Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1969 Jul 1;42(1):46–67. doi: 10.1083/jcb.42.1.46

THE ULTRASTRUCTURE OF THE CAT MYOCARDIUM

II. Atrial Muscle

N Scott McNutt 1, Don W Fawcett 1
PMCID: PMC2107577  PMID: 5786989

Abstract

The ultrastructure of the cells specialized for contraction in the atrium and ventricle of young adult cats are compared. The cells specialized for conduction are not included. In addition to possessing distinctive atrial granules, the cells of the atrium are smaller in diameter (5–6 µ) than ventricular cells (10–12 µ) and have strikingly fewer T tubules. These latter differences are discussed in terms of their possible significance for the rate of conduction of the action potential. It is suggested that the very small number of T tubules in atrial cells may compensate for the small cell diameter, and thus permit rapid conduction of the action potential across the surface of the atrium. Coated dense vesicles found in association with the sarcoplasmic reticulum at the level of the Z line in ventricular muscle are more evident in atrial cells. In the virtual absence of T tubules in atrial cells, the sub-sarcolemmal cisternae of the sarcoplasmic reticulum are almost exclusively at the cell periphery. The ends of the cells and their processes in ventricular muscle are rectilinear with the interdigitated portions of the intercalated discs oriented transversely, whereas those of the atrium are often oblique to the myofilament axis. This difference may be related to the lower mechanical tension on atrial cells.

