Heart Physiology Vid 1 Part 2

Cellular junctions overview

  • Gap junctions

    • Transmembrane proteins that span the plasma membranes of two adjacent cells.

    • Comprised of subunits that form tiny tunnels/passageways, allowing solutes to pass from one cell to the next.

  • Tight junctions

    • Transmembrane proteins between the plasma membranes of two cells.

    • Function: seal the space between cells to keep certain substances like liquids confined to a lumen or cavity (compartmentalization).

    • Examples: within blood vessels to keep blood components inside the vessel walls; in the urinary bladder to prevent urine from seeping between epithelial cells until urination.

  • Adherens junctions

    • Found in epithelial tissues with microvilli.

    • Provide structural integrity and resist pulling forces, preventing cells from pulling apart under stress.

  • Desmosomes

    • Comprised of a thick protein plaque linked to keratin (intermediate filaments) via cadherin proteins.

    • Button-like junctions that keep cells together in tissues subjected to stretching and twisting to maintain tissue integrity.

  • Hemidesmosomes

    • Not cell-to-cell junctions.

    • Anchor the basal surface of epithelial cells to the basement membrane.

    • Distinguish from other junctions by connecting cells to the extracellular matrix rather than to neighboring cells.

Cardiac muscle tissue: linking junctions to function

  • Cardiac muscle fibers are also called cardiomyocytes; they are striated and contract via the sliding filament mechanism.

  • Sarcomere: the basic contractile unit, defined from one Z disc to the next Z disc (Z disc = Z line).

    • Thin filaments: actin, tropomyosin, troponin, nebulin.

    • Thick filaments: myosin.

      Shape and size Differences

    • Skeletal muscle fibers: long and cylindrical; multinucleated.

    • Cardiomyocytes (cardiac muscle fibers): short, branched, usually uninucleated with a single central nucleus; extensive capillary supply.

  • Metabolic apparatus

    • Cardiomyocytes contain many mitochondria (about 25%25\% of the cell volume) to support continuous aerobic respiration for ATP production.

    • This high mitochondrial content reflects the heart’s constant demand for oxygen.

  • Blood supply

    • The heart has an extensive capillary network to sustain continuous function.

  • Ultrastructural differences in calcium handling

    • Cardiomyocytes: T-tubules are wider and fewer in number.

    • Sarcoplasmic reticulum (SR) is simpler and lacks large terminal cisternae.

    • No triads in cardiomyocytes; instead, the dyadic arrangement (T-tubule with a nearby SR segment) is present, and not a classic triad as in skeletal muscle.

  • No triads in cardiomyocytes

    • In skeletal muscle, the triad consists of a transverse tubule flanked by terminal cisternae on both sides: extTriad=(extterminalcisterna)extTtubule(extterminalcisterna)ext{Triad} = ( ext{terminal cisterna}) - ext{T-tubule} - ( ext{terminal cisterna})

    • In cardiomyocytes, the SR does not form large terminal cisternae around T-tubules, so classic triads are not present.

Intercalated discs and cell-to-cell coupling in the heart

  • Intercalated discs

    • Unique to cardiac muscle; interdigitating folds of the sarcolemma increase surface area for cell-to-cell contact.

    • Help neighboring cardiomyocytes interlock and communicate more effectively.

  • Junctions within intercalated discs

    • Desmosomes: provide strong mechanical linkage to keep cells bound during contraction and mechanical stress.

    • Gap junctions: allow ions and small solutes to pass directly between cells, promoting electrical coupling and synchronized contraction (the heart acts as a functional syncytium).

    • Fascia adherens (a type of adherens junction variant in cardiac tissue)

    • Actin filaments anchor to fascia adherens to reinforce cell–cell adhesion.

    • Fascia adherens contribute to the secure interaction of cardiomyocytes within the myocardium (the middle layer of the heart wall).

Terminology recap and functional significance

  • Sarcolemma: plasma membrane of a muscle fiber.

  • Sarcoplasm: cytoplasm of a muscle fiber.

  • Sarcoplasmic reticulum (SR): stores Ca²⁺ for muscle contraction; in skeletal muscle, terminal cisternae are prominent around T-tubules, forming a classic triad.

  • Transverse tubules (T-tubules): invaginations of the sarcolemma that penetrate into the sarcoplasm to quickly propagate action potentials.

  • Terminal cisternae: large SR storage sacs adjacent to T-tubules in skeletal muscle; form the triad.

  • Triad: specialized arrangement in skeletal muscle consisting of a T-tubule flanked by terminal cisternae on both sides; not present as such in cardiomyocytes.

  • Z disc (Z line): boundary between adjacent sarcomeres; defines the start and end of a sarcomere.

  • M line: center line in the sarcomere that holds thick filaments together.

  • Titin: elastic protein that anchors to the Z disc and helps center-and-stabilize the thick filaments during contraction.

  • Nebulin: helps stabilize the thin filament length.

  • Actin, tropomyosin, troponin: components of thin filaments that regulate contraction.

  • Myosin: major component of thick filaments that drives contraction via cross-bridge cycling.

Summary of key contrasts to study for exam readiness

  • Cardiac muscle features

    • Short, branched cardiomyocytes with single nucleus and extensive capillary network.

    • High mitochondrial content (~ 25%25\% of cell volume) for constant ATP production via aerobic respiration.

    • Intercalated discs containing desmosomes, gap junctions, and fascia adherens for mechanical and electrical coupling.

    • No classic triads; T-tubules are wider and fewer; SR is simpler.

  • Skeletal muscle features (for comparison)

    • Long, cylindrical, multinucleated fibers with well-developed triads (T-tubule + two terminal cisternae).

    • Distinct terminal cisternae arrangement around T-tubules in the SR.

  • Shared features

    • Both have sarcomeres from Z disc to Z disc, contain actin and myosin in thin and thick filaments, and rely on the sliding filament mechanism for contraction.

  • Practical implications

    • Intercalated discs enable rapid electrical coupling through gap junctions, essential for synchronized cardiac contraction.

    • Fascia adherens and desmosomes help cardiac tissue withstand mechanical stress during repeated cycles of contraction and relaxation.

    • The heart’s metabolism is tightly coupled to oxygen supply due to the high mitochondria content, underscoring the importance of coronary circulation.