Crystalline mitochondrial inclusion bodies isolated from creatine depleted rat soleus muscle

Journal of Cell Science

Volumn 110, Issue 12, 1997, Pages 1403-1411

  O'Gorman, Eddie ^a,b   Fuchs, Karl Hermann ^b   Tittmann, Peter ^b   Gross, Heinz ^b   Wallimann, Theo ^b  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b ETH ZURICH   (Switzerland)

Author keywords

Creatine kinase; Crystal; Inclusion body; Mitochondrion; Oxidative phosphorylation

Indexed keywords

CREATINE; CREATINE KINASE; GUANIDINOPROPIONIC ACID; MITOCHONDRIAL ENZYME; MUSCLE ENZYME;

ANIMAL TISSUE; ARTICLE; CELL INCLUSION; MUSCLE MITOCHONDRION; NONHUMAN; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL; RAT; SOLEUS MUSCLE;

ADENYLATE KINASE; ANIMALS; BRAIN; CELL RESPIRATION; CREATINE; CREATINE KINASE; CRYSTALLIZATION; INCLUSION BODIES; KIDNEY; LIVER; MICROSCOPY, ELECTRON; MITOCHONDRIA, MUSCLE; MUSCLE, SKELETAL; MYOCARDIUM; RATS; RATS, SPRAGUE-DAWLEY; TIME FACTORS; TISSUE DISTRIBUTION;

ANIMALIA;

EID: 0030857659     PISSN: 00219533     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (37)

