Cell Communication SEM1 Flashcards

1
Q

What are gap junctions

A

Cell-cell junctions between apposed plasma membranes - direct connect for small soluble signals (not large molecules)

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2
Q

What signals are moved across membranes through vesicle fusion (exocytosis)

A

-proteins
-peptides
-amino acids
-nucleotides

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3
Q

What signals are released through channels and transporters

A

Ions

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4
Q

What does it mean for a signal to be released constitutively

A

Passive flow down concentration gradient

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5
Q

What does it mean for a signal to be evoked when released

A

Channels can be gated

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6
Q

What signals are released through free diffusion

A

Steroids
Gasses
(Both are hydrophobic)

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7
Q

What are the three main forms of signaling of secreted molecules

A

-paracrine
-synaptic
-endocrine

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8
Q

What is the action of signals released through paracrine signaling

A

Released signals only affect cells in the immediate cellular environment

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9
Q

How do signals terminate in paracrine signalling

A

-uptake into neighboring cells
-destruction by extracellualr enzymes
-sequestration by extracellular matrix

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10
Q

What is the action of signals released through autocrine signalling

A

The signal is released onto the same cell type

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11
Q

What can a group of identical cells in autocrine signaling result in

A

Group of identical cells produces a higher concentration secreted signal than a single cell can - 1 cell releases signal, binds to receptors on neighboring cells => amplify signal

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12
Q

What does the activation of the dendrite trigger in synaptic signaling

A

-activation at dendrite triggers electrical impulses (action potentials) along neuronal axon

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13
Q

What happens when an impulse reaches the nerve terminal in synaptic signalling

A

It stimulates secretion of chemical neurotransmitters

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14
Q

What is the role of endocrine cells

A

Secrete signals - hormones - into the blood

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15
Q

How is specificity of signalling maintained in endocrine signalling

A

Only certain cells have appropriate receptors to recognise specific hormone

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16
Q

How can specificity of signalling be achieved by synaptic signalling

A

Arises from the physical location of the signalling site and the receptor

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17
Q

How can specificity of signalling be achieved by endocrine signalling

A

Arises from combination of different signalling molecules being recognised by equally array of receptors (wide range of signals and receptors)

18
Q

What is the difference in distance travelled by endocrine and synaptic signalling

A

-endocrine targets anywhere in body - long distance
-synaptic targets 100nm away from signal -short distance

19
Q

What is the difference in speed between endocrine and synaptic receptors

A

-endocrine realised on diffusion and blood flow to reach target - slow
-synaptic signals take <1 sec to reach target - fast

20
Q

What is the difference between the affinity of target between endocrine and synaptic signalling

A

—endocrine signals diluted in bloodstream - receptors high affinity
-synaptic signals highly concentrated at synapse - receptors low affinity

21
Q

Which cells do not require receptors

A

Cells that use signalling via gap junctions or gasses

22
Q

What does binding of the signal (ligand) cause

A

Receptor activation

23
Q

What does receptor activation stimulate production of

A

Stimulates production of intracellular signals

24
Q

Where are receptors located in relation to steroid signalling

A

Receptors located within the cell

25
What are the 4 major types of receptors
-ionotropic -metabotropic -kinase -steroid
26
Function of ionotropic receptors
Allow flow of ions across membranes
27
Function of metabotropic receptors
Generate new signals inside cell (2nd messengers)
28
Function of kinase receptors
Modify existing molecules to generate new signals
29
Function of steroid receptors
Change expression of genes
30
What effect can ionotropic receptors induce
Changing the membrane potential
31
What are the two types of ionotropic receptors
Excitatory - influx of positive charged ions e.g Na+ or Ca2+ Inhibitory - influx of negative charged ions e.g Cl-
32
How do metabotropic or G-protein-linked receptors act to regulate the activity of a plasma-membrane-bound target protein
The receptors act indirectly to a target which is either an enzyme or an ion channel
33
What is the intermediate between the receptor and target in metabotropic processes
A trimeric G-protein
34
What are the 3 subunits of G-proteins
Alpha (a), beta (B) and gamma (y) subunits
35
What do the subunits of g-proteins bind to
Bind to metabotropic receptors which have 7 transmembrane domain structures (Metabotropic and G protein linked receptors have same structures)
36
How is the G-protein attached to the receptor and membrane
Attached to receptor by its alpha (a)- subunit Attached to membrane by its alpha(a) and gamma(y)-subunits
37
What does the ligand binding cause the alpha(a subunit to release
Releases GDP for GTP (gtp replaces gdp and binds to alpha subunit of protein)
38
What does ligand biding and the a-subunit release of GDP and GTP cause
1)activation of the alpha(a) subunit and 2)release of the beta(B)/gamma(y) subunits
39
What does the activation of the alpha-subunit allow for
To alter enzyme activities therefor change concentration of intracellular signals inside cell
40
How is signalling from metabotropic receptors terminated
Terminated by hydrolysis of GTP to GDP by the alpha-subunit
41
What are kinase receptors
Either enzymes themselves or associated with enzymes
42
What is the structure of a kinase receptor
One transmembrane domain with a ligand binding site outside the cell and enzyme activity inside cell