Smooth muscle tissue
- Consists of bundles of elongated fusiform cells that lack striations
- Each fusiform cell has a single, centrally located nucleus
- Origin – mesenchyme
- Non-striated
- Slow, involuntary contraction
- ANS innervation
- Located in the walls of the hollow and tubular organs:
- Blood vessels
- Alimentary canal – function in peristalsis
- Respiratory tract
- Urogenital tract
- Associated with hair follicles in the skin
- Smooth muscles can undergo muscle hypertrophy
- Good regeneration capacity, involving mitotic activity of muscle cells
- No sarcomeres, but they do have myosin
- Smooth muscle fibres (leiomyocyte) are characterised by a fusiform shape
- The non-striated cells contain more actin than myosin in the fibre composition. Therefore, there is a larger proportion of thin filaments than thick filaments in smooth muscles than striated muscles
- The actin and myosin are arranged in a diagonal web-like structure around the cell and are attached to the cell membrane
- The contractile fibres are in less organised bundles rather than the sarcomeres observed in skeletal muscles. The resulting contraction moves the cell in various directions
- Smooth muscle is often layered in many different directions
There are two types of smooth muscle:
- Visceral smooth muscles:
- Small blood vessels, walls of hollow organs
- Poor nerve supply
- Abundant gap junctions
- Multi-unit smooth muscles:
- Large arteries, upper respiratory tract, muscles of hair follicles, iris and ciliary body of eye
- Rich nerve supply
- Allow for fine control
- Provide for very precise and graded contractions
Smooth muscle contraction:
- Smooth muscle cells have contractile apparatus of thin and thick filaments
- The thin and thick filament bundles form a lattice-network attached to the cell membrane
- The mechanism of contraction is different from striated muscles because smooth muscles lack troponin
- The activation of myosin is triggered by a calcium-binding protein called calmodulin
- When calcium ions are released from the extracellular fluid, they bind to the protein calmodulin. This activates an enzyme which phosphorylates the regulatory light chain myosin-heads. This activates myosin ATPase activity enabling cross-bridge formation and consequently muscular contraction