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3 Mar 2018

When would you need one form of cell signaling versus another? What're the costs/benefits?

(Thinkning about: Direct, Autocrine, Paracrine, and Endocrine Signaling; as well as Signal transduction pathways like Ligand-gated ion channels, Receptor enzymes, G-protein coupled receptors, and Intracellular receptors)

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Collen VonLv2

6 Mar 2018

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Related questions

1. How does sexual reproduction compare to DNA transfers inprokaryotes?
I. Both increase genetic diversity.
II. Sexual reproduction results in greater evolutionarychange.
III. DNA transfer in prokaryotes allows for fewer errors andmutations.

a. I only

b. I and II

c. I and III

d. I, II, and III

2. What type of receptor is described in the followingparagraph?

Binding of a signaling molecule to this type of receptor uses anenzyme to remove a phosphate group from an ATP molecule to activateanother receptor. The activated receptor can be recognized by relayproteins inside the cell, which bind to the receptor and changeshape. These activated proteins then trigger a transduction pathwaythat leads to some sort of cellular response.

a. intracellular receptor

b. ligand-gated ion channel

c. g protein-coupled receptor

d. receptor tyrosine kinase

3. Yeast cells, plant cells, and mammal cells all share manysimilarities in cell signaling. This provides evidence that

a. cell-signaling mechanisms are only found in organisms that usemethods of sexual reproduction

b. intercellular communication evolved as a way for multicellularorganisms to coordinate cell functions

c. eukaryotic cells use signal transduction pathways whileprokaryotic cells use a more primitive form of signaling

d. signal transduction pathways appeared in cells before theevolution of multicellular organisms

limehornet465

The insulin receptor is a
a. phosphatase.
b. kinase.
c. phosphodiesterase.
d. cAMP molecule.
e. G protein.

What do the following receptors all have in common: G protein-linked receptors, protein kinases, and ion channels?
Select one:
a. Conformational change once the ligand is bound
b. Ligand binding
c. Amplification of the signal
d. All of the above

Diacylglycerol
Select one:
a. activates G proteins.
b. hydrolyzes phosphatidyl inositol-bisphosphate.
c. is released from the cell as a paracrine-signaling molecule.
d. opens Ca2+ channels.
e. activates protein kinase C

Gap junctions
Select one:
a. permit metabolic cooperation among linked cells.
b. are present on few copies per cell.
c. contain membrane lined bridges.
d. are channels about 1. 5 mm in diameter.
e. allow large molecules and ions to pass rapidly between cells.

Smooth muscle cells in the airways relax while those in the blood vessels contract in response to the hormone epinephrine. What would you expect to be different in these two types of cells exposed to epinephrine?
Select one:
a. Presence of epinephrine receptors.
b. Exposure to epinephrine released by neighboring cells.
c. Activation of protein kinases.
d. Rate of metabolism.
e. Types of proteins expressed.

The second messenger IP3
Select one:
a. is released from the cell as a paracrine-signaling molecule.
b. hydrolyzes phosphatidyl inositol-bisphosphate.
c. activates protein kinase C.
d. opens Ca2+ channels.
e. activates G proteins.

sangriaskunk539

Tetraethylammonium (TEA) is a drug that blocks voltage-gated potassium channels. What effect would this have on an action potential?

(a)Prevent the rising phase

(b)Prevent the cell from reaching the threshold to trigger an action potential

(c)Prevent or prolong the falling phase

(d)None of the above

The hyperpolarization phase of the action potential is due to:

(a)The opening of voltage-gated Cl- channels

(b)Prolonged opening of voltage gated K+ channels

(c)The closure of resting Na+ channels

(d)Rapid inactivation of voltage-gated K+ channels

The period when it is difficult to initiate another action potential for several milliseconds due to voltage-gated sodium channel inactivation is referred to as the:

(a)Relative refractory period

(b)Absolute refractory period

(c)Resting period

(d)Hyperpolarization period

In the human central nervous system, Gap junctions are found:

