Abstract
The junction between the T system and sarcoplasmic reticulum (SR) of frog skeletal muscle was examined in resting and contracting muscles. Pillars, defined as pairs of electron-opaque lines bounding an electron- lucent interior, were seen spanning the gap between T membrane and SR. Feet, defined previously in images of heavily stained preparations, appear with electron-opaque interiors and as such are distinct from the pillars studied here. Amorphous material was often present in the gap between T membrane and SR. Sometimes the amorphous material appeared as a thin line parallel to the membranes; sometimes it seemed loosely organized at the sites where feet have been reported. Resting single fibers contained 39 +/- 14.3 (mean +/- SD; n = 9 fibers) pillars/micrometer2 of tubule membrane. Single fibers, activated by a potassium-rich solution at 4 degrees C, contained 66 +/- 12.9 pillars/micrometer2 (n = 8) but fibers contracting in response to 2 mM caffeine contained 33 +/- 8.6/micrometer2 (n = 5). Pillar formation occurs when fibers are activated electrically, but not when calcium is released directly from the SR; and so we postulate that pillar formation is a step in excitation-contraction coupling.
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- Caputo C. The effect of low temperature on the excitation-contraction coupling phenomena of frog single muscle fibres. J Physiol. 1972 Jun;223(2):461–482. doi: 10.1113/jphysiol.1972.sp009858. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chandler W. K., Rakowski R. F., Schneider M. F. Effects of glycerol treatment and maintained depolarization on charge movement in skeletal muscle. J Physiol. 1976 Jan;254(2):285–316. doi: 10.1113/jphysiol.1976.sp011233. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisenberg B. R., Gilai A. Structural changes in single muscle fibers after stimulation at a low frequency. J Gen Physiol. 1979 Jul;74(1):1–16. doi: 10.1085/jgp.74.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisenberg B. R., Mathias R. T., Gilai A. Intracellular localization of markers within injected or cut frog muscle fibers. Am J Physiol. 1979 Jul;237(1):C50–C55. doi: 10.1152/ajpcell.1979.237.1.C50. [DOI] [PubMed] [Google Scholar]
- 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]
- Forbes M. S., Sperelakis N. Membrane systems in skeletal muscle of the lizard Anolis carolinensis. J Ultrastruct Res. 1980 Nov;73(2):245–261. doi: 10.1016/s0022-5320(80)90127-6. [DOI] [PubMed] [Google Scholar]
- Franzini-Armstrong C. Membrane particles and transmission at the triad. Fed Proc. 1975 Apr;34(5):1382–1389. [PubMed] [Google Scholar]
- Franzini-Armstrong C. Structure of sarcoplasmic reticulum. Fed Proc. 1980 May 15;39(7):2403–2409. [PubMed] [Google Scholar]
- Gordon A. M., Huxley A. F., Julian F. J. Tension development in highly stretched vertebrate muscle fibres. J Physiol. 1966 May;184(1):143–169. doi: 10.1113/jphysiol.1966.sp007908. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HILL A. V. The mechanics of active muscle. Proc R Soc Lond B Biol Sci. 1953 Mar 11;141(902):104–117. doi: 10.1098/rspb.1953.0027. [DOI] [PubMed] [Google Scholar]
- Julian F. J., Sollins M. R., Moss R. L. Sarcomere length non-uniformity in relation to tetanic responses of stretched skeletal muscle fibres. Proc R Soc Lond B Biol Sci. 1978 Jan 24;200(1138):109–116. doi: 10.1098/rspb.1978.0009. [DOI] [PubMed] [Google Scholar]
- Kelly D. E., Kuda A. M. Subunits of the triadic junction in fast skeletal muscle as revealed by freeze-fracture. J Ultrastruct Res. 1979 Aug;68(2):220–233. doi: 10.1016/s0022-5320(79)90156-4. [DOI] [PubMed] [Google Scholar]
