mechanoreceptors one Flashcards

1
Q

nerve endings in glabrous skin

A

merkel cells
ruffini endings
pacinian’s’ corpuscle
meissner corpuscle
free nerve endings

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2
Q

what do nerve endings that terminate in your skin cause?

A

cause you to have tactile experiences

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3
Q

how did scientists identify somatosensory nervous system in c elegans

A

lesioned neurons one by one
after some lesions, the worm wouldn’t swim away, so it was concluded that these were neurons involved in somatosensation

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4
Q

O’Hagan et al (2004)
recording from neuron PLM, immobilised on microscope slide

A
  • intracellular electrophysiology, record membrane potential of a specific neuron
  • green fluorescent protein labelling of PLM cell, so we can see where to record from under fluorescent microscope

1) record from the cell
2) carefully touch the animal
3) response, receptor potential, ion channels open, sodium current

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5
Q

human mechano-transduction
what we knew and mechanism concluded

A
  • Response happens very quickly, therefore it cannot be a signalling cascade
  • Mechanical force acts directly to stretch membrane and open ion channels

Mechanism of touch signal transduction appears to be direct deformation of cell membrane

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6
Q

coste et al (2010)
whole cell electrophysiology
screen cell lines poke assay
mechanically activated current

A

cell on a dish, poke the cell, can record if there is any change in membrane potential when you poke the cell

found a cell line that does mechanoreception, it is helpful to study genetic mechanisms

must be one or more proteins expressed in the cell that are key players in mechanotransduction

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7
Q
  • DNA micro array
  • Small interfering RNA (siRNA) knock-down
  • Trying to find Piezol
A

tells you thousands of genes expressed in this cell

concluded it was meant to be a membrane spanning protein, bringing it down to a list o 75 candidates

inactivated proteins and repeated poke array technique, if they inhibit the protein involved, no receptor current would be produced

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8
Q

where was piezo 1 found?

A

mainly in internal organs, not the skin

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9
Q

ow was piezo 2 found?

A

When searching trough DNA database, they found structurally similar protein to piezo 1 that was expressed in the skin

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10
Q

how was it shown that piezo 2 is necessary and sufficient for mechanotransduction

A

if you express piezo 2 in a cell that doesn’t already express it, that cell should be able to produce mechanical receptor potentials
-found in cell lines, sufficient

If you have an animal where you inactivate it completely, they should become less or insensitive to touch
-completed poke rest on knockout mice (behavioural test)
-Piezo 2 is essential for mechano-transduction

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11
Q

somas of mechanoreceptors:

A

 body: dorsal root ganglion
face: trigeminal ganglion

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12
Q

DRG/TRG axon:

A

primary afferent fibre
peripheral branch (to extremities)
central branch (to the brain)

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13
Q

thin/ unmyelinated primary afferent fibre

A

axons related to our sense of pain

mechanical force has rapid effect, but tissue injury travels slowly to the brain

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14
Q

thick/myelinated primary afferents

A

action potentials propagate more quickly, so APs go faster to CNS

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15
Q

Adrian and Zotterman (1926)

A
  • insert electrode into part of nervous system you are interested in, electrode becomes sensitive to ions flowing across membrane, can measure action potential
  • can study the function of the neuron to see what it is sensitive to
  • discovered many types of primary afferent
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16
Q

low threshold mechanoreceptors are sensitive to

A

gentle touch

17
Q

high threshold mechanoreceptors

A

harmful, or potentially harmful, stimuli
nociception

18
Q

thermoreceptors

A

responsive to cold/ heat

19
Q

low threshold mechanoreceptors cutaneous nerve and myelination

A

Aα/Aβ cutaneous nerve
heavily myelinated

20
Q

nociceptive mechanoreceptors cutaneous nerve and myelination

A

Aδ/C cutaneous nerve unmyelinated or thinly myelinated

21
Q

thermoreceptive mechanoreceptors cutaneous nerve and myelination

A

Aδ/C cutaneous nerve unmyelinated or thinly myelinated

22
Q

receptive field of a fibre/ neuron

A

Receptive field of a fibre/ neuron: that area of skin, stimulation of which increases firing rate

there is diversity in of the receptive fields of mechanoreceptors (first dimension)

23
Q

slowly adapting neuron

A

lots of action potentials at first but it gradually slows down

24
Q

rapidly adapting

A

action potential fires when the stimulus starts and when it ends

25
Q

FA1

A

fast adapting
small, sharp boarder receptive fields

26
Q

FAII

A

fast adapting
large obscure boarder receptive fields

27
Q

SAI

A

slowly adapting
small sharp receptive field boarders

28
Q

SAII

A

slowly adapting
large obscure boarder receptive fields

29
Q

receptive field size of superficial nerve endings (epidermis)

A

small

30
Q

receptive field size of deep nerve endings in the dermis

A

large

31
Q

merkel cell

A
  • Polylobulated nucleus
  • Axon splits into subbranches
  • Close to the cell surface, it sheds its myelin sheath completely
    terminates in a round disc, which goes into a Merkel cell
  • Small receptive field
  • SAI type
  • 100cm2 (human fingertip)
32
Q

messiner’s corpuscle

A
  • Encapsulated structure, cap into which the axon enters
  • Schwann cell laminae
  • Small RFs
  • Rapidly adapting
  • FAI type
  • 150/cm2 (human fingertip)
33
Q

pacinian corpuscle

A
  • Encapsulated
    axon enveloped by schwann cells, much larger than the Messiner’s corpuscle
  • Less common than messiner’s corpuscle
  • Very large RFs
  • Rapidly adapting
  • PC (FAII)
  • Very sensitive
  • 10-15% of fibres in hand
34
Q

SAII fibres

A
  • Innervation unclear
    previously thought to be ruffini ending, more recent evidence has shown this is incorrect
  • Large RF
  • Slowly adapting
  • 20% of fibres in hand