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. 1973 May 1;57(2):261–277. doi: 10.1083/jcb.57.2.261

THE ULTRASTRUCTURE OF Z DISKS FROM WHITE, INTERMEDIATE, AND RED FIBERS OF MAMMALIAN STRIATED MUSCLES

R W D Rowe 1
PMCID: PMC2108976  PMID: 4696547

Abstract

The Z disk ultrastructure of white, intermediate, and red fibers from mammalian muscle is examined. Three models are proposed that explain the differences between the three types of Z disk. The three models are all based on the same concept, i.e., looping filaments from both sides of the Z disk. The differences between the models are in terms of the spatial relationships of adjacent loops within the Z disk. In the white fiber Z disk model all the loops from one side of the Z disk are on the same plane. In intermediate fibers there are two planes of loops from both sides of the Z disk, whereas in red fibers there are three planes of loops from both sides. The implications of these three structures are discussed in relation to known physiological differences between the fiber types.

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Selected References

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  1. FRANZINI-ARMSTRONG C., PORTER K. R. THE Z DISC OF SKELETAL MUSCLE FIBRILS. Z Zellforsch Mikrosk Anat. 1964;61:661–672. doi: 10.1007/BF00342617. [DOI] [PubMed] [Google Scholar]
  2. Gauthier G. F. On the relationship of ultrastructural and cytochemical features of color in mammalian skeletal muscle. Z Zellforsch Mikrosk Anat. 1969;95(3):462–482. doi: 10.1007/BF00995217. [DOI] [PubMed] [Google Scholar]
  3. Goldspink G. The proliferation of myofibrils during muscle fibre growth. J Cell Sci. 1970 Mar;6(2):593–603. doi: 10.1242/jcs.6.2.593. [DOI] [PubMed] [Google Scholar]
  4. Hirsch J. G., Fedorko M. E. Ultrastructure of human leukocytes after simultaneous fixation with glutaraldehyde and osmium tetroxide and "postfixation" in uranyl acetate. J Cell Biol. 1968 Sep;38(3):615–627. doi: 10.1083/jcb.38.3.615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. KNAPPEIS G. G., CARLSEN F. The ultrastructure of the Z disc in skeletal muscle. J Cell Biol. 1962 May;13:323–335. doi: 10.1083/jcb.13.2.323. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kelly D. E., Cahill M. A. Filamentous and matrix components of skeletal muscle Z-disks. Anat Rec. 1972 Apr;172(4):623–642. doi: 10.1002/ar.1091720403. [DOI] [PubMed] [Google Scholar]
  7. Kelly D. E. Models of muscle Z-band fine structure based on a looping filament configuration. J Cell Biol. 1967 Sep;34(3):827–840. doi: 10.1083/jcb.34.3.827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Landon D. N. The influence of fixation upon the fine structure of the Z-disk of rat striated muscle. J Cell Sci. 1970 Jan;6(1):257–276. doi: 10.1242/jcs.6.1.257. [DOI] [PubMed] [Google Scholar]
  9. MARKHAM R., HITCHBORN J. H., HILLS G. J., FREY S. THE ANATOMY OF THE TOBACCO MOSAIC VIRUS. Virology. 1964 Mar;22:342–359. doi: 10.1016/0042-6822(64)90025-x. [DOI] [PubMed] [Google Scholar]
  10. Macdonald R. D., Engel A. G. Observations on organization of Z-disk components and on rod-bodies of Z-disk origin. J Cell Biol. 1971 Feb;48(2):431–437. doi: 10.1083/jcb.48.2.431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Otsuki I., Masaki T., Nonomura Y., Ebashi S. Periodic distribution of troponin along the thin filament. J Biochem. 1967 Jun;61(6):817–819. doi: 10.1093/oxfordjournals.jbchem.a128619. [DOI] [PubMed] [Google Scholar]
  12. PAGE S. G., HUXLEY H. E. FILAMENT LENGTHS IN STRIATED MUSCLE. J Cell Biol. 1963 Nov;19:369–390. doi: 10.1083/jcb.19.2.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. PAGE S. FILAMENT LENGTHS IN RESTING AND EXCITED MUSCLES. Proc R Soc Lond B Biol Sci. 1964 Oct 27;160:460–466. doi: 10.1098/rspb.1964.0056. [DOI] [PubMed] [Google Scholar]
  14. REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. ROMANUL F. C. ENZYMES IN MUSCLE. I. HISTOCHEMICAL STUDIES OF ENZYMES IN INDIVIDUAL MUSCLE FIBERS. Arch Neurol. 1964 Oct;11:355–358. doi: 10.1001/archneur.1964.00460220017003. [DOI] [PubMed] [Google Scholar]
  16. Rack P. M., Westbury D. R. The effects of length and stimulus rate on tension in the isometric cat soleus muscle. J Physiol. 1969 Oct;204(2):443–460. doi: 10.1113/jphysiol.1969.sp008923. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Rosenbluth J. Obliquely striated muscle. 3. Contraction mechanism of Ascaris body muscle. J Cell Biol. 1967 Jul;34(1):15–33. doi: 10.1083/jcb.34.1.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Rowe R. W., Morton D. J. Faults in the square lattice of mammalian skeletal muscle Z-disks. J Cell Sci. 1971 Jul;9(1):139–145. doi: 10.1242/jcs.9.1.139. [DOI] [PubMed] [Google Scholar]
  19. Rowe R. W. Ultrastructure of the Z line of skeletal muscle fibers. J Cell Biol. 1971 Dec;51(3):674–685. doi: 10.1083/jcb.51.3.674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Schiaffino S., Hanzlíková V., Pierobon S. Relations between structure and function in rat skeletal muscle fibers. J Cell Biol. 1970 Oct;47(1):107–119. doi: 10.1083/jcb.47.1.107. [DOI] [PMC free article] [PubMed] [Google Scholar]

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