BMS11004 - WEEK 3 WEDNESDAY Flashcards
synapses, gap junctions, electrical and chemical synapses, neuromuscular junctions, varieties of CNS synapses
how can synapses enable flexible processing
increase complexity, and flexibility for integration (interneurons can allow multiple inputs)
what is strcture of electrical synapse
gap junctions (direct pore) allowing current to directly pass between neuron without chemicals, making cytoplasms of 2 neuron continuous
how large is gap junction diameter
1-2nm
how can you tell if 2 neurons are connected by gap junctions (electrical synapse)
- dye injection- small molecule so can diffuse across gap
- if can transmit both hyperpolarisations and depolarisations then is a electrical synapse
if delete a connexin gene then stops as gene is required when building gap junctions
what are electrical synapses used for
reflex actions = fast communication and synchronising neurons, if necessary
provide overview in chemical synaptic transmissions
- package NT into vesicle, move to pre-synaptic terminal
- AP arrive, open v/gated Ca2+ channels
- Ca2+ influx cause vesicles fuse to membrane and release NT
- NT diffuse across synaptic cleft, activates receptor on PSC, further signalling
- NT removed from cleft
name the 2 major vesicle catagory types
defined by what is inside
- synaptic vesicles, dense-core secretory granules
compare structures of synaptic vesicles and dense-core secretory granules
SV = clear and small (40-50nm)
DCSG = dense and large (100nm)
compare what synaptic vesicles and dense-core secretory granules carry
SV = small molecule transmitters (eg: glutamate)
DCSG = peptide NT eg: amino acids, opioidsm endorphins
explain how synapic vesicle and dense-core secretory-granules are filled
SV = filled by presynaptic terminal transporter protein
DCSG = created and filled by ER/Golgi apparatus
compare lifespans for synaptic vesicles and dense-core secretory granules
SV = recycled via endocytosis
DGSG = one+done
how can you record how Ca2+ channels open
use calcium sensitive flurorescent proteins
explain how vesicles bind to membrane, using SNARE proteins (including v-SNARE, t-SNARE, synaptotagmin and “zipper”)
v-SNARE = vesicle
t-SNARE = target
when Ca bind to synaptotagmin, conformational change make SNAREs ‘zipper’ together and force vesicle to fuse to membrane
what are SNARE-proteins used for
targets for toxins like botulinum and tetnus
used to transport proteins around cells using their ‘zippers’
state 2 different ways how NT can bind to postsynaptic receptor to initiate a process
- ligand-gated ion channel
- G-protein coupled receptor
explain how NT binding to postsynaptic receptors using ligand-gated ion channels (ionotropic receptor), impacts cell
directly depolarises/hyperpolarises postsynaptic cell
explain how NT binding to postsynaptic receptors using G-protein-coupled receptor (metabotropic receptors), impacts cell
causes biochem cascades, often involving enzymes
what is a GPCR
G-protein-coupled-receptors
G proteins which are coupled to other G protein that could be responsible for multiple different effects
name 3 methods of NT removal
1.diffuse away- takes time, not best way, and not temporally precise
2.actively taken up by transporters for recycling into presynaptic neuron/glia
3. destroyed in synaptic cleft by enzyme
give properties of electrical synapses (directions, speed)
signal pass in both direction
passed directly and can only be attenuated (make bigger or smaller but not inverted or changed direction)
fast (<0.3ms)
give properties of chemical synapses (directions, speed, signal transormations, modifablities)
signals pass in 1 direction but can be transformed to change direction, inverted, amplify
more ‘plastic’ = modifiable
slower (0.3-5ms)
what NT do neuromuscular junctions use?
acetylcholine
what are useful components of neuromuscular junctions (why may you want to use them)
fast and reliable, largest synapse in body, many active zones in pre-synap, junctional folds on post-syn precisely aligned to active zones = allow Ach to land exactly and definitely trigger contractions
explain how signals in neuromuscular junctions are released in discrete amount (not in continuous amounts)
statistical distribution of post-synaptic potential amplitudes shows NT in “quantum packets” with 1 quantum = 1 vesicle, filled with NT
cannot release half-vesicle, but release different number of whole vesicle
name different joinings for synapse
- axosomatic = soma
- axodendritic = dendrites
- axoaxonic = one terminal button onto another
- axospinous = presynaptic neurons onto post-dendritic spine
- dendrodentric = dendrites form synapse with others
- dendrosomatic = dendrite onto somas
explain how botulinum toxin causes paralysis
targets SNARE proteins, ‘zippers’ for movement of NT
so cannot move chemicals into vesicle for synaptic transmissions