Acridine orange accumulation in acid organelles of normal and vacuolated frog skeletal muscle fibres

Cell Biology International

Volumn 30, Issue 11, 2006, Pages 933-939

  Krolenko, S A ^a   Adamyan, S Ya ^a   Belyaeva, T N ^a   Mozhenok, T P ^a  

^a INSTITUTE OF CYTOLOGY   (Russian Federation)

Author keywords

Acid organelles; Acridine orange; Confocal microscopy; Skeletal muscle; T system; Vacuolation

Indexed keywords

ACRIDINE ORANGE; GLYCEROL;

ACIDIFICATION; ANIMAL CELL; ARTICLE; CELL MEMBRANE; CELL NUCLEUS; CELL ORGANELLE; CELL VACUOLE; CONTROLLED STUDY; FROG; GOLGI COMPLEX; GRANULE CELL; LYSOSOME; MUSCLE CELL; MUSCLE FIBRIL; NONHUMAN; SCINTISCANNING; SKELETAL MUSCLE; STAINING; TRANSVERSE TUBULAR SYSTEM;

ACRIDINE ORANGE; AMINES; ANIMALS; ANURA; BORON COMPOUNDS; CERAMIDES; CYTOPLASMIC GRANULES; MONENSIN; MUSCLE FIBERS; MUSCLE, SKELETAL; ORGANELLES; SPECTROMETRY, FLUORESCENCE; STAINING AND LABELING; VACUOLES;

ANURA;

EID: 33750374594     PISSN: 10656995     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cellbi.2006.06.017     Document Type: Article

References (35)

