiology. Adv Exp Med Biol 543:39–56

    Article  PubMed  CAS  Google Scholar 

  6. Gnaiger E, Kuznetsov AV, Schneeberger S, Seiler R, Brandacher G, Steurer W, Margreiter R (2000) Mitochondria in the cold. In: Heldmaier G, Klingenspor M (eds) Life in the cold. Springer, New York, pp 431–442

    Google Scholar 

  7. Fasching M, Renner-Sattler K, Gnaiger E (2010) Mitochondrial respiration medium – MiR06. Mitochondr Physiol Netw 14(13): 1–4. http://www.oroboros.at

    Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  9. Skladal D, Sperl W, Schranzhofer R, Krismer M, Gnaiger E, Margreiter R, Gellerich FN (1994) Preservation of mitochondrial functions in human skeletal muscle during storage in high energy preservation solution (HEPS). In: Gnaiger E, Gellerich FN, Wyss M (eds) What is controlling life? vol 3, Modern Trends in Biothermokinetics. Innsbruck University Press, Innsbruck, pp 268–271

    Google Scholar 

  10. Gnaiger E, Méndez G, Hand SC (2000) High phosphorylation efficiency and depression of uncoupled respiration in mitochondria under hypoxia. Proc Natl Acad Sci USA 97:11080–11085

    Article  PubMed  CAS  Google Scholar 

  11. Steinlechner-Maran R, Eberl T, Kunc M, Margreiter R, Gnaiger E (1996) Oxygen dependence of respiration in coupled and uncoupled endothelial cells. Am J Physiol 271:C2053–C2061

    PubMed  CAS  Google Scholar 

  12. Renner K, Amberger A, Konwalinka G, Kofler R, Gnaiger E (2003) Changes of mitochondrial respiration, mitochondrial content and cell size after induction of apoptosis in leukemia cells. Biochim Biophys Acta 1642:115–123

    Article  PubMed  CAS  Google Scholar 

  13. Steinlechner-Maran R, Eberl T, Kunc M, Schröcksnadel H, Margreiter R, Gnaiger E (1997) Respiratory defect as an early event in preservation/reoxygenation injury in endothelial cells. Transplantation 63:136–142

    Article  PubMed  CAS  Google Scholar 

  14. Stadlmann S, Rieger G, Amberger A, Kuznetsov AV, Margreiter R, Gnaiger E (2002) H2O2-mediated oxidative stress versus cold ischemia-reperfusion: mitochondrial respiratory defects in cultured human endothelial cells. Transplantation 74:1800–1803

    Article  PubMed  CAS  Google Scholar 

  15. Hütter E, Renner K, Pfister G, Stöckl P, Jansen-Dürr P, Gnaiger E (2004) Senescence-associated changes in respiration and oxidative phosphorylation in primary human fibroblasts. Biochem J 380:919–928

    Article  PubMed  Google Scholar 

  16. Hütter E, Unterluggauer H, Garedew A, Jansen-Dürr P, Gnaiger E (2006) High-resolution respirometry – a modern tool in aging research. Exp Gerontol 41:103–109

    Article  PubMed  Google Scholar 

  17. Aguirre E, Rodríguez-Juárez F, Bellelli A, Gnaiger E, Cadenas S (2010) Kinetic model of the inhibition of respiration by endogenous nitric oxide in intact cells. Biochim Biophys Acta. doi:10.1016/j.bbabio.2010.01.033

  18. Chance B, Williams GR (1955) Respiratory enzymes in oxidative phosphorylation. I. Kinetics of oxygen utilization. J Biol Chem 217:383–393

    PubMed  CAS  Google Scholar 

  19. Stadlmann S, Renner K, Pollheimer J, Moser PL, Zeimet AG, Offner FA, Gnaiger E (2006) Preserved coupling of oxidative phosphorylation but decreased mitochondrial respiratory capacity in IL-1β treated human peritoneal mesothelial cells. Cell Biochem Biophys 44:179–186

    Article  PubMed  CAS  Google Scholar 

  20. Smolková K, Bellance N, Scandurra F, Génot E, Gnaiger E, Plecitá-Hlavatá L, Ježek P, Rossignol R (2010) Mitochondrial bioenergetic adaptations of breast cancer cells to aglycemia and hypoxia. J Bioenerg Biomembr. doi:10.1007/s10863-009-9267-x

  21. Jones DP (1986) Intracellular diffusion gradients of O2 and ATP. Am J Physiol 250:C663–C675

    PubMed  CAS  Google Scholar 

  22. Villani G, Attardi G (1997) In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells. Proc Natl Acad Sci USA 94:1166–1171

    Article  PubMed  CAS  Google Scholar 

  23. Gnaiger E, Rieger G, Kuznetsov A, Fuchs A, Stadlmann S, Lassnig B, Hengster P, Eberl T, Margreiter R (1997) Mitochondrial ischemia-reoxygenation injury and plasma membrane integrity in human endothelial cells. Transplant Proc 29:3524–3526

    Article  PubMed  CAS  Google Scholar 

  24. Gnaiger E, Kuznetsov AV, Rieger G, Amberger A, Fuchs A, Stadlmann S, Eberl T, Margreiter R (2000) Mitochondrial defects by intracellular calcium overload versus endothelial cold ischemia/reperfusion injury. Transpl Int 13:555–557

    Google Scholar 

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

    PubMed  CAS  Google Scholar 

  26. Gnaiger E, Kuznetsov AV, Lassnig B, Fuchs A, Reck M, Renner K, Stadlmann S, Rieger G, Margreiter R (1998) High-resolution respirometry. Optimum permeabilization of the cell membrane by digitonin. In: Larsson C, Påhlman I-L, Gustafsson L (eds) Biothermokinetics in the post genomic era. Chalmers Reproservice, Göteborg, pp 89–95

    Google Scholar 

  27. Saks VA, Veksler VI, Kuznetsov AV, Kay L, Sikk P, Tiivel T, Tranqui L, Olivares J, Winkler K, Wiedemann F, Kunz WS (1998) Permeabilised cell and skinned fiber techniques in studies of mitochondrial function in vivo. Mol Cell Biochem 184:81–100

    Article  PubMed  CAS  Google Scholar 

  28. Kuznetsov AV, Schneeberger S, Seiler R, Brandacher G, Mark W, Steurer W, Saks V, Usson Y, Margreiter R, Gnaiger E (2004) Mitochondrial defects and heterogeneous cytochrome c release after cardiac cold ischemia and reperfusion. Am J Physiol Heart Circ Physiol 286:H1633–H1641

    Article  PubMed  CAS  Google Scholar 

  29. Kuznetsov AV, Strobl D, Ruttmann E, Königsrainer A, Margreiter R, Gnaiger E (2002) Evaluation of mitochondrial respiratory function in small biopsies of liver. Anal Biochem 305:186–194

    Article  PubMed  CAS  Google Scholar 

  30. Rasmussen UF, Rasmussen HN (2000) Human quadriceps muscle mitochondria: a functional characterization. Mol Cell Biochem 208:37–44

    Article  PubMed  CAS  Google Scholar 

  31. Palmer JW, Tandler B, Hoppel CL (1977) Biochemical properties of subsarcolemmal and interfibrillar mitochondria isolated from rat cardiac muscle. J Biol Chem 252:8731–8739

    PubMed  CAS  Google Scholar 

  32. Gnaiger E, Lassnig B, Kuznetsov AV, Margreiter R (1998) Mitochondrial respiration in the low oxygen environment of the cell: effect of ADP on oxygen kinetics. Biochim Biophys Acta 1365:249–254

    Article  PubMed  CAS  Google Scholar 

  33. Gnaiger E, Kuznetsov AV (2002) Mitochondrial respiration at low levels of oxygen and cytochrome c. Biochem Soc Trans 30:252–258

    Article  PubMed  CAS  Google Scholar 

  34. Scandurra FM, Gnaiger E (2010) Cell respiration under hypoxia: facts and artefacts in mitochondrial oxygen kinetics. Adv Exp Med Biol 662:7–25

    Article  PubMed  CAS  Google Scholar 

  35. Dubowitz V, Sewry CA (2006) Muscle biopsy: a practical approach. Saunders Elsevier, Philadelphia

    Google Scholar 

  36. Dufour S, Rousse N, Canioni P, Diolez P (1996) Top-down control analysis of temperature effect on oxidative phosphorylation. Biochem J 314:743–751

    PubMed  CAS  Google Scholar 

  37. Gnaiger E (ed) (2007) Mitochondrial pathways and respiratory control. OROBOROS MiPNet, Innsbruck. http://www.oroboros.at

  38. Sun F, Huo X, Zhai Y, Wang A, Xu J, Su D, Bartlam M, Rao Z (2005) Crystal structure of mitochondrial respiratory membrane protein Complex II. Cell 121:1043–1057

    Article  PubMed  CAS  Google Scholar 

  39. Puchowicz MA, Varnes ME, Cohen BH, Friedman NR, Kerr DS, Hoppel CL (2004) Oxidative phosphorylation analysis: assessing the integrated functional activity of human skeletal muscle mitochondria – case studies. Mitochondrion 4:377–385

    Article  PubMed  CAS  Google Scholar 

  40. Delhumeau G, Cruz-Mendoza AM, Lojero CG (1994) Protection of cytochrome c oxidase against cyanide inhibition by pyruvate and α-ketoglutarate: effect of aeration in vitro. Toxicol Appl Pharmacol 126:345–351

    Article  PubMed  CAS  Google Scholar 

  41. Boushel R, Gnaiger E, Schjerling P, Skovbro M, Kraunsøe R, Dela F (2007) Patients with type 2 diabetes have normal mitochondrial function in skeletal muscle. Diabetologia 50:790–796

    Article  PubMed  CAS  Google Scholar 

  42. Gnaiger E, Wright-Paradis C, Sondergaard H et al (2005) High-resolution respirometry in small biopsies of human muscle: correlations with body mass index and age. Mitochondr Physiol Netw 10(9):14–15. http://www.mitophysiology.org/index.php?gnaigere

    Google Scholar 

  43. Scheibye-Knudsen M, Quistorff B (2009) Regulation of mitochondrial respiration by inorganic phosphate; comparing permeabilized muscle fibers and isolated mitochondria prepared from type-1 and type-2 rat skeletal muscle. Eur J Appl Physiol 105:279–287

    Article  PubMed  CAS  Google Scholar 

  44. Aragonés J, Schneider M, Van Geyte K et al (2008) Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolism. Nat Genet 40:170–180

    Article  PubMed  Google Scholar 

  45. Kuznetsov AV, Lassnig B, Margreiter R, Gnaiger E (1998) Diffusion limitation of oxygen versus ADP in permeabilized muscle fibers. In: Larsson C, Påhlman I-L, Gustafsson L (eds) Biothermokinetics in the post genomic era. Chalmers Reproservice, Göteborg, pp 273–276

    Google Scholar 

  46. Gnaiger E, Forstner H (eds) (1983) Polarographic oxygen sensors. aquatic and physiological applications. Springer, New York

    Google Scholar 

  47. Gnaiger E (2010) Oxygen calibration and solubility in experimental media. Mitochondr Physiol Netw 6(3):1–20. http://www.oroboros.at

    Google Scholar 

  48. Fasching M, Gnaiger E (2010) Instrumental background correction and accuracy of oxygen flux. Mitochondr Physiol Netw 14(6):1–12. http://www.oroboros.at

    Google Scholar 

  49. Kuznetsov AV, Veksler V, Gellerich FN, Saks V, Margreiter R, Kunz WS (2008) Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells. Nat Protoc 3:965–976

    Article  PubMed  CAS  Google Scholar 

  50. Gnaiger E, Steinlechner R, Keriel C, Leverve X, Rossi A, Saks V, Sibille B, Kay L, Novel V, Daneshrad Z, Gellerich FN, Eberl T, Skladal D, Sperl W, Margreiter R (1995) Oxygen sensitivity of respiration in endothelial cells, hepatocytes and permeabilized muscle fibers studied by high-resolution respirometry. J Mol Med 73:B39

    Google Scholar 

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Acknowledgments

This work was supported by OeNB Jubiläumsfond project 13476 and is a contribution to Mitofood COST Action FAO602. We thank Dr. Michael Schocke who was responsible for taking the human biopsies, and Drs. Robert Boushel, Flemming Dela, Steen Larson, Nis Stride, Dan Kane, and Darrel Neufer for advice in the technique of biopsy sampling.

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Correspondence to Erich Gnaiger .

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Pesta, D., Gnaiger, E. (2012). High-Resolution Respirometry: OXPHOS Protocols for Human Cells and Permeabilized Fibers from Small Biopsies of Human Muscle. In: Palmeira, C., Moreno, A. (eds) Mitochondrial Bioenergetics. Methods in Molecular Biology, vol 810. Humana Press. https://doi.org/10.1007/978-1-61779-382-0_3

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  • DOI: https://doi.org/10.1007/978-1-61779-382-0_3

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