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![Proteins associated with synaptic vesicles
(identified through sequencing and cloning of cDNA’s)
Membrane proteins
A.
B.
C.
Synaptophysin (~ 36 kD)
Synaptotagmin (~ 61 kD; the Ca2+ sensor)
Snares (residents of either the vesicle
[v-snare] or the target membrane [t-snare])
1.
VAMP (also called synaptobrevin), a v-snare (~18 kD)
2.
Syntaxin, a t-snare that also associates with Ca 2+
channels (~32 kD; technically not a vesicle protein)
3.
SNAP-25, a t-snare (~25 kD; also technically not a
vesicle protein)
D. Electrogenic proton ATPase -creates emf that drives
neurotransmitter uptake against a concentration gradient](https://image.slidesharecdn.com/neuromusculartransmission2008final-140219024809-phpapp02/75/Neuromuscular-transmission-21-2048.jpg)
![Proteins associated with synaptic vesicles
(identified through sequencing and cloning of cDNA’s)
Membrane proteins
A.
B.
C.
Synaptophysin (~ 36 kD)
Synaptotagmin (~ 61 kD; the Ca2+ sensor)
Snares (residents of either the vesicle
[v-snare] or the target membrane [t-snare])
1.
VAMP (also called synaptobrevin), a v-snare (~18 kD)
2.
Syntaxin, a t-snare that also associates with Ca 2+
channels (~32 kD; technically not a vesicle protein)
3.
SNAP-25, a t-snare (~25 kD; also technically not a
vesicle protein)
D. Electrogenic proton ATPase -creates emf that drives
neurotransmitter uptake against a concentration gradient](https://image.slidesharecdn.com/neuromusculartransmission2008final-140219024809-phpapp02/75/Neuromuscular-transmission-22-2048.jpg)
![Normal EPPs invariably evoke muscle action
potentials
• Normally, the average EPP amplitude = 60 mV
-In frog, ~150 vesicles
• Safety factor for transmission is therefore high (greater than 1)
- Frog example:
∆VEPP ÷ ∆VAPthreshold
= 60 mV ÷ │-90 mV*- [-50 mV] │
= 60 mV ÷ 40 mV = 1.5
(*muscle resting VM = -90 mV)](https://image.slidesharecdn.com/neuromusculartransmission2008final-140219024809-phpapp02/75/Neuromuscular-transmission-46-2048.jpg)
Uploaded byRahul Kumar
Neuromuscular transmission
The document discusses the anatomical and physiological aspects of synaptic transmission at the neuromuscular junction, detailing mechanisms such as neurotransmitter release, vesicle fusion, and termination processes. It highlights key proteins involved in vesicle dynamics and synaptic signaling, including various snares, receptors, and enzymes like acetylcholinesterase. Additionally, the concept of safety factors in neuromuscular transmission and the implications of channelopathies related to neurotransmitter receptors are presented.
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Anatomy is critical for synaptic function.
Discussion on NMJ structure, synaptic selectivity, and visual evidence from a frog's NMJ.
Discussion on NMJ structure, synaptic selectivity, and visual evidence from a frog's NMJ.
Discussion on NMJ structure, synaptic selectivity, and visual evidence from a frog's NMJ.
Overview of synaptic transmission steps including precursor transport, synthesis, storage, and quantum release.
Identification of synaptic vesicle proteins and the vesicle life cycle including vesicle fusion.
Details about synapse structure, exocytosis, and Ca2+ role in neurotransmitter release.
Measurement of mini and evoked amplitudes, cholinergic synapse structure, and action potential relationship.
Rapid inactivation of neurotransmitters by cholinesterase and mechanisms of activation through ionotropic channels.
Discusses the dynamics of EPP, Na+ K+ movement, safety factor, and transmission efficacy in muscle synapses.
Details on synaptic termination processes, including diffusion, enzymatic degradation, reuptake, and roles of autoreceptors.
Factors affecting neurotransmission safety like quanta, receptor density, and enzyme activity.
Genetic disorders affecting Na+ and Ca2+ channels, including muscle and neurological diseases related to channel dysfunction.
