ECM 1.16-1.18 Flashcards

1
Q

The ECM is the defining feature of what tissue type?

A

Connective tissue

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2
Q

What are GAGs?

A

Heteropolymer chains containing repeating disaccharide units of an amino sugar and uronic acid.

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3
Q

What are two examples of amino sugars? Examples of uronic acid?

A

N-acetylglucosamine, N-acetylgalactosamine.

Glucaronic and Iduronic acid

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4
Q

What are the major structural polysaccharides of ECM, CT, and Outer cell membrane surfaces?

A

GAGs

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5
Q

Why are GAGs highly negatively charged and easily attract water?

A

Because they contain sulfate and carboxyl groups

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6
Q

What does the accumulation of various GAGs (due to enzyme deficiencies) result in?

A

Several syndromic diseases such as Hunter’s and Hurler’s diseases.

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7
Q

Which two GAGs most frequently accumulate two cause mucopolysaccharide storage diseases?

A

Heparan sulfate and Dermatan sulfate

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8
Q

What is the most abundant GAG?

A

Chondroitin sulfate

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9
Q

Which GAG does not form a proteoglycan and does not contain sulfur?

A

Hyaluronic Acid

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10
Q

Which GAG is found in basement membranes?

A

Heparan sulfate

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11
Q

Which GAG is highly sulfated and acts as an anticoagulant?

A

Heparin

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12
Q

What are Proteoglycans (PGs)?

A

Complex carbs that have a central protein molecule to which many GAGs are attached in a radial (brushlike) pattern.

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13
Q

Which trisaccharide is involved in the linkage of GAGs to the central protein of a PG?

A

2 galactose + 1 xylose (if glucuronic acid is accounted for then it may be considered tetrasaccharide)

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14
Q

What is the central protein of a PG rich in?

A

serine and threonine

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15
Q

Where are PGs located mostly?

A

in the ECM

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16
Q

What are PG Aggregates?

A

PGs joined to a long hyaluronate molecule (not a protein core, though looks like it)

17
Q

Which GAG acts as a biological shock absorber and can be found in synovial fluid and vitreous fluid?

A

Hyaluronic acid, which does not form a PG, but has many PGs linked to it to form an aggregate

18
Q

What are the three classes of PGs?

A

Small leucine-rich proteoglycans (SLRPs).
Modular proteoglycans
Cell-surface proteoglycans

19
Q

What is required for PG degradation?

A

3 exoglycosidases
4 sulfatases
1 acetyl transferase
Removal of monosaccharides

20
Q

What is it about the conformation of PG that makes it susceptible to extracellular proteases?

A

Its linear conformation

21
Q

What is the form and function of the four extracellular matrix proteins?

A

Structure is achieved by collagen and elastin.

Adhesion is achieved by fibronectin and laminin

22
Q

What are the major functions of collagen?

A

Provides tensile strength, regulates cell adhesion, support chemotaxis and migration and directs tissue development.

23
Q

Which cells synthesize and secrete collagen?

A

Fibroblasts

24
Q

How are fibroblasts able to organize collagen fibrils into sheets and cables?

A

By exerting tension of matrix

25
Q

What are collagen proteins rich in?

A

Glycine, Proline, Hydroxyproline and Hydroxylysine