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CELL JUNCTIONS
PRESENTED BY:
DR.SHAIMAA
P.G ORAL PATHOLOGY
CYTOSKELETON
Cells possess a cytoskeleton that provides
a structural framework,
facilitates intracellular transport,
supports cell junctions and
transmits signals about cell contact and adhesion, and
permits motility.
Cell junctions ppt
MICROFILAMENTS: Maintenance of cell shape, movement, and
contractility. They are composed predominantly of a contractile
protein called actin, which is the most abundant cellular protein.
INTERMEDIATE FILAMENTS: Important in the maintenance
of cell shape and contact between adjacent cells and the
extracellular matrix
Microtubules: Provide internal support for the cell and are the basis of motility for
certain organelles, such as cilia; act as guide paths and part of the motor mechanism
for the movement of secretory vesicles and other organelles; and serve to position
certain organelles within the cell.
INTERCELLULAR JUNCTIONS
Cell junctions consist of multiprotein complexes that provide contact between neighbouring cells or between a cell and the
extracellular matrix. They also build up the paracellular barrier of epithelia and control the paracellular transport.
On the molecular level, intercellular junctions
typically consist of three components which
differ depending on the type of junction:
Transmembrane adhesive protein
Cytoplasmic adapter protein
Cytoskeletal filaments
Occluding junctions or tight junctions
The borders of two cells are fused together, often around the whole
perimeter of each cell, forming a continuous belt like junction known as a
tight junction or zonula occluden
Adhesive junctions or anchoring junctions:
In this type of junction cells anchor to the extracellular matrix. The intercellular
space is maintained at approx.20nm. They can appear as bands encircling the cell
(zonula adherens) or as spots of attachment to the extracellular matrix (adhesion
plaques).
Actin filaments attachments site
Zonula adherens and focal adhesions:
The principal transmembrane protein are members of the cadherin family. E-cadherin is a single-
pass, transmembrane glycoprotein that belongs to the classical cadherin family of Ca2+-
dependent adhesion proteins. Different members of the cadherin family are found in different
locations.
CDH1 - E-cadherin (epithelial): E-cadherins are found in epithelial tissue
CDH2 - N-cadherin (neural): N-cadherins are found in neurons
CDH12 - cadherin 12, type 2 (N-cadherin 2)
CDH3 - P-cadherin (placental): P-cadherins are found in the placenta
Intermediate filaments attachments sites
Desmosomes and hemidesmosomes:
Desmosomes are intercellular junctions of epithelia and cardiac muscle. They resist mechanical stress because they adopt a
strongly adhesive state in which they are said to be hyper-adhesive and which distinguishes them from other intercellular
junctions; desmosomes are specialised for strong adhesion and their failure can result in diseases of the skin and heart
Hemidesmosomes link the cell to the basal lamina and, through additional
extracellular molecules, to the rest of the extracellular matrix.
Significance: Several types of epidermolysis bullosa, a blistering skin disorder,
have been shown to be caused by mutations of the genes for various
desmosomal, hemidesmosomal, and intermediate filament proteins. In addition,
some forms of the disease are caused by mutations of the genes for
extracellular matrix proteins involved in cell-matrix adhesion. Pemphigus
vulgaris and pemphigus foliaceus, blistering diseases of the oral mucosa and
skin, respectively, are caused by autoantibodies to desmoglein-3 and
desmoglein-I, the cadherin in desmosomes.
Channel forming junctions
Gap junctions Gap junctions are plaque-like regions of the cell membrane where the intercellular space narrows
to 2 to 3 nm and transmembrane proteins of the connexin family form aqueous channels between the
cytoplasm of adjacent cells.
Signal relaying junctions
Chemical synapse:
Chemical synapses are specialized junctions through which neurons signal to each other and to non-neuronal cells such as those
in muscles or glands. Chemical synapses allow neurons to form circuits within the central nervous system.the key feature is the
presence of synaptic vesicles at presynaptic terminals. These vesicles are filled with 1 or more neurotransmitters. It is these
chemical agents that act as messengers between the communicating neurons that gives it a name as chemical synapse.
EPITHELIUM-CONNECTIVE TISSUE INTERFACE
All epithelia are separated from the underlying connective tissue by a layer of extracellular matrix organized as a thin sheet
immediately adjacent to the epithelial cells. The basal lamina, along with hemidesmosomes, attaches the epithelium to the
underlying connective tissue, functions as a filter to control the passage of molecules between the epithelium and
connective tissue, and acts as a barrier to cell migration.