Full Text

The Full Text of this article is available as a PDF (3.1 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BARR L., DEWEY M. M., BERGER W. PROPAGATION OF ACTION POTENTIALS AND THE STRUCTURE OF THE NEXUS IN CARDIAC MUSCLE. J Gen Physiol. 1965 May;48:797–823. doi: 10.1085/jgp.48.5.797. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BURDETTE W. J., ASHFORD T. P. STRUCTURAL CHANGES IN THE HUMAN MYOCARDIUM FOLLOWING HYPOXIA. J Thorac Cardiovasc Surg. 1965 Aug;50:210–220. [PubMed] [Google Scholar]
  3. Blinks J. R. Convenient apparatus for recording contractions of isolated heart muscle. J Appl Physiol. 1965 Jul;20(4):755–757. doi: 10.1152/jappl.1965.20.4.755. [DOI] [PubMed] [Google Scholar]
  4. Braunwald E., Ross J., Jr, Sonnenblick E. H. Mechanisms of contraction of the normal and failing heart. N Engl J Med. 1967 Oct 19;277(16):853–contd. doi: 10.1056/NEJM196710192771605. [DOI] [PubMed] [Google Scholar]
  5. Carney J. A., Brown A. L., Jr An electron microscope study of canine cardiac myosin and some of its aggregates. J Cell Biol. 1966 Feb;28(2):375–389. doi: 10.1083/jcb.28.2.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Costantin L. L., Podolsky R. J. Calcium localization and the activation of striated muscle fibers. Fed Proc. 1965 Sep-Oct;24(5):1141–1145. [PubMed] [Google Scholar]
  7. Dallner G., Siekevitz P., Palade G. E. Biogenesis of endoplasmic reticulum membranes. I. Structural and chemical differentiation in developing rat hepatocyte. J Cell Biol. 1966 Jul;30(1):73–96. doi: 10.1083/jcb.30.1.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Eisenberg R. S., Gage P. W. Frog skeletal muscle fibers: changes in electrical properties after disruption of transverse tubular system. Science. 1967 Dec 29;158(3809):1700–1701. doi: 10.1126/science.158.3809.1700. [DOI] [PubMed] [Google Scholar]
  9. FARQUHAR M. G., PALADE G. E. Junctional complexes in various epithelia. J Cell Biol. 1963 May;17:375–412. doi: 10.1083/jcb.17.2.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. FAWCETT D. W., SELBY C. C. Observations on the fine structure of the turtle atrium. J Biophys Biochem Cytol. 1958 Jan 25;4(1):63–72. doi: 10.1083/jcb.4.1.63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. FAWCETT D. W. The sarcoplasmic reticulum of skeletal and cardiac muscle. Circulation. 1961 Aug;24:336–348. doi: 10.1161/01.cir.24.2.336. [DOI] [PubMed] [Google Scholar]
  12. Farquhar M. G., Palade G. E. Cell junctions in amphibian skin. J Cell Biol. 1965 Jul;26(1):263–291. doi: 10.1083/jcb.26.1.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fawcett D. W., McNutt N. S. The ultrastructure of the cat myocardium. I. Ventricular papillary muscle. J Cell Biol. 1969 Jul;42(1):1–45. doi: 10.1083/jcb.42.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Fawcett D. W. The sporadic occurrence in cardiac muscle of anomalous Z bands exhibiting a periodic structure suggestive of tropomyosin. J Cell Biol. 1968 Jan;36(1):266–270. doi: 10.1083/jcb.36.1.266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Flickinger C., Fawcett D. W. The junctional specializations of Sertoli cells in the seminiferous epithelium. Anat Rec. 1967 Jun;158(2):207–221. doi: 10.1002/ar.1091580210. [DOI] [PubMed] [Google Scholar]
  16. Freygang W. H., Jr Tubular ionic movements. Fed Proc. 1965 Sep-Oct;24(5):1135–1140. [PubMed] [Google Scholar]
  17. Gage P. W., Eisenberg R. S. Action potentials without contraction in frog skeletal muscle fibers with disrupted transverse tubules. Science. 1967 Dec 29;158(3809):1702–1703. doi: 10.1126/science.158.3809.1702. [DOI] [PubMed] [Google Scholar]
  18. HASSELBACH W. RELAXATION AND THE SARCOTUBULAR CALCIUM PUMP. Fed Proc. 1964 Sep-Oct;23:909–912. [PubMed] [Google Scholar]
  19. HODGE A. J., HUXLEY H. E., SPIRO D. Electron microscope studies on ultrathin sections of muscle. J Exp Med. 1954 Feb;99(2):201–206. doi: 10.1084/jem.99.2.201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. HUXLEY H. E. The double array of filaments in cross-striated muscle. J Biophys Biochem Cytol. 1957 Sep 25;3(5):631–648. doi: 10.1083/jcb.3.5.631. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Hoyle G. Diversity of striated muscle. Am Zool. 1967 Aug;7(3):435–449. doi: 10.1093/icb/7.3.435. [DOI] [PubMed] [Google Scholar]
  22. JAMIESON J. D., PALADE G. E. SPECIFIC GRANULES IN ATRIAL MUSCLE CELLS. J Cell Biol. 1964 Oct;23:151–172. doi: 10.1083/jcb.23.1.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Johnson E. A., Sommer J. R. A strand of cardiac muscle. Its ultrastructure and the electrophysiological implications of its geometry. J Cell Biol. 1967 Apr;33(1):103–129. doi: 10.1083/jcb.33.1.103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. KARRER H. E. The striated musculature of blood vessels. I. General cell morphology. J Biophys Biochem Cytol. 1959 Dec;6:383–392. doi: 10.1083/jcb.6.3.383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. KARRER H. E. The striated musculature of blood vessels. II. Cell interconnections and cell surface. J Biophys Biochem Cytol. 1960 Sep;8:135–150. doi: 10.1083/jcb.8.1.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. KISCH B. A SGINIFICANT ELECTRON MICROSCOPIC DIFFERENCE BETWEEN THE ATRIA AND THE VENTRICLES OF THE MAMMALIAN HEART. Exp Med Surg. 1963;21:193–221. [PubMed] [Google Scholar]
  27. 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]
  28. 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]
  29. LINDNER E. Die submikroskopische Morphologie des Herzmuskels. Z Zellforsch Mikrosk Anat. 1957;45(6):702–746. [PubMed] [Google Scholar]
  30. Leak L. V. The ultrastructure of myofibers in a reptilian heart: the boa constrictor. Am J Anat. 1967 May;120(3):553–581. doi: 10.1002/aja.1001200308. [DOI] [PubMed] [Google Scholar]
