Lecture 11 - Hearing, touch, movement and balance Flashcards
What are some of the main features of mechanosensation?
- can determine between strong and soft stimulus
- 1 of the 5 basic senses
- mechanosensory neurons generate very rapid ionic currents in response to touch
- likely via direct gating initiated by hairs on the skin
- TREK, TRP, Degenerin/Enac and Piezo are the channels involved
- can adapt to touch
What are the neurons assocaited with touch and how were these established
Type II, non ciliated
-Multidendritic neurons (nociceptor neurons, muscle stretch receptos, visceral stretch receptor)
Type I, cilliated
-Bristles (macrochaetes, microchaetes, contact chemoreceptors, hair plates)
-Campaniform sensilla (haltere, wing)
-Chordotonal organs (Johnstons organ, fermoral ch organ)
Established via touching flies, worms and looking at response
What are the features of touch in c.elegans?
- can distinguish between soft, hard, nose and sexual touch
- stretch receptors just below the surface (in hypodermis)
- dendrites cover the body surface
- Neurons involved: e.g. PLM (body touch neuron),PVM, PVD, ALM, AVM
- force is convered directly through contact with the body wall, through the deflection causing movement of a 2 branched structure (in menorah cells), causing the opening of channels
- must be sufficent todepolarise touch sensitive neurons
- only lateral movement across these linear structure will generate a potential in a dendrite
- current carried by MEC-4 transduction-channel complexes
What are the features of touch in Drosophila?
-‘bristle morphology’ = sense touch/movement through dedicated groups of cells arranged to detect mechanical force through movement of a hair cell or stretch receptors
-bristle movement deforms the dendritic sheet of 2 mechanosensory neurons, leading to neuronal excitiation
-
What are the features of the development of mechanical sensation detecting organs in drosophila
-arise from simple developmental program including assymetyric cell division
1-neuroblasts [pI/SOP] (which have stem cell characteristics) divide, and one of the daughter cells recieves a set of proteins
2-a gradient of extracellular protein (notch - secreted) defines the cellular characterisation
3-other daughter cell lacks proteins
-cells known as either PIIb or PIIa
-a combination of intrinsic and extrinsic signals give rise to different types if sensory organs that are mechanosensitive:
-either hair cell (omat, chordatonal stretch receptor or mechanosensitive multidendritic cells)
Why are cillia critical in the struture of the extrasensory bristle and chordotonal organ? [drosophila]
-tubular bundle connects to the cillium
in chordotonal organ they must be connnected apically and basally to tightly packed microtubules
What are NomPA and where are they found? [drosophila]
NOMPA
-dendritic cap protein
-large extracellular domains which extend outside the cell and attach to the ECM
NOMPC
-TRPN protein
-29 ankyrin repeats enabling it to bind to other proteins (and therefore anchored in the membrane)
What type of TRP channel is only in the chordotonal organ and not the extrasensory bristle? [drosophila]
TRPV channels
What about the structure of the extrasensory bristle and chordotonal organ suggests they are used in hearing? [drosophila]
long, stiff filament shape
What is the Johnson’s organ and what is it for?
- at the front of a fly’s head
- for hearing
- similar to sense organs (extrasensory bristle, chordotonal borgan) but some different structures e.g. dendritic cap
- large extracellular structure linked to a channel in the membrane via a domain motif, then to the cytoplasm
How was touch observed experimentally in C.elegans?
- generate (through chemical mutagenesis) then identify mutants defective for a mechanosensitive response
- those identified were kept, bred and retested
- genetic mapping used to characterise, clone and identify mutants: through…
recombination with the strain in which the mutations have been induced against a related strain, and mapping of the mutant phenotype for cosegregation with known markers (e.g. SNP)
How does the ability to sense touch help C.elegans in their natural environment?
Helps to escape from predatious fungi
What are the structural conclusions from cloning ions of C.elegan mutants?
The molecular model of touch
- Mec-4 + 10: DegIENAc forms isoforms which act as pae forming units (channel normally has 2 Mec-4’s and 1 Mec-10)
- Mec-2 + 6: accessory subunits that enable channel activity
- Mec2: stomatin like protein on the inner leaflet of the membrane
- Mec-6: paraoxonase like transmembrane protein
What are the features of the specialised cytoskelton componetnts necessary for mechanotransduction? [drosophilla, c.elegans]
ECM -MEC-5: a collagen isoform -MEC-1 + 9: have multiple EGF repeats Below membrane Mec7 + 12: tubular monomers that form 14-protofilament microtubules
What anchors mechanosensitive channels to the ECM, and what are the features of these channels? [drosophilla, c.elegans]
- ECM proteins
- probably Na+ gated (potentially also K+)
- when exposed to movement will generate an action potential by shifting and therefor being gated
What part of the mechosensitive channel is directly involved in the gating mechanism? [drosophilla, c.elegans]
-the cystein rich domains are involved in the gating mechanism
What happens if the alanine residues in mechanosensitive channels are mutated to Valine residues? [drosophilla, c.elegans]
If alanie residues are mutated to Val
- the gate is always open
- leading to neurodegeneration
What is the model of mechanotransduction? [drosophilla, c.elegans]
Mechanotransduction involves:
a molecular assembly linking ECM to ion channel, which is linked to microtubules in the cytoskeleton
-movement gates the channel
What are other ways mechanosensitive channels can be activated? [not all channels are gated by mechanical deflection] And which channels use these mechanisms? [drosophilla, c.elegans]
TRP channels:
throught to be activated by many mechanisms that change the shape of the membrane to gate the channel
-membrane deformation: via pressue (pushing down on membrane), cell swelling or stress within the membrane itself
-2nd messengers: signals from other recpetors/channels activate these TRP channels
-biochemical deformation: 2nd messengers alter the bilayer composition, and potentially the phospholipds themselves
What are the features of mammalian touch?
- via hair structures
- different types of hairs with different neurons
- have lanceolate endings, merkel cell-neurite complexes, rufflini endings and free nerve endings that innervate the skin
- different receptors have different neuronal outputs (classified via these outputs through electrophysiological recording)
What are the neuronal outputs of the different receptors involved in mammalian touch?
Lanceolate ending: -down hair (Neurotropin-4 dependent) -Rapidly adapting Free nerve endings: -C-fibre (RunX1 or TrkA dependent) Merkel cell-neurite complexes: -Slowly adapting type 1 (Atoh1 and TrkC-dependent) Pacinian corpuscle: -rapidly adapting
What are the features of the different neuronal outputs involved in mammalian touch?
Rapidly adapting:
-apply stimulation, sudden signal, then shuts off
Slow adapting:
-found all throughout skin, keep firing to long time (type I specifically innervate some hair cells)
-stretch receptive
-irregular fibre pattern during sustained pressure
C-fibre:
-slow transduction , not a strong signal (fibre has a small diameter)
Down hair:
-basket like structure around the hair itself
-sensitive to light touch
What are the different classes of molecular channels and associated proteins in mammalian mechanosensastion?
- tranduction channels
- stomatin-like proteins
- Voltage gated K+ channels
- Voltage gated Na+ channels
- Two pore K+ channels
- TRP channels
- Acid-sensing ion channels
What is the mechanism of mechanotransduction in mammals?
- transduction channels convert force into receptor currents
- these trigger action potenials by opening voltage gated Na+K channels
- this signal travels to the brain to alert the organism to the force of the stimuli
Also dictated by ion channels that signal or set the membrane excitability (Two-pore K+ channels, TRP channels, acid sensing ion channels)