Lecture 16 - Signal Transduction Mechanisms and Receptors Flashcards

1
Q

1) what are types of signaling mols?
2) Where can the receptors be located?
3) What is the result of interaction btw signaling mols and receptors?

A

1) hormones, ligands, neurotransmitters, GFs
2) cell surface or intracellular
3) can alter ion transport, metabolism (control pts), gene expression (turn on/off), and cell movement (across surface, muscle contractions)

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2
Q

What are the 4 modes of intercellular signal transduction?

A

juxtacrine, endocrine, paracrine and synaptic

***chemical mechanisms of transmmission

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3
Q

Define juxtacrine

Describe juxtacrine transduction

A

relative distance btw 2 cells interacting

sender cell expresses polypeptide/macromol on surface –> interacts with receptor on target cell –> causes some change inside cell (pathways, concentrations)

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4
Q

Describe endocrine transduction

A

sender cell secretes hormone that diffuses into blood vessel –> travels long distances and binds with receptor on target cell –> causes change

***long distance communication

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5
Q

Describe paracrine transduction

A

similar to endocrine but interacting with target cell close by

sender cell secretes local mediator (mol) –> binds with receptor on target cell –> causes change inside cell

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6
Q

Describe synaptic transduction

A

sender neuron has neurotransmitters at terminal end of nerve –> they are released and travel across gap (synapse) and bind to recepors on target cell –> causes change in cell

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7
Q

True or False:

1) Cell types only have receptors for 1 hormone
2) All Hormones have receptors in only 1 tissue
3) Some hormones have receptors in more than one tissue

A

1) False - some cell types have receptors for multiple hormones
2) False - some hormones have receptors in only 1 tissue
3) True

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8
Q

Name some cells and the signaling mols they secrete

Are these metabolic signaling mols highly regulated?

A

1) Pancreatic A cells - glucagon (polypeptide)
2) Pancreatic B cells - insulin (polypeptide)
3) Adrenal cortex - cortisol (steroid - small hydrophobic mols derived from cholesterol)
4) Adrenal medulla - epinephrine (catecholamine - derived from simple AA, tyrosine)

yes, their synthesis and secretion are highly controlled and their destruction is usually swift (in liver)

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9
Q

What common signaling mols interact with intracellular receptors?

Explain the interaction with an intracellular receptor

A

steroids, thyroid hormones

1) steroid can simply diffuse across membrane –> interacts with receptor in cytoplasm –> receptor/steroid complex is translocated to the nucleus –> acts as txn factor and alters gene expression

***steroids can target certain cells/tissues based on nature of which receptor is expressed

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10
Q

What type of signaling mols interact with cell surface receptors?

Explain the interaction btw these type of receptors and signaling mols?

A

hydrophilic hormones, neurotransmitters, GFs

1) hormone binds with receptor on cell surface –> change in concentration of certain mols inside cytoplasm (second messengers)

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11
Q

What is a second messenger?

Give some examples

A

substance which changes in concentration in the target cell in response to receptor activation

1) Ca+ - highly controlled, typically low in concentration
2) cAMP - derived from ATP, most important 2nd messenger
3) cGMP - derivde from similar mechanism as AMP
4) diacylglycerol and inositol trisphosphate - derived from phosphotidalinositol

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12
Q

1) What’s a protein kinase?
2) What’s a protein phosphatase?
3) Do these gene families portray substrate specificity?
4) What do these action do to protein?
5) Where are these enzymes located?

A

1) uses ATP to phosphorylate OH groups of AAs with hydroxyl side chains –> puts a P gp on
- Serine, threonine, tyrosine
2) dephosphorylate these side chains - takes P gp off
3) yes
4) (de)phosphorylation changes activity or function of protein
5) at key metabolic/fn control points

***control cellular activities by controlling [] of 2nd messengers

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13
Q

Name the types of cell-surface receptors

A

1) ligand-gated ion channel receptor - shut most of time –> ligands bind to receptor –> channel opens up and ions may flow thru
2) enzyme-linked receptors - several subunits become associated when hormone binds to binding sites (binding sites on each subunit) –>Activates catalytic domain on subunits
3) cytokine receptors - several subunits come together with binding of mol –> subunits bind to another enzyme which activates it
4) G-protein coupled receptors - 7 transmembrane domain receptor binds neurotransmitter or hormone –> interaccts with G protein –> activates G protein –> interacts with enzyme and activates it –> changes [] of 2nd messenger

*one of most abundant gene families

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14
Q

1) describe signaling by protein phosphorylation
2) describe signaling by GTP-binding regulatory protein

A

1) hormone receptor activates kinase –> transfers P gp from ATP to intracellular protein –> activates it –> causes change in cell –> eventually phosphatase is activated –> takes P gp off –> intracellular protein becomes inactive
2) hormone receptor interacts with G protein –> release GDP and binds new GTP –> activates G protein –> activates something/causes change –> GTP hydrolysis (takes P off GTP) –> inactivates G protein

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15
Q

What are the two main points about receptor - ligand interaction?

A

1) takes very low concentrations of ligands to bind to their receptors
2) good amount of cellular response can happen with only a fractino of receptors bound/activated

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16
Q

What happens when there’s a prolonged activation of synapse?

A

if structures stay open too long (activated state), receptors have mechanisms to prevent this –> channel will close to prevent prolonged ion flow (closed channel with neurotransmitters still bound