Lecture 16- Tissue organization Flashcards

1
Q

Cellular Tissues

A
  • Composed mostly of cells
  • Cell-cell and cell-ECM interactions (adherens junctions) in conjunction with interactions with the cytoskeleton within the cell provide the strength/integrity of the tissue
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2
Q

Connective Tissues

A
  • Composed primarily of ECM with a few cells
  • Cells synthesize and bind to the ECM that surrounds them
  • Physical properties of tissue are provided by organization of the ECM
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3
Q

Junctions of cellular tissues

A

1) Tight junction
2) Adherens junction
3) Desmosome junction
4) Gap junction
5) Hemidesmosome junction
6) Focal adhesions (Cell-ECM junction)

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4
Q

Adhering junctions (anchoring)

A

(Adherens, desmosomes, hemidesmosomes, focal adhesions)

Maintain the tissue when subjected to mechanical stress

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5
Q

Three basic units of adhering junctions

A

1) Transmembrane glycoprotein component–interacts either with proteins on adjacent cells or with proteins of the ECM
2) A complex of proteins on the cytoplasmic face of the junction forming a plaque–mediates the association between the membrane protein and the third component of the junction
3) Cytoskeleton network–may be actin filaments or intermediate filaments (without this the glycoproteins could just be pulled out of the membrane!!)

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6
Q

Adherens junctions

A
  • Cell-cell junction
  • Cadherins are the major transmembrane protein component (glycoprotein)
  • Associate with other Cadherins via homophilic interactions
  • Actin filaments around the perimeter
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7
Q

Role of Adherens in development

A
  • Positioning of adherens junctions toward the apical surface of cells allows for oriented contractions of the actin filaments to initiate an invagination of an epithelial sheet which can pinch off the form a tube
  • Formation of neural tube during embryogenesis
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8
Q

Focal adhesions

A
  • Cell-matrix anchoring junction
  • Integrins are the transmembrane glycoproteins (alpha, beta heterodimeric proteins)
  • Actin cytoskeleton
  • Heterophilic type junction
  • Interact with surrounding extracellular matrix
  • Important in cancer cell migration, metastasis, immune surveillance, and tissue repair
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9
Q

Desmosomes

A
  • Intermediate filament based adhering junction
  • Cell-cell anchoring junction
  • Cadherins are the gylcoprotein (homophilic interaction)
  • Plaque proteins interact with intermediate filament cytoskeleton
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10
Q

Hemi-desmosomes

A
  • Intermediate filament based adhering junction
  • Cell-matrix anchoring junction
  • Integrin a6B4 is the major glycoprotein
  • It’s the only integrin to associate with intermediate filaments
  • Link epithelial cells to the underlying basal lamina
  • Heterophilic interaction
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11
Q

Pemphigus

A

Autoimmune disease to skin desmosomal cadherin causing destabilization of cell-cell interactions

Can cause severe blistering

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12
Q

Epidermolysis bulosa simplex

A

Defect in intermediate filament assembly causing loss of integrity of desmosomes and hemidesmosomes

Can cause severe blistering

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13
Q

Tight junctions

A

Two functions:

  • Join neighbors to form permeability barrier across epithelial sheets
  • Maintain the cells polarity
  • Continuous strands of a transmembrane protein called claudin and occludin that interact with the same protein on the membrane of the adjacent cell (homophilic interaction)
  • Cytoskeleton not required for integrity of tight junctions
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14
Q

Gap Junctions

A

-Facilitate communication between neighboring cells
-Apparent in tissues comprised of electrically excitable cells
-Can help set up concentration gradients
-Protein component is connexins
-6 connexins make a connexon
-Junction is composed of many individual connexons associating
-Permeability regulated by pH and Ca levels
(high Ca, low pH= closed)

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15
Q

Connective tissues

A
  • Synthesized by a small number of cells
  • Strength provided by ECM
  • In many connective tissues cells called fibroblasts generate ECM
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16
Q

Three major structural components of ECM that contribute to the phenotype of connective tissues

A

-Fibrous proteins

-

17
Q

Fibrous proteins

A
  • Collagen I, II, III–fibrillar collagen

- Provides tensile strength–resists stretching

18
Q

Ehlers Danlos Syndrome

A
  • Failure to effectively assemble individual collagen molecules into fibrils
  • Hyperextensible skin
19
Q

Fibrillar collagen biosynthesis

A
  • Synthesized as a pro-alpha chain molecule in the ER
  • Post-translational modifications occur in Golgi, three pro-alpha chains associate into a triple helix (pro-collagen molecule)
  • SECRETED FROM CELL
  • Outside cell collagenases clip off pro-peptides allowing self-association into higher order structures forming fibrils and fibers
20
Q

Non-fibrillar collagen

A
  • Cannot form fibrils
  • Pro-peptide not cleaved
  • Forms a mesh and is major component of basal lamina
21
Q

Elastin

A
  • Allows stretching
  • Extensively cross-linked into fibers
  • Covalent interactions between lysine residues
  • Properties due to many random coils and prolines causing kinks in the chains
22
Q

Fibrillin

A

Limits the stretching of elastin fibers

-Marfans syndrome–mutation in fibrillin gene, lead to weak artery walls

23
Q

Bulky filler proteins/molecules

A
  • Cartilage and loose connective tissues
  • Resist compression forces
  • Permit rapid diffusion of soluble molecules
  • Permit cell migration
24
Q

Proteoglycans

A

Major component of loose connective tissue and cartilage

25
Q

Glycosaminoglycans (GAGs)

A

Chains of repeating disaccharides

26
Q

Core protein backbone (in proteoglycans)

A

Covalent link to GAGs via serine res

27
Q

Cross linker proteins

A

Fibronectin–multidomain glycoprotein, homodimer, can self associate into bundles and fibers, alternate splice variants , MULTIPLE DOMAINS MAKE IT A LINKER PROTEIN, TIES THINGS TOGETHER

Laminin–Three chain polypeptide, doesn’t bind to fibrillar collagens, component of basal lamina

28
Q

Basal lamina

A

Specialized ECM forming a dense meshwork
Links cellular tissues with connective tissues
Composed of: Type 4 collagen, Laminin, and proteoglycans