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Cell adhesion
The process by which cells attach to each other or to the extracellular matrix (ECM) to maintain tissue structure and communication.
Cell adhesion molecules (CAMs)
Transmembrane proteins that mediate cell–cell and cell–matrix interactions.
Main CAM families
Cadherins, Selectins, Ig-superfamily CAMs, and Integrins.
Cadherins
Ca²⁺-dependent proteins responsible for strong cell–cell adhesion in tissues like epithelium and muscle.
E-cadherin
Found in epithelial tissues; loss of E-cadherin is linked to cancer metastasis.
P-cadherin
Present in placenta and epidermis.
N-cadherin
Found in neural tissue; plays a role in brain and nerve cell connections.
Protocadherins
Non-classical cadherins found mainly in the brain, important for neural diversity.
Desmosomal cadherins
Include desmoglein and desmocollin; provide mechanical strength to tissues like skin and heart.
T-cadherin
Attached to the membrane via lipids; found in muscles and nerves.
Cadherin function
Maintains adherens junctions and desmosomes, regulates development, cell polarity, and tissue morphogenesis.
Selectins
Ca²⁺-dependent transmembrane proteins that bind specific carbohydrates to mediate transient cell–cell adhesion in the bloodstream.
L-selectin
Found on leukocytes; helps them roll along vessel walls.
P-selectin
Found on platelets and activated endothelial cells.
E-selectin
Found on activated endothelial cells; promotes leukocyte adhesion during inflammation.
Leukocyte extravasation
The process by which leukocytes roll, adhere, and migrate out of blood vessels into tissues.
Ig-superfamily CAMs (Ig-CAMs)
Ca²⁺-independent adhesion molecules containing immunoglobulin-like domains; involved in immune and neural cell adhesion.
ICAM-1 and VCAM-1
Found on endothelial cells; mediate leukocyte binding during inflammation.
NCAM
Found on nerve cells; promotes adhesion during neural development and regeneration.
L1-CAM
Mutations cause L1 syndrome (neurological disorder with mental retardation and hydrocephalus).
Integrins
Transmembrane heterodimers (α and β subunits) that mediate cell–ECM adhesion and signal transduction.
Integrin ligands
Fibronectin, collagen, laminin, and vitronectin.
Integrin functions
Mediate adhesion, transmit signals, convert mechanical forces to biochemical signals, and help immune cells migrate.
Occluding junctions
Tight junctions that seal neighboring cells to prevent leakage of molecules.
Anchoring junctions
Junctions that mechanically attach cells to one another or to the ECM.
Communicating junctions
Junctions that allow the passage of ions and small molecules between cells (e.g., gap junctions).
Tight junctions
Form a barrier at the apical side of epithelial cells; composed of claudins and occludins.
Adherens junctions
Cadherin-based junctions linked to actin filaments; form adhesion belts below tight junctions.
Desmosomes
Button-like junctions connecting intermediate filaments between cells; provide mechanical strength.
Focal adhesions
Integrin-based junctions connecting actin filaments to the extracellular matrix.
Hemidesmosomes
Integrin-based junctions that anchor epithelial cells to the basal lamina via intermediate filaments.
Gap junctions
Channels formed by connexons (6 connexins) that allow ions and small molecules to pass between cells.
Connexins
Channel-forming proteins that create connexons in gap junctions.
Gap junction function
Enable direct electrical and metabolic communication between adjacent cells.
Regulation of gap junctions
Can open or close in response to changes in pH, Ca²⁺ levels, or extracellular signals.
Importance of cell adhesion
Essential for embryonic development, immune responses, wound healing, and tissue repair.
Disease link: Cancer
Loss of E-cadherin or abnormal integrin signaling leads to metastasis.
Disease link: Autoimmune disorders
Overexpression of ICAM/VCAM causes chronic inflammation.
Disease link: Neurological disorders
L1-CAM mutations cause developmental brain defects.
Mechanotransduction
The process by which integrins convert mechanical forces from the ECM into biochemical signals.