DLA #4: Membrane Structure and Transport Flashcards
(36 cards)
Lipid Rafts are:
Dynamic assemblies of lipids and proteins
Lipid Rafts play a role in:
Signal transduction and virus infections
Planar lipid rafts are:
- formed by cholesterol, glycolipids and sphingomyelin
- they are short lived
Caveola are
- Also lipid rafts
- Form invagination of the pm
- Long lived -Stabilized by caveolins
Explain what happens to fatty acid tails when exposed to a cold environment. What homeostatic response occurs
- Fatty acid tails stiffen up
- Cholesterol will intercalate itself b/w phospholipids and increase membrane fluidity.
Explain what happens to fatty acid tails when exposed to a hot environment. What homeostatic response occurs
- Fatty acid tails begin to loosen up and become more fluid.
- Cholesterol will use its steroid ring system to decrease fluidity.
What are lipoproteins
Proteins that transport nonpolar lipids through the blood/lymph.
Describe the characteristic traits of a lipoprotein
- Hydrophobic core
- Hydrophillic shell.
- Transfers TAG and cholesteryl ester.
How do membranes inside the cell regulate fluidity
Membranes inside the cell DO NOT have cholesterol.
Therefore, regulation of fluidity is based upon the fatty acid composition of that membrane.
Passive transport through a membrane includes:
1) Simple Diffusion (Moves down gradient through pm)
2) Faciliated DIffusion (Moves down gradient through a channel/transporter)
Cell w/in out body take in Glucose via:
Glucose Transporters aka GLUT
(multiple in body for select area)
GLUT is a good example of what type of diffusion
Faciliated.
List out the high affinity GLUT transporters:
GLUT-1, GLUT-3, GLUT-4
List out the low affinity transporters
-GLUT-2 and GLUT-5
During normal or lower blood glucose levels in general circulation we expect
-GLUT-1 and GLUT-3 to be working at a constant rate
GLUT-1 is found in
RBC’s, BBB and Kidneys
GLUT-3 is found in:
Neurons and the brain
What is hereditary GLUT-1 deficiency
- form of metabolic encephalopathy
- as infants develop growth of brain and skull is slowed
- Symptoms include:
- Epileptic-Seizures
- Ataxia
- Delayed psychomotor development
- Movement disorder
- Speech Disorder
***Symptoms become more prevalent w/ age
What is a way in which we can evaluate if someone has GLUT-1 Deficiency
Taking a sample of the RBC’s
What is really unique about GLUT-2:
Its a TWO way transporter.
Where are GLUT-2 transporters usually found:
1) Intestinal Mucousal cells => Glucose gets transferred via GLUT-2 into the portal vein
2) Hepatocytes => Liver is the glucose banks. It both stores glucose during levels of high glucose in circulation and gives off stored glucose during fasting. It can even make new glucose during serious starvation. Therefor we expect a two way GLUT portal to be available.
3) Pancreatic B-cells => Beta cells have GLUT - 2 in order to test the amount of glucose in general circulation and determine if release of insulin is necessary.
4) Renal tubular cells. => In the renal syste, both reasorption and secretion of glucose occurs. Therefore, a two way portal is needed. Not only that, kidneys do very little gluconeogensis, therefore we expect the kidney’s to also have GLUT-2.
Explain a little more about why GLUT-2 is used to measure glucose levels in regards to B-cell functioning:
GLUT-2 is used by Beta cells of the pancreas to “taste” glucose levels in the general circulation.
These GLUT-2 are so important b/c the pancreas needs to know when it’s the right time to release insulin for uptake of glucose into our adipose and skeletal tissue cells.
****Document attached goes even more in depth
Where is GLUT-4 found and what is its function
- Adipose
- Skeletal
- Heart
What signals can cause a cell to release GLUT-4
- High levels of Glucose in general circulation
- ALSO, during vigorous excercise