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Neuromuscular transmission
- 4.
- 8. NMJ on themuscle fiber 10µm 10µm
- 10. Synaptic selectivity atdeveloping NMJ
- 12. Synapse from afrog sartorius neuromuscular junction showing vesicles clustered in the active zone, some docked at the membrane (arrows). (from Heuser, 1977)
- 13.
- 14. Synaptic Transmission Model • • • • • • Precursortransport NT synthesis Storage Release Activation Termination ~diffusion, degradation, uptake, autoreceptors
- 15.
- 16.
- 17.
- 18.
- 19. A quantum isthe number of transmitters released from a single synaptic vesicle Vesicles have a fairly uniform size and diameter ≈ 40- 50 nm Individual vesicles contain 8000 - 10,000 phospholipid molecules and several proteins. The vesicle molecular weight is approx. 3-5 x 106
- 21. Proteins associated withsynaptic vesicles (identified through sequencing and cloning of cDNA’s) Membrane proteins A. B. C. Synaptophysin (~ 36 kD) Synaptotagmin (~ 61 kD; the Ca2+ sensor) Snares (residents of either the vesicle [v-snare] or the target membrane [t-snare]) 1. VAMP (also called synaptobrevin), a v-snare (~18 kD) 2. Syntaxin, a t-snare that also associates with Ca 2+ channels (~32 kD; technically not a vesicle protein) 3. SNAP-25, a t-snare (~25 kD; also technically not a vesicle protein) D. Electrogenic proton ATPase -creates emf that drives neurotransmitter uptake against a concentration gradient
- 22. Proteins associated withsynaptic vesicles (identified through sequencing and cloning of cDNA’s) Membrane proteins A. B. C. Synaptophysin (~ 36 kD) Synaptotagmin (~ 61 kD; the Ca2+ sensor) Snares (residents of either the vesicle [v-snare] or the target membrane [t-snare]) 1. VAMP (also called synaptobrevin), a v-snare (~18 kD) 2. Syntaxin, a t-snare that also associates with Ca 2+ channels (~32 kD; technically not a vesicle protein) 3. SNAP-25, a t-snare (~25 kD; also technically not a vesicle protein) D. Electrogenic proton ATPase -creates emf that drives neurotransmitter uptake against a concentration gradient
- 23. An alternative formof Ca2+-dependent vesicle fusion, termed fast tracking, or “kiss and run” predominates at low frequency stimulation.
- 24. Life cycle ofa synaptic vesicle
- 27.
- 28.
- 29.
- 30.
- 31. From Kristin HarrisLectures. http://synapses.mcg.edu/lab/harris/lectures.htm
- 33. Stimulation mini Evoked amplitudes. 1X 4X Mini histogram. 2X 1X 3X 4X 2X 1mV Squire Fund. Neurosci.
- 34. From Kristin HarrisLectures. http://synapses.mcg.edu/lab/harris/lectures.htm
- 35. “docked” No firing “fast” “slow” Firing Heuser andReese, 1981 Electron micrographs of “omega figures” (fusing synaptic vesicles) after slam freezing a firing synapse provided clinching evidence for the vesicle hypothesis.
- 36. A cholinergic synapse Ne rv Action potential Choline ef ibe r( ax on ) Na+,Cl- Acetyl-CoA Acetyl-Choline Ca + + Ca + + Acetyl-Choline
- 37. A cholinergic synapse(2): Rapid transmitter inactivation by cholinesterase Choline Acetate Action potential Acetyl-CoA Acetyl-Choline Ca + + Choline esterase
- 38.
- 40.
- 41.
- 42.
- 43.
- 44. Acetylcholine Receptor α β γ (or ε) ACh ACh δ α Miyazawa, A.,Y. Fujiyoshi, and N. Unwin. 2003. Structure and gating mechanism of the acetylcholine receptor pore. Nature 423:949-955.
