Mitochondrial biogenesis in fast skeletal muscle of CK deficient mice

Biochimica et Biophysica Acta - Bioenergetics

Volumn 1777, Issue 1, 2008, Pages 39-47

  Vaarmann, A ^a,b,c   Fortin, D ^a,b   Veksler, V ^a,b   Momken, I ^a,b   Ventura Clapier, R ^a,b   Garnier, A ^a,b  

^a INSERM   (France)

^b UNIVERSITÉ PARIS SACLAY   (France)

^c UNIVERSITY OF TARTU   (Estonia)

Author keywords

AMPK; CK KO mice; Energy metabolism; Skeletal muscle; Transcription

Indexed keywords

CALCINEURIN; CITRATE SYNTHASE; CREATINE KINASE; CREATINE KINASE MM; CYTOCHROME C OXIDASE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE KINASE; MITOCHONDRIAL DNA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA COACTIVATOR 1ALPHA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA COACTIVATOR 1BETA; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR NRF2;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BIOGENESIS; CONTROLLED STUDY; CREATINE KINASE DEFICIENCY; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME DEFICIENCY; ENZYME REGULATION; ENZYME SUBUNIT; ENZYME SYNTHESIS; FAST MUSCLE FIBER; GASTROCNEMIUS MUSCLE; MITOCHONDRIAL MEMBRANE; MOUSE; MOUSE STRAIN; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; WILD TYPE;

ADENYLATE KINASE; ANIMALS; CREATINE KINASE; MICE; MICE, INBRED C57BL; MITOCHONDRIA, MUSCLE; MUSCLE, SKELETAL; SIGNAL TRANSDUCTION; TRANSCRIPTION, GENETIC;

MUS;

EID: 37549061787     PISSN: 00052728     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbabio.2007.11.003     Document Type: Article

References (47)

