the extracellular space
DESCRIPTION
The Extracellular Space. Epithelial tissues closely packed cells lining spaces in the body (e.g. skin, intestine, etc) Connective tissues Largely composed of non-living extracellular material (e.g. cartilage, tendon, dermis). The Extracellular Matrix (ECM). - PowerPoint PPT PresentationTRANSCRIPT
The Extracellular Space• Epithelial tissues
– closely packed cells lining spaces in the body (e.g. skin, intestine, etc)• Connective tissues
– Largely composed of non-living extracellular material (e.g. cartilage, tendon, dermis)
The Extracellular Matrix (ECM)• An organized network of materials located beyond the plasma membrane
Basement membranes• Thick regions of ECM
– Surround muscle/fat– Underlie the basal surface of epithelial tissues
Basement membranes• Separate different tissues• Provide mechanical support• Barrier to macromolecule and cellular movement• Substrate for cell migration• Generate signals that maintain cell survival
ECM: Collagens• 27 different types
– High tensile strength (resistant to pulling forces)– Alpha-helical trimers bundle together into fibrils– Types I, II, III (fibrillar) form rigid cables
• Adjacent collagens are strengthened by covalent cross-links– Hydroxylysine - lysine
– Type IV (nonfibrillar) can form an interconnected lattice
ECM: Collagens• 27 different types
– Type IV (nonfibrillar) can form an interconnected lattice• Composed of helical and non-helical segments (flexibility)• Globular domains at each end (lattice contact points)
– Collagens bind:• Fibronectins• Integrins (cell surface)
ECM and disease• Diseases caused by defects in collagen genes
– Osteogenesis imperfecta• Fragile bones
– Ehlers-Danlos syndrome• Hyperflexible joints,
highly extensible skin
ECM: Proteoglycans• Protein core + glycosaminoglycan (GAG) polysaccharide complex
– High amount of negative charge binds cations and H2O– Hydrated gel resists compressive forces
• Hyaluronic acid links many proteoglycans to form large molecules• Fill the scaffold created by collagens
ECM: Fibronectins• Modular domains for interactions• Bind collagens, proteoglycans, integrins at cell surface
NC cells
ECM: Laminins• 3 polypeptides linked by disulfide bonds• Form a second lattice interwoven with
Collagen IV lattice• Bind to proteoglycans, integrins at cell
surface
PGC on laminin
ECM Remodeling• Matrix metalloproteinases (MMPs)
– Degrade ECM proteins to enable:• Tissue remodeling• Cell migration• Wound healing
Steps leading to metastatic spread
MMP activity
Cell - ECM Interactions
• Integrins– Only found in animals– Heterodimer of alpha and beta subunits
• 18 alpha and 8 beta subunits known• 12 different alpha/beta combinations known
– Transmembrane proteins• Extracellular domain, transmembrane domain, intracellular domain• Inside-out signaling
– Post-translational alterations to cytoplasmic tail regulate conformation changes in extracellular domain
– Talin separates beta from alpha to open receptor to active state
Plasma membrane
talin
Inactive
Active
Cell – ECM: Integrins• Ligand binding
– RGD loop of Fibronectin binds to integrin receptor extracellular domain
– Isolated RGD Loop can be exploited to block platelet aggregation / blood clotting
Cell – ECM: Integrins• Adhesion to substrate
– Receptors cluster increasing overall strength
• Signal transmission – Binding of ligand
(collagen) can change cytoplasmic domain
– Cytoplasmic domain can activate kinases such as FAK and Src
– Activated kinases can transmit signals to nucleus and change gene expression
Cell – ECM: Integrins• Structures important for adhesion to substrate
– Focal adhesions:• Scattered, discrete, transient, dynamic, rapidly form and break• Clusters of integrins bound to collagen / Fibronectin• Cytoplasmic domains attach to cytoskeleton connecting exterior forces to
internal signals– Actin filaments– Focal adhesion kinase (FAK)
Forces exerted by focal adhesions
Cell – ECM: Integrins• Structures important for adhesion to substrate
– Hemidesmosome• more permanent anchor to basement membrane• Integrins bound to laminin to dense collection of intermediate filaments
ECM and disease
(keratins)
• Disease: epidermolysis bullosa– Epidermis poorly connected to basement membrane / dermis– Fluid accumulates in between = blister
Epidermolysis Bullosa Type Genes Mutated
Simplex Keratin-5; Keratin-14; plectinJunctional laminin-5; collagen XVII; a6b4 integrinDystrophic collagen VII
Cell - ECM Interactions
Cell - Cell Interactions• Cadherins: Ca2+ dependent
adhesion– Homophilic interactions
allow self-sorting of mixed cell populations
– Disease role: metastasis of cancer• Lose adhesion by
downregulating cadherin expression
• Penetrate / invade barriers by upregulating MMP expression
Cell - Cell Interactions• Structures important for
cell-cell adhesion– Adherens junctions
(30nm gap between cells)• Cadherin-cadherin
interactions in belt-like strips holding two cells together
• Cytoplasmic domains link to the cytoskeleton
Cell - Cell Interactions• Structures important for cell-cell adhesion
– Desmosomes (1 um diameter disc)• Resist mechanical stress• Cadherin-cadherin interactions linked to cytoskeleton (intermediate
filaments)
Cell - Cell Interactions• Tight junctions
– Seal two membranes together– Block paracellular movement – Occludin and claudins (24 genes)– Important for maintaining blood-
brain barrier
Cell - Cell Interactions• Gap junctions
– Join cytoplasmic spaces between adjacent cells via a narrow pore• 1.5nm diameter• 1kD cutoff, small molecules freely pass (ATP, cAMP, Ca2+, etc)
– Subunits are connexins– Open / close regulated by phosphorylation– Integrates cells of a tissue into a functional unit
Cell - Cell Interactions
Plant cell-cell interactions• Plasmodesmata
– Join adjacent plant cytoplasmic spaces– Capable of dilation, 1kD cutoff can open to a 50kD cutoff– Exploited by some plant viruses
Roles of the plant cell wall• Structural role supporting and protecting plant cells
– Cellulose microfibrils confer tensile strength• Signaling roles
– Cell wall-associated transmembrane protein kinases • Dynamic not static, undergoes significant remodeling