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Cell junctions ppt

  • 2. CYTOSKELETON Cells possess a cytoskeleton that provides a structural framework, facilitates intracellular transport, supports cell junctions and transmits signals about cell contact and adhesion, and permits motility.
  • 4. MICROFILAMENTS: Maintenance of cell shape, movement, and contractility. They are composed predominantly of a contractile protein called actin, which is the most abundant cellular protein.
  • 5. INTERMEDIATE FILAMENTS: Important in the maintenance of cell shape and contact between adjacent cells and the extracellular matrix
  • 6. Microtubules: Provide internal support for the cell and are the basis of motility for certain organelles, such as cilia; act as guide paths and part of the motor mechanism for the movement of secretory vesicles and other organelles; and serve to position certain organelles within the cell.
  • 7. INTERCELLULAR JUNCTIONS Cell junctions consist of multiprotein complexes that provide contact between neighbouring cells or between a cell and the extracellular matrix. They also build up the paracellular barrier of epithelia and control the paracellular transport.
  • 8. On the molecular level, intercellular junctions typically consist of three components which differ depending on the type of junction: Transmembrane adhesive protein Cytoplasmic adapter protein Cytoskeletal filaments
  • 9. Occluding junctions or tight junctions The borders of two cells are fused together, often around the whole perimeter of each cell, forming a continuous belt like junction known as a tight junction or zonula occluden
  • 10. Adhesive junctions or anchoring junctions: In this type of junction cells anchor to the extracellular matrix. The intercellular space is maintained at approx.20nm. They can appear as bands encircling the cell (zonula adherens) or as spots of attachment to the extracellular matrix (adhesion plaques).
  • 11. Actin filaments attachments site Zonula adherens and focal adhesions: The principal transmembrane protein are members of the cadherin family. E-cadherin is a single- pass, transmembrane glycoprotein that belongs to the classical cadherin family of Ca2+- dependent adhesion proteins. Different members of the cadherin family are found in different locations. CDH1 - E-cadherin (epithelial): E-cadherins are found in epithelial tissue CDH2 - N-cadherin (neural): N-cadherins are found in neurons CDH12 - cadherin 12, type 2 (N-cadherin 2) CDH3 - P-cadherin (placental): P-cadherins are found in the placenta
  • 12. Intermediate filaments attachments sites Desmosomes and hemidesmosomes: Desmosomes are intercellular junctions of epithelia and cardiac muscle. They resist mechanical stress because they adopt a strongly adhesive state in which they are said to be hyper-adhesive and which distinguishes them from other intercellular junctions; desmosomes are specialised for strong adhesion and their failure can result in diseases of the skin and heart
  • 13. Hemidesmosomes link the cell to the basal lamina and, through additional extracellular molecules, to the rest of the extracellular matrix. Significance: Several types of epidermolysis bullosa, a blistering skin disorder, have been shown to be caused by mutations of the genes for various desmosomal, hemidesmosomal, and intermediate filament proteins. In addition, some forms of the disease are caused by mutations of the genes for extracellular matrix proteins involved in cell-matrix adhesion. Pemphigus vulgaris and pemphigus foliaceus, blistering diseases of the oral mucosa and skin, respectively, are caused by autoantibodies to desmoglein-3 and desmoglein-I, the cadherin in desmosomes.
  • 14. Channel forming junctions Gap junctions Gap junctions are plaque-like regions of the cell membrane where the intercellular space narrows to 2 to 3 nm and transmembrane proteins of the connexin family form aqueous channels between the cytoplasm of adjacent cells.
  • 15. Signal relaying junctions Chemical synapse: Chemical synapses are specialized junctions through which neurons signal to each other and to non-neuronal cells such as those in muscles or glands. Chemical synapses allow neurons to form circuits within the central nervous system.the key feature is the presence of synaptic vesicles at presynaptic terminals. These vesicles are filled with 1 or more neurotransmitters. It is these chemical agents that act as messengers between the communicating neurons that gives it a name as chemical synapse.
  • 16. EPITHELIUM-CONNECTIVE TISSUE INTERFACE All epithelia are separated from the underlying connective tissue by a layer of extracellular matrix organized as a thin sheet immediately adjacent to the epithelial cells. The basal lamina, along with hemidesmosomes, attaches the epithelium to the underlying connective tissue, functions as a filter to control the passage of molecules between the epithelium and connective tissue, and acts as a barrier to cell migration.