  31. MOORE D. H., RUSKA H. Electron microscope study of mammalian cardiac muscle cells. J Biophys Biochem Cytol. 1957 Mar 25;3(2):261–268. doi: 10.1083/jcb.3.2.261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. MUIR A. R. An electron microscope study of the embryology of the intercalated disc in the heart of the rabbit. J Biophys Biochem Cytol. 1957 Mar 25;3(2):193–202. doi: 10.1083/jcb.3.2.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. NELSON D. A., BENSON E. S. On the structural continuities of the transverse tubular system of rabbit and human myocardial cells. J Cell Biol. 1963 Feb;16:297–313. doi: 10.1083/jcb.16.2.297. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. NIEDERGERKE R. Calcium and the activation of contraction. Experientia. 1959 Apr 15;15(4):128–130. doi: 10.1007/BF02165519. [DOI] [PubMed] [Google Scholar]
  35. PORTER K. R., PALADE G. E. Studies on the endoplasmic reticulum. III. Its form and distribution in striated muscle cells. J Biophys Biochem Cytol. 1957 Mar 25;3(2):269–300. doi: 10.1083/jcb.3.2.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. PUECH P., ESCLAVISSAT M., SODI-PALLARES D., CISNEROS F. Normal auricular activation in the dog's heart. Am Heart J. 1954 Feb;47(2):174–191. doi: 10.1016/0002-8703(54)90248-3. [DOI] [PubMed] [Google Scholar]
  37. Peachey L. D. The role of transverse tubules in excitation contraction coupling in striated muscles. Ann N Y Acad Sci. 1966 Jul 14;137(2):1025–1037. doi: 10.1111/j.1749-6632.1966.tb50214.x. [DOI] [PubMed] [Google Scholar]
  38. Peachey L. D. The sarcoplasmic reticulum and transverse tubules of the frog's sartorius. J Cell Biol. 1965 Jun;25(3 Suppl):209–231. doi: 10.1083/jcb.25.3.209. [DOI] [PubMed] [Google Scholar]
  39. Pepe F. A. The myosin filament. I. Structural organization from antibody staining observed in electron microscopy. J Mol Biol. 1967 Jul 28;27(2):203–225. doi: 10.1016/0022-2836(67)90016-2. [DOI] [PubMed] [Google Scholar]
  40. REVEL J. P., NAPOLITANO L., FAWCETT D. W. Identification of glycogen in electron micrographs of thin tissue sections. J Biophys Biochem Cytol. 1960 Dec;8:575–589. doi: 10.1083/jcb.8.3.575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. ROSENBLUTH J. Subsurface cisterns and their relationship to the neuronal plasma membrane. J Cell Biol. 1962 Jun;13:405–421. doi: 10.1083/jcb.13.3.405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. ROSENBLUTH J., WISSIG S. L. THE DISTRIBUTION OF EXOGENOUS FERRITIN IN TOAD SPINAL GANGLIA AND THE MECHANISM OF ITS UPTAKE BY NEURONS. J Cell Biol. 1964 Nov;23:307–325. doi: 10.1083/jcb.23.2.307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. ROTH T. F., PORTER K. R. YOLK PROTEIN UPTAKE IN THE OOCYTE OF THE MOSQUITO AEDES AEGYPTI. L. J Cell Biol. 1964 Feb;20:313–332. doi: 10.1083/jcb.20.2.313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Rambourg A., Leblond C. P. Electron microscope observations on the carbohydrate-rich cell coat present at the surface of cells in the rat. J Cell Biol. 1967 Jan;32(1):27–53. doi: 10.1083/jcb.32.1.27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Rayns D. G., Simpson F. O., Bertaud W. S. Transverse tubule apertures in mammalian myocardial cells: surface array. Science. 1967 May 5;156(3775):656–657. doi: 10.1126/science.156.3775.656. [DOI] [PubMed] [Google Scholar]
  46. SIMPSON F. O., OERTELIS S. J. The fine structure of sheep myocardial cells; sarcolemmal invaginations and the transverse tubular system. J Cell Biol. 1962 Jan;12:91–100. doi: 10.1083/jcb.12.1.91. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. SJOSTRAND F. S., ANDERSSON-CEDERGREN E., DEWEY M. M. The ultrastructure of the intercalated discs of frog, mouse and guinea pig cardiac muscle. J Ultrastruct Res. 1958 Apr;1(3):271–287. doi: 10.1016/s0022-5320(58)80008-8. [DOI] [PubMed] [Google Scholar]
  48. SONNENBLICK E. H. Force-velocity relations in mammalian heart muscle. Am J Physiol. 1962 May;202:931–939. doi: 10.1152/ajplegacy.1962.202.5.931. [DOI] [PubMed] [Google Scholar]
  49. SPIRO D., SONNENBLICK E. H. COMPARISON OF THE ULTRASTRUCTURAL BASIS OF THE CONTRACTILE PROCESS IN HEART AND SKELETAL MUSCLE. Circ Res. 1964 Nov;15:SUPPL 2–2:37. [PubMed] [Google Scholar]
  50. Sommer J. R., Johnson E. A. Cardiac muscle. A comparative study of Purkinje fibers and ventricular fibers. J Cell Biol. 1968 Mar;36(3):497–526. doi: 10.1083/jcb.36.3.497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. TRAUTWEIN W., UCHIZONO K. ELECTRON MICROSCOPIC AND ELECTROPHYSIOLOGIC STUDY OF THE PACEMAKER IN THE SINO-ATRIAL NODE OF THE RABBIT HEART. Z Zellforsch Mikrosk Anat. 1963 Oct 8;61:96–109. doi: 10.1007/BF00341523. [DOI] [PubMed] [Google Scholar]
  52. VANDERKLOOT W. G., DANE B. CONDUCTION OF THE ACTION POTENTIAL IN THE FROG VENTRICLE. Science. 1964 Oct 2;146(3640):74–75. doi: 10.1126/science.146.3640.74. [DOI] [PubMed] [Google Scholar]
  53. VENABLE J. H., COGGESHALL R. A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY. J Cell Biol. 1965 May;25:407–408. doi: 10.1083/jcb.25.2.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. WEBER A., HERZ R., REISS I. THE REGULATION OF MYOFIBRILLAR ACTIVITY BY CALCIUM. Proc R Soc Lond B Biol Sci. 1964 Oct 27;160:489–501. doi: 10.1098/rspb.1964.0063. [DOI] [PubMed] [Google Scholar]
  55. WEIDMANN S. The electrical constants of Purkinje fibres. J Physiol. 1952 Nov;118(3):348–360. doi: 10.1113/jphysiol.1952.sp004799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. WINEGRAD S. AUTORADIOGRAPHIC STUDIES OF INTRACELLULAR CALCIUM IN FROG SKELETAL MUSCLE. J Gen Physiol. 1965 Jan;48:455–479. doi: 10.1085/jgp.48.3.455. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. WINEGRAD S., SHANES A. M. Calcium flux and contractility in guinea pig atria. J Gen Physiol. 1962 Jan;45:371–394. doi: 10.1085/jgp.45.3.371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Winegrad S. Intracellular calcium movements of frog skeletal muscle during recovery from tetanus. J Gen Physiol. 1968 Jan;51(1):65–83. doi: 10.1085/jgp.51.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES