Block 2 Lecture 17 Flashcards

1
Q

what are the two sides to a plasma membrane

A

basolateral and apical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

where is the basolateral side located

A

the blood side of the layer and is exposed to ISF

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

where is the apical side located

A

outside of the body such as the lumen of intestines)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is an exception to the apical side of the membrane

A

choroid plexus where the apical side is exposed to the cerebrospinal fluid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what are the principle barrier epithelia that line organs that have large surfaces exposed

A

GI tract, kidney nephron, and liver (other significant are choroid plexus, retina and exocrine glands)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what are the 2 types of pathways for transport

A
paracellular = between adjacent cells
transcellular = across individual cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what happens in paracellular transport

A

molecules move through tight junctions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what are tight junctions

A

a complex of proteins that attach cells to one another

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are the functions of tight junctions

A
  1. ) barrier that reduces free diffusive movement of molecules via the paracellular pathway.
  2. ) provides a barrier to prevent mixing of molecules between basolateral and apical membranes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

where are tight junctions located in between cells

A

typically closer to the apical side

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what size molecules can pass through tight junctions

A

any molecule less than 4A (glucose is slightly larger)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what do claudins do

A

establish the permselective character of tight junctions and form aqueous pores of about 4A

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

claudins that form pores that contain a surplus of cationic residues in the postulated pore forming region have been found to favor the paracellular movement of what?

A

anions such as Cl-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

claudins that form pores that contain a surplus of anionic residues in the postulated pore forming region have been found to favor the paracellular movement of what?

A

cations such as Na+

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are zymogens released by in the pancreas?

A

secretagogues

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what are the 4 types of secretagogues

A

CCK, ACh, VIP, and secretin (CCK and ACh most important)

17
Q

how do CCK and ACh work

A

by binding to the G protein coupled CCK receptor or the muscarinic ACh receptor which activates protein kinase C (PKC) producing an increase in intracellular Ca2+

18
Q

how does VIP and secretin work

A

they bind to different receptors that stimulate PKA to release zymogens

19
Q

what “help” zymogen granule release (SSC)

A

SNARE proteins, Rab proteins, and synaptotagmin

20
Q

what do SNARE proteins do

A

there are more than 60 SNARE proteins expressed in cells to get right vesicles to fuse in right place. there are v-SNARES and t-SNARES

21
Q

what do Rab proteins do

A

they are small G proteins the bind and hydrolyze GTP that help assemble SNARE fusion complex. there are about 70 Rabs which aid in targeting specificity

22
Q

what are synaptotagmins proteins and what do they do

A

they are integral membrane proteins in vesicle membranes. they bind Ca2+ and once activated can stimulate the fusion event in exocytosis. 15 synaptotagmins involved in vesicle fusion in different cell types

23
Q

why is SSC energetically unfavorable

A

because when vesicle membranes and plasma membrane get close to each other they repel because they are both negatively charged

24
Q

what happens in acinar cells of the exocrine pancreas

A
  1. ) driven by Na,K ATPase in basolateral membrane
  2. ) Na+ gradient drives accumulation of Cl- from blood into acinar cells via Na,K, 2Cl cotransporter
  3. ) Cl- moves from acinar cells into lumen through apical Cl- channel because of inside negative membrane potential
  4. ) trans epithelial secretion of Na+ relies on paracellular pathway. Cl- moving into lumen makes it negative providing electrical force to support paracellular diffusion of Na+ through tight junction
  5. ) increase in NaCl in lumen supports osmotically driven flux of water via aquaporins
25
Q

what results in inside negative membrane potential

A

outwardly directed K+ gradient

26
Q

how is the Na, K, 2Cl con transporter electrically neutral

A

because there’s a flow of 2 cations (1 Na+ and 1K+) and 2 anions (2Cl-)

27
Q

what does the apical Cl- channel open in response to

A

activation of PKC by CCK or ACh

28
Q

what happens in duct cells in the exocrine pancreas

A
  1. ) driven by Na,K, ATPase
  2. ) basolateral HCO3- entry involves Na/HCO3- cotransporter
  3. ) HCO3- is secreted into lumen via Cl-/HCO3- exchanger
  4. ) the Cl- that enters the cell via Cl-/HCO3- exchanger exits the cell back into lumen via 2 Cl- channels: CTFR and ORCC
  5. ) the cycling of Cl- keeps ductal lumen negative supporting paracellular diffusion of Na+
  6. ) net flux of NaHCO3 results in osmotic flux of water into lumen. this flow pushes zymogens into small intestine