1. Bechet D., Tassa A., Taillandier D., Combaret L., and Attaix D. Lysosomal proteolysis in skeletal muscle. Int J Biochem Cell Biol 37 (2005) 2098-2111
2. Bird I.W.C., Roisen F.J., Yorke G., Lee J.A., McElligott M.A., Triemer D.F., et al. Lysosomes and proteolytic enzyme activities in cultured striated musclecells. J Histochem Cytochem 29 (1981) 431-439
3. Brette F., and Orchard C. T-tubule function in mammalian cardiac myocytes. Circ Res 92 (2003) 1182-1192
4. Canonico P.G., and Bird J.W.G. The use of acridine orange as a lysosomal marker in rat skeletal muscle. J Cell Biol 43 (1969) 367-371
5. Clerc S., and Barenholz Y. A quantitative model for using acridine orange as a transmembrane pH gradient probe. Anal Biochem 259 (1998) 104-111
6. Cooper S.J., Chawla S., Fraser J.A., Skepper J.N., and Huang C.L. Separation of detubulation and vacuolation phenomena in amphibian skeletal muscle. J Muscle Res Cell Motil 3 (2002) 327-333
7. Devlin C.M., Chawla S., Skepper J.N., and Huang C.L.-H. Persistent tubular conduction in vacuolated amphibian skeletal muscle following osmotic shock. J Muscle Res Cell Motil 22 (2001) 459-466
8. Franzini-Armstrong C. Functional significance of membrane architecture in skeletal and cardiac muscle. Soc Gen Physiol Ser 51 (1996) 3-18
9. Gonzalez-Serratos H.G., Somlyo A.V., McClellan G., Shuman H., Borrero L., and Somlyo A.P. Composition of vacuoles and sarcoplasmic reticulum in fatigued muscle: electron probe analysis. Proc Natl Acad Sci U S A 75 (1978) 1329-1333
10. Haugland R.P. Handbook of fluorescent probes and research chemicals. 9th Ed. (2004), Molecular Probes, Eugene, OR, USA
11. Kaisto T., Rahkila P., Marjomäki V., Parton R.G., and Metsikkö K. Endocytosis in skeletal muscle fibers. Exp Cell Res 253 (1999) 551-560
12. Krolenko S.A., and Lucy J.A. Reversible vacuolation of T-tubules in skeletal muscle: mechanisms and implications for cell biology. Int Rev Cytol 202 (2001) 243-298
13. Krolenko S.A., and Lucy J.A. Vacuolation in T-tubules as a model for tubular-vesicular transformation in biomembrane system. Cell Biol Int 26 (2002) 893-904
14. Krolenko S.A., Amos W.B., and Lucy J.A. Reversible vacuolation of the transverse tubules of frog skeletal muscle: a confocal fluorescence microscopy study. J Muscle Res Cell Motil 16 (1995) 401-411
15. Krolenko S.A., Amos W.B., Brown S.C., Tarunina M.V., and Lucy J.A. Accessibility of T-tubule vacuoles to extracellular dextran and DNA: mechanism and potential application of vacuolation. J Muscle Res Cell Motil 19 (1998) 603-611
16. Lännergren J., Bruton J.D., and Westerblad H. Vacuole formation in fatigued muscle fibres from frog and mouse. J Muscle Res Cell Motil 20 (1999) 19-32
17. Lännergren J., Westerblad H., and Bruton J.D. Dynamic vacuolation in skeletal muscle fibres after fatigue. Cell Biol Int 26 (2002) 911-920
18. Launikonis B.S., and Stephenson D.G. Properties of the vertebrate skeletal muscle tubular system as a sealed compartment. Cell Biol Int 6 (2002) 921-929
19. Libelius R., Jirmanova I., Lundquist I., Thesleff S., and Barnard E.A. T-tubule endocytosis in dystrophic chicken muscle and its relation to muscle fiber degeneration. Acta Neuropathol 48 (1979) 31-38
20. Libelius R., Josefsson J.O., and Lundquist I. Endocytosis in chronically denervated mouse skeletal muscle. A biochemical and ultrastructural study with horseradish peroxidase. J Neurosci 4 (1979) 283-292
21. Lu Z., Joseph D., Bugnard E., Zaal K.J., and Ralston E. Golgi complex reorganization during muscle differentiation: visualization in living cells and mechanism. Mol Biol Cell 12 (2001) 795-808
22. McNeil P.L., and Steinhardt R.A. Loss, restoration, and maintenance of plasma membrane integrity. J Cell Biol 137 (1997) 1-4
23. Millot C., Millot J.M., Morjani H., Desplaces A., and Manfait M. Characterization of acidic vesicles in multidrug-resistant and sensitive cancer cells by acridine orange staining and confocal microspectrofluorometry. J Histochem Cytochem 45 (1997) 1255-1264
24. Mobley B.A., and Eisenberg B.R. Sizes of components in frog skeletal muscle measured by methods of stereology. J Gen Physiol 66 (1975) 31-45
25. Palmgren M.G. Acridine orange as a probe for measuring pH gradients across membranes: mechanism and limitations. Anal Biochem 192 (1991) 316-321
26. Rahkila P., Alakangas A., Väänänen K., and Metsikkö K. Transport pathway, maturation, and targetting of the vesicular stomatitus virus glycoprotein in skeletal muscle fibers. J Cell Sci 109 (1996) 1585-1596
27. Ralston E. Changes in architecture of the Golgi complex and other subcellular organelles during myogenesis. J Cell Biol 120 (1993) 399-409
28. Ralston E., Lu Z., and Ploug T. The organization of the Golgi complex and microtubules in skeletal muscle is fiber type-dependent. J Neurosci 19 (1999) 10694-10705
29. Ralston E., Ploug T., Kalhovde J., and Lomo T. Golgi complex, endoplasmic reticulum exit sites, and microtubules in skeletal muscle fibers are organized by patterned activity. J Neurosci 21 (2001) 875-883
30. 2+-regulated exocytosis of lysosomes. Cell 106 (2001) 157-169
31. Schindler M., Grabski S., Hoff E., and Simon S.M. Defective pH regulation in acidic compartments in human breast cancer cells (MCF-7) is normalized in adriamycin-resistant cells (MCF-7adr). Biochemistry 35 (1996) 2811-2817
32. Voigt T., and Dauber W. About the T-system in the myofibril-free sarcoplasm of the frog muscle fibre. Tissue Cell 36 (2004) 245-248
33. Vult von Steyern F., Josefsson J.O., Tågerud S., and Rhodamin B. A fluorescent-probe for acid organelles in denervated skeletal muscle. J Histochem Cytochem 44 (1996) 267-274
34. Weisz O.A. Acidification and protein traffic. Int Rev Cytol 226 (2003) 259-319
35. Zelenin A.V. Acridine orange as a probe for cell and molecular biology. Fluorescent and luminescent probes for biological activity (1999), Academic Press, London p. 117-35