Collagen/Elastin Flashcards

1
Q

Which is the main structural protein of the extracellular matrix?

A

Collagen

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2
Q

Collagen type 1 can be found in

A

Bone, skin, tendons

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3
Q

Collagen type 2 can be found in

A

Cartilage

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4
Q

Collagen type 3 can be found in

A

Blood vessels, granulation tissue, uterus

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5
Q

Collagen type 4 can be found in

A

Basement Membrane

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6
Q

Collagen structure

A

Three alpha chains linked by disulfide bonds (also hydrogen bonds)

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7
Q

Steps in Collagen synthesis (6 steps)

A
  1. Synthesis of individual alpha chains
  2. Hydroxylation of Proline and Lysine
  3. Glycosilation of hydroxyproline = Procollagen
  4. Exocytosis of procollagen
  5. Cleavage of terminal regions
  6. Cross-linking between collagen molecules
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8
Q

Which step of collagen synthesis needs Vit C?

A

Hydroxilation of proline and lysine

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9
Q

Hydroxilation of proline and lysine needs ____________

A

Vitamin C

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10
Q

Osteogenesis imperfecta affects which type of Collagen?

A

Type 1

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11
Q

Clinical features of Osteogenesis imperfecta

A

Bone fragility + Blue sclera + Dental problem/Hearing loss

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12
Q

Osteogenesis imperfecta inheritance pattern

A

Autosomal Dominant

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13
Q

Ehlers Danlos affects which type of Collagen

A

Type 3 (Also Type 5)

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14
Q

Ehlers Danhlos Clinical features

A

Hypermobile joints and Hyperextensible skin
Type 5: More vascular compromise

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15
Q

Merkes Syndrome is caused by

A

Poor copper absorption = Decreased collagen synthesis

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16
Q

Merkes Syndrome clinical features

A

Brittle hair + Cognitive impairment

17
Q

What is elastin?

A

Large and very stretchy protein commonly found in connective tissue

18
Q

Sites where you can find Elastin

A

Skin, blood vessels, lungs and Ligament flava

19
Q

What action does Alpa-1- Antitrypsin do?

A

Increases elastase activity = Decrease elastin

20
Q

Syndrome characterized by defective fibrillin?

A

Marfan Syndrome

21
Q

Patient with Marfanoid Habitus + Pectus carinatum + Aortic incompetence. Diagnosis

A

Marfan Syndrome

22
Q

Marfan syndrome pathogenesis:

A

Defective fibrillin (Decreased production of sheath around elastin)

23
Q

Lens abnormality associated to Marfan Syndrome

A

Superotemporal/Temporal Lens subluxation

24
Q

Marfan Syndrome inheritance pattern

A

Autosomal dominant