Plasma Lipoproteins Flashcards

1
Q

what is the function of lipoproteins?

A

functions

  • to transport ipids to and from tissues
  • to keep their lipid components soluble for transport in the plasma
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2
Q

what is the most dense lipoprotein? Least dense?

A

most dense= HDL

least dense = chylomicrons

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3
Q

there is a high concentration of cholesterol and cholesterol esters in which lipoprotein?

A

in the LDLs

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4
Q

what is the function of apolipoproteins?

A

structural components and ligands for cell-surface receptors

  • coenzymes for lipid metabolism enzymes
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5
Q

what are the five major classes of apolipoproteins and their subclasses?

A

apolipoprotein A,B,C,D,E

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6
Q

how are dietary lipids transported throughout the body?

A

by chylomicrons

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7
Q

describe how Chylomicrons are made and destroyed?

A
  1. apolipoprotein synthesis- in rough ER
  2. lipid synthesis- of TG, cholesterol, phospholipids in smooth ER
  3. chylomicron assembly in Golgi apparatus -
  4. maturation - in blood plasma - given Apo C and E from HDLs
  5. utilization of chylomicron TG by tissues- by activation of lipoprotein lipase (by Apo C/C2)
  6. clearance of chylomicron remnants (no Apo C present anymore, but Apo E is exposed) - Apo E recognized by liver and remnants are sequentially destroyed
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8
Q

what is the purpose of Apo C and Apo C2? How about Apo E ?

A

Apo C /C2 activate lipoprotein lipase in tissues and allow for extraction of TGs from the chylomicron

Apo E is recognized by liver receptors

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9
Q

What is the purpose of VLDL, LDL and HDL in the body?

A

VLDL = transport endogenously synthesised TG

LDL= tranport endogenously synthesized cholesterol

HDL = transport cholesterol from tissues to liver

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10
Q

Describe the synthesis and degradation of VLDLs

A
  1. made in liver by process similar to chylomicrons
  2. secreted into circulation - pick up ApoC/E from HDL
  3. TG contained in VLDLs is degraded by Lipoprotein lipase
  4. as TGs are removed, VLDL gets smaller and more dense- eventually becoming LDLs once they lose their ApoC/E
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11
Q

what is the purpose of LDLs?

A

delivery of cholesterol to the peripheral tissues by receptor mediated endocytosis via LDL receptor

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12
Q

what does the LDL receptor recognise?

A

it recognizes (Apo B-100) and (Apo E)

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13
Q

what does the LDL receptor NOT recognize?

A

Apo B-48

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14
Q

how do macrophages become foam cells?

A

they eat too many oxidised LDLs

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15
Q

what can foam cells lead to?

A

atherosclerotic plaque

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16
Q

how are HDLs synthesised?

A

they are formed in the blood by addition of lipids to apolipoprotein Apo A1 which is synthesised by liver and small intestine and develops into nascent HDL

17
Q

what is the function of HDL cells?

A
  • reservoir of apolipoproteins C/E
  • accumulating unesterified cholesterol
  • rapid esterification of cholesterol
  • reverse cholestrol transport - very important
18
Q

why does cholesterol need to be transported back to the liver?

A

for conversion to bile salts

excretion of bile

and use in steroid synthesis

19
Q

Hypertriglyceridaemia is a disorder of what?

A

of VLDL and chylomicrons

  • lipoprotein lipase deficiency = lack of metabolism of TG
  • apoprotein C2 deficiency = no activation of LPL
20
Q

hypercholesterolaemia is a disorder of what?

A

of LDLs

  • lack of LDL receptor in heterozygous familial hypercholesterolaemia
  • apoprotein B100 gene mutation - required for bindin gLDL to receptor
  • polygenic hypercholesterolaemia - most high cholesterol cases
21
Q

Tangier disease is a disorder of what?

A

of HDLs

it is a mutation of the ABCA1 gene - leads to low plasma HDL cholesterol and accumulatio of cholesterol in tissues

22
Q

what is familial autosomal dominant HDL deficiecy?

A

ABCA1 gene mutation - leads to low HDL levels

23
Q

what is the most common patient group for hyperlipidaemia

A

polygenic - increased risk of CV disease due to high LDL levels and suppression of HDL by high TG levels