- Kelly D. E. The fine structure of skeletal muscle triad junctions. J Ultrastruct Res. 1969 Oct;29(1):37–49. doi: 10.1016/s0022-5320(69)80054-7. [DOI] [PubMed] [Google Scholar]
- Makowski L., Caspar D. L., Phillips W. C., Goodenough D. A. Gap junction structures. II. Analysis of the x-ray diffraction data. J Cell Biol. 1977 Aug;74(2):629–645. doi: 10.1083/jcb.74.2.629. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mathias R. T., Levis R. A., Eisenberg R. S. Electrical models of excitation-contraction coupling and charge movement in skeletal muscle. J Gen Physiol. 1980 Jul;76(1):1–31. doi: 10.1085/jgp.76.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Merz W. A. Die Streckenmessung an gerichteten Strukturen im Mikroskop und ihre Anwendung zur Bestimmung von Oberflächen-Volumen-Relationen im Knochengewebe. Mikroskopie. 1968 Feb;22(5):132–142. [PubMed] [Google Scholar]
- Oschman J. L., Wall B. J. Calcium binding to intestinal membranes. J Cell Biol. 1972 Oct;55(1):58–73. doi: 10.1083/jcb.55.1.58. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Politoff A. L., Rose S., Pappas G. D. The calcium binding sites of synaptic vesicles of the frog sartorius neuromuscular junction. J Cell Biol. 1974 Jun;61(3):818–823. doi: 10.1083/jcb.61.3.818. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Sakai T., Geffner E. S., Sandow A. Caffeine contracture in muscle with disrupted transverse tubules. Am J Physiol. 1971 Mar;220(3):712–717. doi: 10.1152/ajplegacy.1971.220.3.712. [DOI] [PubMed] [Google Scholar]
- Schneider M. F., Chandler W. K. Voltage dependent charge movement of skeletal muscle: a possible step in excitation-contraction coupling. Nature. 1973 Mar 23;242(5395):244–246. doi: 10.1038/242244a0. [DOI] [PubMed] [Google Scholar]
- Simionescu N., Simionescu M. Galloylglucoses of low molecular weight as mordant in electron microscopy. II. The moiety and functional groups possibly involved in the mordanting effect. J Cell Biol. 1976 Sep;70(3):622–633. doi: 10.1083/jcb.70.3.622. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Somlyo A. V. Bridging structures spanning the junctioning gap at the triad of skeletal muscle. J Cell Biol. 1979 Mar;80(3):743–750. doi: 10.1083/jcb.80.3.743. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sommer J. R., Dolber P. C., Taylor I. Filipin-cholesterol complexes in the sarcoplasmic reticulum of frog skeletal muscle. J Ultrastruct Res. 1980 Sep;72(3):272–285. doi: 10.1016/s0022-5320(80)90064-7. [DOI] [PubMed] [Google Scholar]
- Sommer J. R., Wallace N. R., Junker J. The intermediate cisterna of the sarcoplasmic reticulum of skeletal muscle. J Ultrastruct Res. 1980 May;71(2):126–142. doi: 10.1016/s0022-5320(80)90101-x. [DOI] [PubMed] [Google Scholar]
- Spray T. L., Waugh R. A., Sommer J. R. Peripheral couplings in adult vertebrate skeletal muscle. Anatomical observations and functional implications. J Cell Biol. 1974 Jul;62(1):223–227. doi: 10.1083/jcb.62.1.223. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walker S. M., Schrodt G. R., Edge M. B. The density attached to the inside surface of the apposed sarcoplasmic reticular membrane in vertebrate cardiac and skeletal muscle fibres. J Anat. 1971 Feb;108(Pt 2):217–230. [PMC free article] [PubMed] [Google Scholar]
- Yoshioka T., Ohmori K., Sakai T. Ultrastructural features of the sarcoplasmic reticulum during rapid cooling contracture and tetanus in frog skeletal muscle. Jpn J Physiol. 1981;31(1):29–42. doi: 10.2170/jjphysiol.31.29. [DOI] [PubMed] [Google Scholar]
- Yu L. P., Hartt J. E., Podolsky R. J. Equatorial x-ray intensities and isometric force levels in frog sartorius muscle. J Mol Biol. 1979 Jul 25;132(1):53–67. doi: 10.1016/0022-2836(79)90495-9. [DOI] [PubMed] [Google Scholar]