1/60
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai |
|---|
No study sessions yet.
Tissue
cooperative assembly of cells and extracellular matrix woven together to form a multicellular fabric with a distinctive function
what gives supportive tissues their strength
extracellular matrix
2 ways that cells adhere to each other to transmit physical stresses
extracellular matrix (ECM)
cytoskeleton and cell-cell adhesions that connect the cytoskeletons of neighbouring cells
which method of stress transmittingness do plants vs animals use
plants- ECM
animals- both in diff. tissue types
cell wall
supportive matrix in plants
can be hard (wood) or flexible (leaf)
newly formed vs cell growth stops cell walls
new= primary cell wall (flexible for additional growth)
old= secondary cell wall (hard for structure)
what gives a cell wall its tensile strength
cellulose microfibrils
cellulose
long unbranched chains of linked glucose subunits
how many cellulose molecules assemble to form a microfibril
16
primary vs secondary cell walls ingredients
primary= pectin
secondary= cellulose
matrix=
cellulose + pectin
pectin
long complex polysaccharides- rich in galacturonic acid
highly hydrated, binds cations
middle lamella function
cements cell walls together (is rich in pectin)
wood structure
cells thick walls remain when cell dies
form long channels vertically in tree
lignin in cell wall rigid when wet
cell wall structure
polysaccharides (CO2 and H2O)
some proteins
connective tissues vs epithelial tissues
connective have more ECM
collagen fibril organisation
Monomer- trimer- fibril- fibre
fibroblast secretes
collagen and other ECM
why are collagen fibrils arranged in layers in skin
allows skin to resist tensile stress in multiple directions
collagen fibril arrangement in tendon
tendons attach muscle to bone
collagen fibres align in parallel, along the axis of extension
integrins coordination of cell movements
new attachment points are established at the front of a moving cell
old adhesions are released at the back
enables the cell to crawl forwards
why are GAGs highly negatively charged
keeps high cation conc. in ECM
draws in water
creates swelling pressure
tissue specific ECM composition
dense connective tissue (bone, tendon)- less GAG + more collagen
vitreous humour- lots of GAG, little collagen
proteoglycan functions
binding growth factors
controlling migration of cells through the ECM
epithelium
sheets of cells joined together side by side
epithelia functions
cover external surfaces and line all internal cavities
create barriers
controls movement of molecules in and out
has receptors for external signals
protects against invading microbes and fluid loss
columnar epithelia
secretion/ absorption in the lining of the intestine
cuboidal epithelia
secretion/ absorption in the lining of the kidney tubules
squamous epithelia
filtration in the lining of the lungs
stratified epithelia
protection in the epidermis of the skin
basal lamina
thin, tough sheet of ECM (collagen, laminin)
seperates the epithelial cells from the network of collagen fibres in the underlying connective tissue
supports epithelial sheets
composition of basal lamina
ECM composed mainly of type IV collagen and laminin
where is the collagen and laminin supplied from (basal lamina structure)
colagen supplied by the underlying stromal cells (connective tissue)
laminin supplied by overlying epithelial cells
polarity of the epithelium
epithelial sheet has 2 faces
apical surface is free and exposed to the air or bodily fluids
basal surface is attached to a sheet of connective tissue called the basal lamina
why is polarity essential for epithelial cell function
the gut is lined by absorptive epithelial cells
also contains secretory goblet cells
polarity is critical for the function of both cell types
tight junctions
stitch cells together
adherens junctions
join actin filaments of neighbouring cells
desmosomes
join intermediate filaments of neighbouring cells
hemidesmosomes
join intermediate filaments to the basal lamina
gap junctions
form tunnels of aqueous connectivity between cells
Spina bifda
occurs when neural tube fails to close or form
abnormalities of the spinal chord
often leads to neurological deficits, typically affecting motor/ sensory function
Epidermolysis bullosa (EB)
genetic skin disorder resulting in blisters and lesions
gene therapy is used to correct defect in mutant gene (eg encoding laminin)
gap junction
small region of plasma membrane where two cells are very closely apposed in parallel
gap junction function
to allow small, intracellular, watersoluble molecules (eg metabolites) to move from cell to cell
gap junction physiology
molecular flow creates an electrical and a mechanical coupling between cells
gap junction permeability
gap junctions are gated
GJ permeability can be regulated by extracellular signals
gap junctions in retinal neurons
increased light triggers dopamine release, which switches retina from using rod (good in low light) to cone photorecetors (good in bright light)
plants and gap junctions
do not have gap junctions
plasmodesmata in cell walls carry out the function of gap junctions
different types of cadherins
E-cadherins
N-cadherins
P-cadherins
E-cadherins
mainly expressed on epithelial cells
N-cadherins
expressed on nerve, muscle and lens cells
P-cadherins
expressed in placenta and epidermis
cadherins mediate homophilic adhesion
provides a mechanism by which cells can recognise and stick to other similar cells
cadherin- cadherin interaction strength
weak but with multiple it is very strong
cadherin expression and affinity of cell-cell interaction
cells with higher cadherin levels form a stronger interaction, more tightly compacted in centre of assembly
selectins
cell surface proteins that bind carbohydrates
What causes leukocyte adhesion deficiency (LAD) disorders
molecular defects in selectin ligands, integrin expression or integrin activation on leukocytes
why must the ECM be degraded
to allow cells to pass between endothelial cells
ECM degrading enzymes
matrix metalloproteinases (MMPs)
Serine proteases
activity of ECM degrading proteases
some secreted in inactive form
some are confined to cell surface receptors
some are inhibited by the actions of locally secreted inhibitors