(a)Only between neurons

(b)Only between astrocytes

(c)In both neurons and astrocytes

(d)In all cells

Small molecule transmitters such as acetylcholine are synthesized in:

(a)The nerve terminal

B) The cell body and transported to the nerve terminal

C) Synaptic vesicles

D) Endoplasmic reticulum

Prior to Otto Loewiâs classical experiment, which of the following was not known:

(a)stimulation of the vagus nerve slows the heart

(b)extracts of frog heart, made following vagal nerve stimulation, slow the heart

(c)some acetylcholine effects are similar to those produced by muscarine

(d)vagal nerve stimulation releases a substance which slows the heart

Which of the following is most important in determining if neurotransmission is excitatory or inhibitory?

(a)The structure of the synapse

(b)The neurotransmitter released by the presynaptic neuron

(c)The neurotransmitter receptor

(d)The strength of the stimulus

Benzodiazepines such as Valium allosterically regulate GABA receptors by:

(a)Binding at receptor sites other than the transmitter binding site

(b)Binding at the transmitter (GABA) binding site on the receptor

(c)Blocking the action of the endogenous transmitter

(d)Mimicking the action of the endogenous transmitter

GABA-A receptors are ligand-gated Cl- channels. The equilibrium potential of Cl- is -65 mV. At the neuronal resting membrane potential of -65 mV, GABA binding to the GABA-A receptor would result in the opening the Cl- channel, resulting in:

(a)no net flow of Cl- ions

(b)Cl- inflow and hyperpolarization

(c)Cl- outflow and depolarization

(d)Cl- outflow and hyperpolarization

At the mammalian neuromuscular junction, the released neurotransmitter acts on:

(a)muscarinic receptors

(b)nicotinic receptors

(c)adrenergic receptors

(d)Beta receptors

Neurotransmitters are packaged into synaptic vesicles by:

(a)endocytosis following transmitter release

(b)presynaptic membrane transporters

(c)vesicular transporters

(d)all of the above

. Which of the following are NOT types of ion channels?

Voltage-gated

(a)Ligand-gated

(b)G protein coupled receptor (GPCR)-gated

(c)Leak channels

(d)NONE of the above

NMDA receptors are unique in that their ion channel is:

(a)Ligand-gated

(b)Voltage-gated

(c)Ligand- and voltage-gated ion channels

(d)GPCR-gated

. Which of the following is INCORRECT regarding Catecholamine neurotransmitters

(a)Includes Dopamine, Norepinerphrine, and Epinephrine

(b)Contain a Catechol Ring

(c)Synthesized from Tryptophan

(d)Are produced by neurons whose cell bodies are located in the upper brainstem

The largest and most diverse group of receptors in eukaryotes is:

(a)Ligand gated receptors

(b)Glutamate receptors

(c)G-Protein coupled receptors

(d)Allosteric receptors

The most abundant G-protein coupled receptor in the brain is:

(a)Glutamate receptors

(b)Acetylcholine receptors

(c)Cannabinoid receptors

(d)Dopamine receptors

Which of the following drugs DOES NOT block voltage-gated Na+ channels

(a)Lidocaine

(b)Riluzole

(c)Reserpine

(d)Tetrodotoxin

Sarin, a nerve gas, exerts its toxicity by:

(a)blocking nicotinic receptors

(b)inhibiting choline acetyltransferase

(c)inhibiting acetylcholinesterase

(d)inhibiting voltage-gated Na+ channels

Botulinum Toxin (BoTox) interferes with transmitter release by:

(a)cleaving protein(s) involved in transmitter release

(b)blocking voltage-gated Ca2+ channels

(c)blocking voltage-gated Na+ channels

(d)blocking voltage-gated K+ channels

Atropine is:

(a)An agonist of the acetylcholine ionotropic receptor

(b)An antagonist of the acetylcholine ionotropic receptor

(c)An agonist of the acetylcholine metabotropic receptor

(d)An antagonist of the acetylcholine metabotropic receptor

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