1. Qin W.N., Khuchua Z., Boero J., Payne R.M., and Strauss A.W. Oxidative myocytes of heart and skeletal muscle express abundant sarcomeric mitochondrial creatine kinase. Histochem. J. 31 (1999) 357-365
2. Ventura-Clapier R., Kuznetsov A., Veksler V., Boehm E., and Anflous K. Functional coupling of creatine kinases in muscles: species and tissue specificity. Mol. Cell. Biochem. 184 (1998) 231-247
3. van Deursen J., Heerschap A., Oerlemans F., Ruitenbeek W., Jap P., ter Laak H., and Wieringa B. Skeletal muscles of mice deficient in muscle creatine kinase lack burst activity. Cell 74 (1993) 621-631
4. Gorselink M., Drost M.R., Coumans W.A., van Kranenburg G.P., Hesselink R.P., and van der Vusse G.J. Impaired muscular contractile performance and adenine nucleotide handling in creatine kinase-deficient mice. Am. J. Physiol., Endocrinol Metabol. 281 (2001) E619-E625
5. Dahlstedt A.J., and Westerblad H. Inhibition of creatine kinase reduces the rate of fatigue-induced decrease in tetanic Ca(2+). J. Physiol. 533 (2001) 639-649
6. Veksler V.I., Kuznetsov A.V., Anflous K., Mateo P., van Deursen J., Wieringa B., and Ventura-Clapier R. Muscle creatine kinase-deficient mice.2. Cardiac and skeletal muscles exhibit tissue-specific adaptation of the mitochondrial function. J. Biol. Chem. 270 (1995) 19921-19929
7. Kaasik A., Veksler V., Boehm E., Novotova M., and Ventura-Clapier R. From energy store to energy channeling: a study in creatine kinase deficient fast skeletal muscle. FASEB J. 17 (2003) 708-710
8. Novotova M., Pavlovicova M., Veksler V., Ventura-Clapier R., and Zahradnik I. Ultrastructural remodeling of fast skeletal muscle fibers induced by invalidation of creatine kinase. Am. J. Physiol., Cell Physiol. 291 (2006) C1279-C1285
9. de Groof A.J., Smeets B., Groot Koerkamp M.J., Mul A.N., Janssen E.E., Tabak H.F., and Wieringa B. Changes in mRNA expression profile underlie phenotypic adaptations in creatine kinase-deficient muscles. FEBS Lett. 506 (2001) 73-78
10. de Groof A.J., Oerlemans F.T., Jost C.R., and Wieringa B. Changes in glycolytic network and mitochondrial design in creatine kinase-deficient muscles. Muscle Nerve 24 (2001) 1188-1196
11. Wu Z.D., Puigserver P., Andersson U., Zhang C.Y., Adelmant G., Mootha V., Troy A., Cinti S., Lowell B., Scarpulla R.C., and Spiegelman B.M. Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1. Cell 98 (1999) 115-124
12. Knutti D., and Kralli A. PGC-1, a versatile coactivator. Trends Endocrinol. Metab. 12 (2001) 360-365
13. Scarpulla R.C. Transcriptional activators and coactivators in the nuclear control of mitochondrial function in mammalian cells. Gene 286 (2002) 81-89
14. Larsson N.G., Wang J., Wilhelmsson H., Oldfors A., Rustin P., Lewandoski M., Barsh G.S., and Clayton D.A. Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice. Nat. Genet. 18 (1998) 231-236
15. Fluck M., and Hoppeler H. Molecular basis of skeletal muscle plasticity-from gene to form and function. Rev. Physiol., Biochem. Pharmacol. 146 (2003) 159-216
16. Reznick R.M., and Shulman G.I. The role of AMP-activated protein kinase in mitochondrial biogenesis. J. Physiol. 574 (2006) 33-39
17. Hood D.A., Irrcher I., Ljubicic V., and Joseph A.M. Coordination of metabolic plasticity in skeletal muscle. J. Exp. Biol. 209 (2006) 2265-2275
18. Garnier A., Fortin D., Zoll J., N'Guessan B., Mettauer B., Lampert E., Veksler V., and Ventura-Clapier R. Coordinated changes in mitochondrial function and biogenesis in healthy and diseased human skeletal muscle. FASEB J. 19 (2005) 43-52
19. Chin E.R., Olson E.N., Richardson J.A., Yang Q., Humphries C., Shelton J.M., Wu W., Bassel-Duby R., and Williams R.S. A calcineurin-dependent transcriptional pathway controls skeletal muscle fiber type. Genes Dev. 12 (1998) 2499-2509
20. Lin J., Wu H., Tarr P.T., Zhang C.Y., Wu Z., Boss O., Michael L.F., Puigserver P., Isotani E., Olson E.N., Lowell B.B., Bassel-Duby R., and Spiegelman B.M. Transcriptional co-activator PGC-1alpha drives the formation of slow-twitch muscle fibres. Nature 418 (2002) 797-801
21. Garcia-Roves P.M., Huss J., and Holloszy J.O. Role of calcineurin in exercise-induced mitochondrial biogenesis. Am. J. Physiol., Endocrinol Metab. 290 (2006) E1172-E1179
22. Bigard X., Sanchez H., Zoll J., Mateo P., Rousseau V., Veksler V., and Ventura-Clapier R. Calcineurin co-regulates contractile and metabolic components of slow muscle phenotype. J. Biol. Chem. 275 (2000) 19653-19660
23. Akimoto T., Pohnert S.C., Li P., Zhang M., Gumbs C., Rosenberg P.B., Williams R.S., and Yan Z. Exercise stimulates Pgc-1alpha transcription in skeletal muscle through activation of the p38 MAPK pathway. J. Biol. Chem. 280 (2005) 19587-19593
24. Wu H., Kanatous S.B., Thurmond F.A., Gallardo T., Isotani E., Bassel-Duby R., and Williams R.S. Regulation of mitochondrial biogenesis in skeletal muscle by CaMK. Science 296 (2002) 349-352
25. Bergeron R., Ren J.M., Cadman K.S., Moore I.K., Perret P., Pypaert M., Young L.H., Semenkovich C.F., and Shulman G.I. Chronic activation of AMP kinase results in NRF-1 activation and mitochondrial biogenesis. Am. J. Physiol. 281 (2001) E1340-E1346
