Sliding filament model of muscle contraction

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Sliding filament model of muscle contraction

MSK Module Content

MSK Module Content

Resting membrane potential
Action potentials in myocytes
Neuron action potential
Neuromuscular junction and motor unit
Sliding filament model of muscle contraction
Cholinergic receptors
Lambert-Eaton myasthenic syndrome
Neuromuscular junction disorders: Pathology review
Myasthenia gravis
Myalgias and myositis: Pathology review
Pediatric orthopedic conditions: Clinical
Muscle weakness: Clinical
Slow twitch and fast twitch muscle fibers
Muscle spindles and golgi tendon organs
Muscle contraction
Skeletal muscle histology
Muscular system anatomy and physiology
Lower back pain: Clinical
Back pain: Pathology review
Systemic lupus erythematosus (SLE): Clinical
Osteoporosis
Child abuse: Clinical
Non-steroidal anti-inflammatory drugs
Rheumatoid arthritis
Physiological changes during exercise
Polymyositis
Lordosis, kyphosis, and scoliosis
Spinal disc herniation
Acetaminophen (Paracetamol)
Osteochondroma
Scleroderma
Skeletal system anatomy and physiology
Bone remodeling and repair
Legg-Calve-Perthes disease
Genu varum
Inflammatory myopathies: Clinical
Muscular dystrophies and mitochondrial myopathies: Pathology review
Mitochondrial myopathy
Inclusion body myopathy
Monoclonal antibodies
Spondylolysis
Spondylosis
Spondylitis
Bone disorders: Pathology review
Muscular dystrophy
Mixed connective tissue disease
Cartilage histology
Raynaud phenomenon
Scleroderma: Pathology review
Osteoarthritis
Cartilage structure and growth
Fibrous, cartilage, and synovial joints
Septic arthritis
Slipped capital femoral epiphysis
Bone tumors
Osgood-Schlatter disease (traction apophysitis)
Achondroplasia
Rheumatoid arthritis: Clinical
Developmental dysplasia of the hip
Bone tumors: Pathology review
Neck trauma: Clinical
Spinal cord reflexes
Pediatric bone and joint infections: Clinical
Paget disease of bone
Bone histology
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Anatomy clinical correlates: Bones, joints and muscles of the back
Joints of the wrist and hand
Osteomalacia and rickets
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Brachial plexus
Anatomy of the brachial plexus
Klumpke paralysis
Anatomy clinical correlates: Wrist and hand
Muscles of the hand
Achilles tendon rupture
Rotator cuff tear
Somatosensory receptors
Carpal tunnel syndrome
Patellar tendon rupture
Ankylosing spondylitis
Marfan syndrome
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Reactive arthritis
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Ehlers-Danlos syndrome
Alport syndrome
Gout
Gout and pseudogout: Pathology review
Antigout medications
Nucleotide metabolism
Joint pain: Clinical
Lesch-Nyhan syndrome
Thoracic outlet syndrome
Introduction to the muscular system
Introduction to the skeletal system
Development of the muscular system
Torticollis
Pigeon toe
Neuromuscular blockers
Myotonic dystrophy
Development of the axial skeleton
Development of the limbs
Muscles of the back
Anatomy of the arm
Anatomy clinical correlates: Clavicle and shoulder

Transcript

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In order for a skeletal muscle to contract, your brain sends a signal, from an upper motor neuron down the spinal cord where it synapses with the cell bodies of lower motor neurons located in the anterior horn of the spinal cord.

From here, the signal travels through the lower motor neuron’s axon and until it reaches the axon terminal which is next to a muscle fiber.

At the site where an axon terminal meets the muscle fiber, called the neuromuscular junction, it releases small membrane-enclosed synaptic vesicles filled with acetylcholine.

Acetylcholine is a neurotransmitter that tells the muscle to contract.

Now before we continue with the actual events that happen during the contraction, let’s focus on one muscle cell a myocyte and its functional units called sarcomeres.

A myocyte is a long cylindrical cell with multiple nuclei located just below the sarcolemma, which is the cell membrane.

The sarcolemma is unique because it makes these tiny tunnels called T-tubules that project downwards from the surface towards the center of the muscle fiber.

The cytoplasm of a myocyte is called sarcoplasm, and the myocyte has a special type of smooth endoplasmic reticulum which is called sarcoplasmic reticulum.

The sarcoplasmic reticulum stores lots of calcium and runs parallel to the T tubules.

Now, the sarcoplasm is filled with stacks of long filaments called myofibrils and each myofibril consists of contractile proteins and regulatory proteins.

Contractile proteins include thick myosin and thin actin filaments.

The thick myosin filament is made up of hundreds of myosin proteins, and each myosin protein has a tail and two myosin heads - it looks a bit like two golf clubs with their handles twisted around one another.

Multiple myosin proteins join their tails together to form the central part of the thick filament.

In comparison, the thin actin filaments are made up of small, globular proteins called G-actin.

Each G-actin has an active site where the myosin head binds to it during contraction.

These G-actin proteins forms a filament that looks like a long helix structure -- like a pearl necklace that’s gently twisted. This entire filament is called F-actin.

F-actin is associated with two regulatory proteins - tropomyosin and troponin.

Tropomyosin is a string-like protein that wraps around F-actin, covering its active sites so that the myosin heads can’t bind to it.

Troponin proteins are smaller and are made up of three subunits - there’s a T subunit that binds to tropomyosin, an I subunit that binds to F-actin, and a C subunit that binds to calcium ions.

Together, the F-actin, the troponin and tropomyosin make a complete thin filament.

As it turns out, these thick and thin filaments don’t extend through the entire length of the myocyte, but instead, they’re arranged in short units called sarcomeres.

When we look at sarcomeres with an electron microscope, the thick myosin filaments look dark, while the thin actin filaments look light which gives the muscle fiber a striped appearance.

Alright, now let’s zoom in and relate these bands to a structure of one sarcomere. At the center of the sarcomere is the M line made of myomesin proteins, where the thick filaments attach.

At the borders of the sarcomere are the two Z-discs made of alpha actin proteins, where the thin filaments attach.

For every thick filament, there are two thin filaments-one above and one below and the two types of filaments overlap.

Key Takeaways

The sliding filament model of muscle contraction describes how muscles generate force and produce movement. Muscle contraction occurs as a result of the sliding of thin filaments (actin) over thick filaments (myosin) within muscle fibers.

The process of contraction starts when an action potential reaches the muscle fiber and triggers the release of calcium ions from the sarcoplasmic reticulum. The calcium ions bind to the protein troponin, which in turn causes a conformational change in tropomyosin, exposing the myosin binding sites on the actin filaments. Myosin heads then bind to the actin filaments and generate force. Attachment and detachment between actin and myosin occur several times during a single contraction.

Sources

  1. "Medical Physiology" Elsevier (2016)
  2. "Physiology" Elsevier (2017)
  3. "Human Anatomy & Physiology" Pearson (2017)
  4. "Principles of Anatomy and Physiology" Wiley (2014)
  5. "Fifty years of muscle and the sliding filament hypothesis" European Journal of Biochemistry (2004)
  6. "Structural Basis of the Cross-Striations in Muscle" Nature (1953)
  7. "Mechanism of Muscular Contraction" (2014)