Apolipoproteins or lipoproteins Flashcards

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1
Q

Mediates remnant uptake

A

Apo E

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2
Q

Activates LCAT

A

Apo A-1

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3
Q

Lipoprotein lipase cofactor (activation)

A

Apo-C-2 (Apo C II)

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4
Q

Mediates chylomicron secretion and assembly

-Secretion from enterocyte to lymphatics

A

Apo-B 48

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5
Q

Binds LDL receptor, LDL particle uptake by hepatocytles

This is needed for LDL to leave liver

A

Apo- B 100

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6
Q

Secreted by intestinal epithelial cells and delivers dietary TGs to peripheral tissue

A

Chylomicrons (90%) TGs

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7
Q

Delivers hepatic TGs to peripheral tissue

Secreted by liver

A

VLDL

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8
Q

Formed in the degradation of VLDL

Delivers TGs and cholesterol to liver

A

IDL

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9
Q

Delivers hepatic cholesterol to peripheral tissues.

Formed by hepatic lipase (modification of IDL in peripheral tissues)

A

LDL

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10
Q

This molecule is taken up by receptor mediated endocytosis ( clathrin)

A

LDL

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11
Q

Which molecule mediates reverse cholesterol transport from periphery to liver?

A

HDL

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12
Q

Which molecule acts as a repository for apolipoproteins C and E?

A

HDL

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13
Q

Which molecule increase with alcohol

A

HDL

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14
Q

High Chylomicrons, TG, and cholesterol seen in blood.

Pancreatitis, hepatosplenomeglly and eruptive/puritic xanthoma

Creamy layer in supernatant

NO increase for atherosclerosis

A

Familial (AR) hyper-chylomicronemia ( type I)

Caused by lipoprotein lipase deficiency or altered apolipoprotein C 2

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15
Q

High LDL and Cholesterol seen in blood.

Causes accelerated atherosclerosis
Tendon xanthomas
Corneal arcus

MI before age 20

A

Familial hypercholesterolemia (Type 2a)

Autosomal Dominant

Absent or defective LDL receptors

KEY: MI before age 20

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16
Q

High VLDL, TG

hypertriglyceridema which can lead to pancreatitis

A

Type (4): Familial hypertriglyceridemia

Autosomal Dominant
Hepatic overproduction of VLDL

17
Q

Defect in ApoE3 + E4

A

Type 3

Familial dysbetalipoproteinemia
Liver cannot effectively remove chylomicrons and VLDL remnants from circulation

Increase in cholesterol, TG

Characterized clinically by xanthomas, premature coronary and peripheral vascular disease

18
Q

Decrease in ApoB-48 and ApoB 100

A

Abetalipoproteinemia

Autosomal Recessive
mutation in MTP gene ( microsomal transfer protein)
-decrease in chylomicrons and VLDL

Symptoms: failure to thrive, steatorrhea, Acanthocytosis (plasma membrane on red blood cell is spiky)

  • excess fat in stool
  • vitamin DEAK deficiencies– ataxia and night blindness

Tx. vit E.