- 45. End Plate Potential(EPP) Presynaptic terminal VNa Muscle Membrane Voltage (mV) The movement of Na+ and K+ depolarizes muscle membrane potential (EPP) 0 EPP Threshold -90 mV VK Presynaptic AP Time (msec) Outside Muscle membrane Inside ACh Receptor Channels Voltage-gated Na Channels Inward Rectifier K Channels 45
- 46. Normal EPPs invariablyevoke muscle action potentials • Normally, the average EPP amplitude = 60 mV -In frog, ~150 vesicles • Safety factor for transmission is therefore high (greater than 1) - Frog example: ∆VEPP ÷ ∆VAPthreshold = 60 mV ÷ │-90 mV*- [-50 mV] │ = 60 mV ÷ 40 mV = 1.5 (*muscle resting VM = -90 mV)
- 47.
- 48.
- 49. (6.2) Termination by... Enzymaticdegradation
- 50. Acetylcholine Metabolism acetylcholine ACh esterase (AChE) choline +acetate • AChE is located in the synaptic cleft • Choline is taken back up into the presynaptic terminal – active process • Acetate diffuses away to be utilized in other metabolic roles
- 51.
- 52.
- 54. The Safety Factor!!! • Number of Quanta • The receptor density on the post synaptic membrane • The activity of ACH esterase • The folds of the PS membrabe • The presence of active zones
- 57.
- 58. Na+ channelopathies Gene Channel Disease Muscle SCN4A α subunitof NaV1.4 Hyperkalaemic periodic paralysis Hypokalaemic periodic paralysis Paramyotonia congenita Potassium-aggravated myotonia Myotonia fluctuans Myotonia permanens etc Neuronal SCN1A α subunit of NaV1.1 (somatic) Generalised Epilepsy with Febrile Seizures + (GEFS+), Severe myoclonic epilepsy of infancy (SMEI) SCN2A α subunit of NaV1.2 (axonal) GEFS+ SCN1B β1 subunit
- 59.
- 60. Ca2+ channelopathies Gene Neuronal Disease CACNA1S α subunitof CaV1.1 HypoK periodic paralysis Malignant hyperthermia RYR1 Muscle Channel Ryanodine receptor (sarcoplasmic channel) Malignant hyperthermia Central core disease CACNA1A α subunit of CaV2.1 (P/Q-type channel) Familial hemiplegic migraine Episodic ataxia type 2 Spinocerebellar ataxia type 6 Absence epilepsy? CACNA1H αsubunit of CaV3.2 (T-type channel) Absence epilepsy
- 61. Nicotinic receptor channelopathies Gene CHRNA1 α1subunit Congenital myasthenic syndrome β1 subunit CHRND δ subunit CHRNE Neuronal Disease CHRNB1 Muscle Channel ε subunit CHRNA2 α4 subunit CHRNB4 β2 subunit AD nocturnal frontal lobe epilepsy
- 62. Slow channel syndrome Sine etal (1995)
- 63. Fast channel syndrome canbe associated with congenital joint deformities (arthrogryposis multiplex) Brownlow et al (2001)
Editor's Notes
- #10 neuro4e-fig-08-11-0.jpg
- #38 Cholinesterase provides for a very rapid mechanism of inactivation. This makes acetylcholine a preferred transmitter where rapid modulation of the signal is desired. Example: Voluntary muscular action.
- #45 ACh: acetylcholine AChR: acetylcholine receptor is the nicotinic hetero(and penta)meric muscle form, which has (1)2,,, fetal subunit composition and (1)2,,, adult subunit composition
- #47 Endplate potentials (EPPs) are larger, compound MEPPs that result from the activation of many of the terminals of an endplate at the same time. The average EPPs results from the summation of ~150 average MEPPs. The average EPP amplitude is therefore ~+60 mV (0.4 mV/quantum X 150 quanta). If the resting VM of the muscle fiber is -90 mV and the threshold for action potential initiation is -50 mV, a single average EPP will provide 1.5X the voltage required to change VM to the action potential threshold! The normal “safety factor” for neuromuscular excitation is therefore quite high, ~2. That means that under normal circumstances, a muscle action potential will always be generated, and the muscle will contract, as a result of a single EPP. If the fiber is repeatedly stimulated over a very long period of time, some failures will be observed, because the axon will start to run out of vesicles and/or the muscle will fatigue.