Abstract
Muscle cells in the left ventricular walls of four markedly hypertrophied human hearts (above 600 gm) were compared with muscle cells in four non-hypertrophied hearts (up to 310 gm). Blocks of tissue obtained postmortem within 6 hours were processed for light and electron microscopy under conditions suitable for good preservation of myofibrils. A lattice parameter, qh, was defined as the number of myosin filaments per square micron in either H zones or A bands. By the use of methods of electron microscopy, qh was determined for perpendicular cross-sections of A bands in a large number of well preserved myofibrils of muscle cells in both groups of hearts. Statistical evaluation of the distributions of values of qh revealed no significant difference between the two groups. Thus, the myofilament lattices in hypertrophied cells were geometrically within normal limits. Planimetric measurements of cross-sectional areas of muscle fibers were made, using photomicrographs obtained from one representative hypertrophied heart and from one control. The size-frequency distribution of the measurements showed a marked difference between the two hearts, and confirmed the presence of hypertrophy of muscle cells. Counts of the number of myofibrils per muscle cell were determined for samples from the same two hearts, evaluated statistically, and found to be significantly higher for the hypertrophied heart. It is proposed (a) that myofibrils in hypertrophied heart muscle cells have filament lattices with geometrical arrangement and macromolecular parameters that are the same as those found in myofibrils of normal heart muscle cells; and (b) that in hypertrophy the number of myofilaments increases through formation of new myofibrils, and possibly also by addition of filaments to preexisting myofibrils.
Full Text
The Full Text of this article is available as a PDF (929.7 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- FARRANT J. L. An electron microscopic study of ferritin. Biochim Biophys Acta. 1954 Apr;13(4):569–576. doi: 10.1016/0006-3002(54)90376-5. [DOI] [PubMed] [Google Scholar]
- Karsner H. T., Saphir O., Todd T. W. The State of the Cardiac Muscle in Hypertrophy and Atrophy. Am J Pathol. 1925 Jul;1(4):351–372.1. [PMC free article] [PubMed] [Google Scholar]
- LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- OLSON R. E., ELLENBOGEN E., IYENGAR R. Cardiac myosin and congestive heart failure in the dog. Circulation. 1961 Aug;24:471–482. doi: 10.1161/01.cir.24.2.471. [DOI] [PubMed] [Google Scholar]