26. Zong H., Ren J.M., Young L.H., Pypaert M., Mu J., Birnbaum M.J., and Shulman G.I. AMP kinase is required for mitochondrial biogenesis in skeletal muscle in response to chronic energy deprivation. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 15983-15987
27. Jorgensen S.B., Wojtaszewski J.F., Viollet B., Andreelli F., Birk J.B., Hellsten Y., Schjerling P., Vaulont S., Neufer P.D., Richter E.A., and Pilegaard H. Effects of alpha-AMPK knockout on exercise-induced gene activation in mouse skeletal muscle. FASEB J. 19 (2005) 1146-1148
28. Garnier A., Fortin D., Delomenie C., Momken I., Veksler V., and Ventura-Clapier R. Depressed mitochondrial transcription factors and oxidative capacity in rat failing cardiac and skeletal muscles. J. Physiol. 551 (2003) 491-501
29. Choi Y.S., Lee H.K., and Pak Y.K. Characterization of the 5′-flanking region of the rat gene for mitochondrial transcription factor A (Tfam). Biochim. Biophys. Acta 1574 (2002) 200-204
30. Puigserver P., Wu Z., Park C.W., Graves R., Wright M., and Spiegelman B.M. A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis. Cell 92 (1998) 829-839
31. Wang Y.X., Zhang C.L., Yu R.T., Cho H.K., Nelson M.C., Bayuga-Ocampo C.R., Ham J., Kang H., and Evans R.M. Regulation of muscle fiber type and running endurance by PPARdelta. PLoS Biol. 2 (2004) e294
32. Wu H., Naya F.J., McKinsey T.A., Mercer B., Shelton J.M., Chin E.R., Simard A.R., Michel R.N., BasselDuby R., Olson E.N., and Williams R.S. MEF2 responds to multiple calcium-regulated signals in the control of skeletal muscle fiber type. EMBO J. 19 (2000) 1963-1973
33. Kaasik A., Veksler V., Boehm E., Novotova M., Minajeva A., and Ventura-Clapier R. Energetic crosstalk between organelles: architectural integration of energy production and utilization. Circ. Res. 89 (2001) 153-159
34. ter Veld F., Jeneson J.A., and Nicolay K. Mitochondrial affinity for ADP is twofold lower in creatine kinase knock-out muscles. Possible role in rescuing cellular energy homeostasis. FEBS J. 272 (2005) 956-965
35. Momken I., Lechene P., Koulmann N., Fortin D., Mateo P., Doan B.T., Hoerter J., Bigard X., Veksler V., and Ventura-Clapier R. Impaired voluntary running capacity of creatine kinase-deficient mice. J. Physiol. 565 (2005) 951-964
36. Scarpulla R.C. Nuclear activators and coactivators in mammalian mitochondrial biogenesis. Biochim. Biophys. Acta 1576 (2002) 1-14
37. Puigserver P., and Spiegelman B.M. Peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC-1 alpha): transcriptional coactivator and metabolic regulator. Endocr. Rev. 24 (2003) 78-90
38. Arany Z., He H., Lin J., Hoyer K., Handschin C., Toka O., Ahmad F., Matsui T., Chin S., Wu P.H., Rybkin I.I., Shelton J.M., Manieri M., Cinti S., Schoen F.J., Bassel-Duby R., Rosenzweig A., Ingwall J.S., and Spiegelman B.M. Transcriptional coactivator PGC-1 alpha controls the energy state and contractile function of cardiac muscle. Cell Metab. 1 (2005) 259-271
39. Leone T.C., Lehman J.J., Finck B.N., Schaeffer P.J., Wende A.R., Boudina S., Courtois M., Wozniak D.F., Sambandam N., Bernal-Mizrachi C., Chen Z., Holloszy J.O., Medeiros D.M., Schmidt R.E., Saffitz J.E., Abel E.D., Semenkovich C.F., and Kelly D.P. PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis. PLoS Biol. 3 (2005) 101
40. Lin J., Handschin C., and Spiegelman B.M. Metabolic control through the PGC-1 family of transcription coactivators. Cell Metab. 1 (2005) 361-370
41. Luquet S., Lopez-Soriano J., Holst D., Fredenrich A., Melki J., Rassoulzadegan M., and Grimaldi P.A. Peroxisome proliferator-activated receptor delta controls muscle development and oxidative capability. FASEB J. 17 (2003) 2299-2301
42. Puigserver P., Rhee J., Lin J., Wu Z., Yoon J.C., Zhang C.Y., Krauss S., Mootha V.K., Lowell B.B., and Spiegelman B.M. Cytokine stimulation of energy expenditure through p38 MAP kinase activation of PPARgamma coactivator-1. Mol. Cell. 8 (2001) 971-982
43. Fan M., Rhee J., St-Pierre J., Handschin C., Puigserver P., Lin J., Jaeger S., Erdjument-Bromage H., Tempst P., and Spiegelman B.M. Suppression of mitochondrial respiration through recruitment of p160 myb binding protein to PGC-1alpha: modulation by p38 MAPK. Genes Dev. 18 (2004) 278-289
44. Jorgensen S.B., Richter E.A., and Wojtaszewski J.F. Role of AMPK in skeletal muscle metabolic regulation and adaptation in relation to exercise. J. Physiol. 574 (2006) 17-31
45. Atherton P.J., Babraj J., Smith K., Singh J., Rennie M.J., and Wackerhage H. Selective activation of AMPK-PGC-1alpha or PKB-TSC2-mTOR signaling can explain specific adaptive responses to endurance or resistance training-like electrical muscle stimulation. FASEB J. 19 (2005) 786-788
46. Jager S., Handschin C., St-Pierre J., and Spiegelman B.M. AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1{alpha}. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 12017-12022
47. Aguilar V., Alliouachene S., Sotiropoulos A., Sobering A., Athea Y., Djouadi F., Miraux S., Thiaudiere E., Foretz M., Viollet B., Diolez P., Bastin J., Benit P., Rustin P., Carling D., Sandri M., Ventura-Clapier R., and Pende M. S6 kinase deletion suppresses muscle growth adaptations to nutrient availability by activating AMP kinase. Cell Metab. 5 (2007) 476-487