1. Attardi, G. and Shatz, G. (1988). Biogenesis of mitochondria. Annu. Rev. Cell Biol. 4, 289-333.
2. Brdiczka, D., Kaldis, P. and Wallimann, T. (1994). In vitro complex formation between the octamer of mitochondrial creatine kinase and porin. J. Biol. Chem. 269, 27640-27644.
3. Boehm, E. A., Radda, G. K., Tomlin, H. and Clark, J. F. (1996). The utilization of creatine and its analogues by cytosolic and mitochondrial creatine kinase. Biochim. Biophys. Acta. 1274, 119-128.
4. Bücher, T., Luh, W. and Pette, D. (1964). Einfach und zusammengestze optische Tests mit Pyridininucleotiden. In Hoppe-Seyler and Thierfelder Handbuch der Physiologisch- und Pathologisch-chemischen Annalyse (ed. K. Lang and E. Lehrartz), vol. VIA. pp. 293-339. Springer: Berlin. Goettingen, Heidelberg.
5. Clark, J. F., Khuchua, Z., Kuznetzov, A. V., Vasssil'eva, E., Boehm, E., Radda, G. K. and Saks, V. (1994). Actions of the creatine analogue β-guanidinopropionic acid on rat heart mitochondria. Biochem. J. 300, 211-216.
6. DeTata, V., Cavallini, G., Pollera, M., Gori, Z. and Bergamini, E. (1993). The induction of mitochondrial myopathy in the rat by feeding beta-guanidinopropionic acid and the reversibility of the induced lesions: a biochemical and ultrastructural investigation. Int. J. Exp. Path. 74, 501-509.
7. Eppenberger-Erberhardt, M., Riesinger, I., Messerli, M., Schwarb, P., Müller, M., Eppenberger, H. M. and Wallimann, T. (1991). Adult rat cardiomyocytes cultured in creatine-deficient medium display large mitochondria with paracrystalline inclusions, enriched for creatine kinase. J. Cell Biol. 113, 289-300.
8. Farrants, G. W., Hovmöller, S. and Stadhouders, A. D. M. (1988). Two types of mitochondrial crystals in diseased human skeletal muscle fibres. Muscle & Nerve. 11, 45-55.
9. Freyssenet, D., Berthon, P., Geyssant, A. and Denis, C. (1994). ATP synthesis kinetic properties of mitochondria isolated from the rat extensor digitorum longus muscle depleted of creatine with beta guanidinopropionic acid. Biochim. Biophys. Acta. 1186, 232-236.
10. Fritz-Wolf, K., Schnyder, T., Wallimann, T. and Kabsch, W. (1996). Structure of mitochondrial creatine kinase. Nature 381, 341-345.
11. Hagenfeldt, L., Döbeln, U., Solders, G. and Kaijser, L. (1994). Creatine treatment in MELAS. Muscle & Nerve 17, 1238.
12. Hanzlikova, V. and Schiaffino, S. (1977). Mitochondrial changes in ischemic skeletal muscle. J. Ultrastuct. Res. 60, 121-133.
13. Johns, D. R. (1996). The other human genome: Mitochondrial DNA and disease. Nature Med. 2, 1065-1068.
14. Karpati, G., Carpenter S., Melmed, C. and Eisen, A. A. (1974). Experimental ischemic myopathy. J. Neurol. Sci. 23, 129-161.
15. Klein, S. C., Haas, R. C., Perrymann, M. B., Billadello, J. J. and Strauss, A. W. (1991). Regulatory element analysis and structural characterization of the human sarcomeric mitochondrial creatine kinase gene. J. Biol. Chem. 266, 18058-18065.
16. Laemmli, U. K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 1133-1142.
17. Moerland, T. S., Wolf, N. G. and Kushmerick, M. J. (1989). Administration of a creatine analogue induces myosin transitions in muscle. Am. J. Physiol. 257, C810-C816.
18. O'Gorman, E., Beutner, G., Wallimann, T. and Brdiczka, D. (1996). Differential effects of creatine depletion on the regulation of enzyme activities and on creatine-stimulated mitochondrial respiration in skeletal muscle, heart and brain. Biochim. Biophys. Acta. 1276, 161-170.
19. Ohira, Y., Kanzaki, M. and Chen, C. S. (1988). Intramitochondrial inclusions caused by depletion of creatine in rat skeletal muscles. Jap. J. Physiol. 38, 159-166.
20. Ren, J. M. and Holloszy, J. O. (1992). Adaptation of rat skeletal muscle to creatine depletion: AMP deaminase and AMP deamination. J. Appl. Physiol. 73, 2713-2716.
21. Ren, J. M., Ohira, Y., Holloszy, J. O., Hämäläinen, N., Traub, I. and Pette, D. (1995). Effects of β-guanidinopropionic acid-feeding on the patterns of myosin isoforms in rat fast-twitch muscle. Eur. J. Physiol. 430, 389-393.
22. Rojo, M., Hovius, H., Demel, R. A., Nicolay, K. and Wallimann, T. (1991). Mitochondrial creatine kinase mediates contact formation between mitochondrial membranes. J. Biol. Chem. 226, 20290-20295.
23. Rowley, G. L., Greenleaf, A. L. and Kenyon, G. L. (1971). On the specificity of creatine kinase. New glycocyamines and glycocyamine analogs related to creatine. J. Am. Chem. Soc. 93, 5542-5551.
24. 2+ uptake and regulate local ATP/ADP ratios. J. Biol. Chem. 265, 5258-5266.
25. Saks, V. A., Rosenshtraukh, L. V., Smirnov, N. and Chazov, E. I. (1978). Role of creatine phosphokinase in cellular function and metabolism. Can. J. Physiol. Pharmacol. 56, 691-706.
26. Saxton, W. O. and Baumeister, W. (1982). Three-dimensional reconstruction of imperfect two-dimensional crystals. Ultramicroscopy 13, 57-70.
27. Schlegel, J., Zurbriggen, B., Wegmann, G., Wyss, M., Eppenberger, H. M. and Wallimann, T. (1988). Isolation of two interconvertible mitochondrial creatine kinase forms, dimeric and octameric mitochondrial creatine kinase: characterisation, localisation, and structure-function relationships. J. Biol. Chem. 262, 16942-16593.
28. Schnyder, T., Cyrklaff, M., Fuchs, K. H. and Wallimann, T. (1994). Crystallisation of mitochondrial creatine kinase on negatively charged lipid layers. J. Struct. Biol. 112, 136-147.
29. Shoubridge, E. A., Challiss, R. A. J., Hayes, D. J. and Radda G. K. (1985). Biochemical adaptation in the skeletal muscle of rats depleted of creatine with the substrate analogue beta-guanidinopropionic acid. Biochem. J. 232, 125-131.
30. Stachowiak, O., Dolder, M. and Wallimann, T. (1996). Membrane-binding and lipid vesicle cross-linking kinetics of the creatine kinase octamer. Biochemistry 35, 15522-15528.
31. Stadhouders, A. M., Jap, P., Winkler, H. P., Eppenberger, H. M. and Wallimann T. (1994). Mitochondrial creatine kinase: A major constituent of pathological inclusions seen in mitochondrial myopathies. Proc. Nat. Acad. Sci. USA 91, 5089-5093.
32. Takahashi, M. and Hood, D. A. (1996). Protein import into subsarcolemmal and intermyofibrillar skeletal muscle mitochondria. J. Biol. Chem. 271, 27285-27291.
33. Taylor, D. J. and Radda G. K. (1994). Mitochondrial disease: noninvasive techniques. In Current Topics in Bioenergetics 17: Molecular Basis of Mitochondrial Pathology (ed. C. P. Lee), pp. 99-123. Academic Press, London.
34. Unser, M., Trus, B. L. and Steven, C. (1987). A new resolution criterion based on the spectral signal to noise ratios. Ultramicroscopy 23, 39-41.
35. Wallace, D. C. (1992). Diseases of mitochondrial genes. Annu. Rev. Biochem. 61, 1175-1212.
36. Wallimann, T., Schlösser, T. and Eppenberger, H. M. (1984). Function of M-line bound creatine kinase as intramyofibrillar ATP regenerator at the receiving end of the phosphorylcreatine shuttle in muscle. J. Biol. Chem. 209, 5238-5246.
37. Wallimann, T., Wyss, M., Brdiczka, D. and Nicolay, K. (1992). Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the 'phosphocreatine circuit' for cellular energy homeostasis. Biochem. J. 281, 21-40.