Structural Unit of the Tissue
Unlike many other tissues, skeletal muscle is formed not by single cells, but by complex structures known as muscle fibers. The length of a single fiber ranges from several centimeters to tens of centimeters, usually corresponding to the anatomical length of the muscle itself.
Each muscle fiber comprises three essential components:
- Myosymplast. A long cylindrical structure forming the bulk and volume of the fiber. This is where the contractile apparatus resides.
- Myosatellite cells (satellite cells). Undifferentiated cells that serve as a stem cell reserve for growth and regeneration. They lie in specific depressions of the myosymplast plasmalemma but never fuse with it.
- Basal lamina. A universal external lamina that completely surrounds the myosymplast and myosatellite cell complex. In histology, the term sarcolemma is often used, which classically encompasses both the basal lamina and the plasmalemma.
Nuclear and Contractile Apparatus
Myosymplast morphology is best studied in longitudinal sections. A key feature of the tissue is the staggering number of nuclei per fiber. Approximately 95% of these are narrow, rod-shaped nuclei belonging to the myosymplast itself, while the remaining 5% belong to satellite cells. The myosymplast completely lacks cell centers (centrioles); therefore, its nuclei have lost the capacity for division under both normal conditions and injury.
Myosymplast nuclei are invariably pushed to the very periphery of the fiber. This is driven by the massive contractile apparatus—myofibrils—which occupy about 70% of the sarcoplasmic volume.
In high-magnification cross-sections, myofibrils appear as numerous dots (about 1,400 per fiber), each approximately 1.5 µm in diameter. Under light microscopy, they create the characteristic cross-striation of the entire fiber due to the regular alternation of light and dark bands (discs).
Tinctorial Properties and Microscopy
To comprehensively study tissue structure, histological preparations of the tongue are frequently used. In this organ, muscle bundles run in three mutually perpendicular directions, allowing multiple projections to be observed on a single histological slide: as longitudinal long tracts and as rounded cross-sections.
With standard hematoxylin and eosin (H&E) staining, muscle fibers display marked oxyphilia—their cytoplasm stains bright pink with eosin. This is due to the extremely high concentration of proteins in the sarcoplasm. For the clearest visualization of cross-striations, iron hematoxylin staining is applied.
Contraction Mechanism and Energy Supply
The function of skeletal muscle is based on the sliding filament theory. Contraction occurs not through the physical shortening of the protein molecules themselves, but as a result of changes in the degree of overlap between thin and thick myofilaments. The filaments slide past one another due to the cyclic attachment and detachment of cross-bridges. This brings the Z-lines closer together, shortens the sarcomere, and consequently shortens the entire myofibril.
This process is triggered by a nerve impulse that causes a sharp increase in calcium ion ($Ca^{2+}$) concentration in the sarcoplasm. Such high-energy activity requires a robust life-support system:
- Organelles: an extremely high density of mitochondria.
- Stores (inclusions): glycogen granules (carbohydrates) and lipid droplets (fats).
- Energy sources: ATP serves as the immediate source (hydrolyzed via myosin ATPase activity). During peak exertion and ATP depletion, creatine phosphate steps in, donating its phosphate group to instantly replenish ATP levels.