With scanning electron microscopy (SEM), highly organized parallel rows of pairs of openings corresponding to the level of the transverse tubular (T) system were seen on the surface of the muscle from normal mice and humans. The openings, usually round, were always found at the level of the A-I junction and varied from 500 to 1,500 Angstroms in diameter. Disappearance of the T system openings and the A-I banding pattern occurred in focal areas of both dystrophic and neurogenic atrophic fibers in the early stage.The results from scanning and transmission electron microscopy, and the preparation of specimen\p=m-\ofSEM are discussed. (28:247-251, 1973) In 1957 Porter and Palade1 de¬ scribed the fine structure of the triads in vertebrate muscle fibers consisting of one tubule of the trans¬ verse tubular (T) system and two elements of sarcoplasmic reticulum (SR). After Huxley and Taylor2 pub¬ lished their study on "local activation of striated muscle fibers," experi¬ ments were made with fluorescent dye and tritiated serum albumin and ferritin, the results of which suggest¬ ed a continuity between the lumen of the system and the extracellular space.37 Morphological observations on the system openings have been made by Franzini-Armstrong and Porter" and others911; however, be-cause of the complex nature of the involuting system, transmission electron microscopy (TEM) has failed to indicate the number of system openings per unit surface area. Scan¬ ning electron microscopic (SEM) ob¬ servations revealed the arrangement of the system openings on the sur¬ face of the striated muscle of frogs.12This report aims to reveal the sur¬ face structure of the striated muscle in normal and abnormal mice and humans by SEM and TEM. Problems are discussed in the preparation, es¬ pecially in fixation, of muscle speci¬ mens for SEM.
Materials and MethodsSkeletal muscles were obtained by biop¬ sy from normal mice and humans, dys¬ trophic mice, and patients with progres¬ sive muscular dystrophy and peripheral neuropathy due to multiple myeloma. The muscles to be biopsied were exposed and pinched by forked forceps to stretch the fibers to 100% to 120% of their resting length. The muscles were then washed by a gentle jet of normal saline,13 dissected, and fixed in two different ways. One was fixed for only one hour at 4C in 3% glutaraldehyde; the other was postfixed in 1% osmium tetraoxide (0,04) at 4C for an ad¬ ditional hour. After fixation the tissues were rinsed in distilled water and then rapidly dehydrated in a graded series of cold acetone baths. The dehydrated mus¬ cles were air-dried for 24 hours in a vacu¬ um desiccator containing a drying agent.The connective tissues of the muscle sur¬ face were removed by microtweezers un¬ der the binocular loupe. Observation and photography were made with a scanning electron microscope with an accelerative voltage of 15 kv.For transmission electron microscopy, the muscles were fixed at 4C for one hour Fig 1.-Transmission electron micrograph of normal striated muscle. Arrows indicate tu¬ bule...