ECM Flashcards

1
Q

What is the extra cellular matrix?

A

A complex network of proteins and carbohydrates that fill the spaces between cells

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2
Q

What type of components does the ECM consist of?

A

Fibrillar and non-fibrillar components

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3
Q

What does fibrillar mean?

A

Makes fibre

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4
Q

What are the two types of roles that the ECM plays in the cell?

A

an architectural role (influencing mechanical stability) and an instructional role (influences cell behaviour)

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5
Q

What three things is the ECM essential for?

A

Development, tissue function and organogenesis

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6
Q

What are they key functions of the ECM?

A
  1. Physical support
  2. Determines mechanical and physicochemical properties of tissue
  3. Influences the growth, adhesion and differentiation status of the cells and tissues
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7
Q

What type of tissue is particularly rich in extra cellular matrix?

A

Connective tissue

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8
Q

What are the three main components of the extra cellular matrix?

A

Collagens
Multi-adhesive glycoproteins
Proteoglycans

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9
Q

What is found in the basement membrane?

A

Type IV
Laminins
Perlecan

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10
Q

How can connective tissues have such varied properties?

A

the different types and arrangements of collagen, with the presence of different ECM components

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11
Q

What properties do connective tissues in the tendon and skin have?

A

Tough and flexible

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12
Q

What properties do connective tissues in bone have?

A

Hard and dense

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13
Q

What properties do connective tissues in the cartilage have?

A

Resilient and shock absorbing

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14
Q

What cell produces collagen

A

fibroblasts

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15
Q

What is connective tissue made up of?

A

Extracellular matrix and component cells

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16
Q

What are three proteoglycans?

A

Aggrecan, versican and decorin

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17
Q

What type of protein is collagen?

A

Fibrous

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18
Q

How many different collagen types exist in humans?

A

28

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19
Q

What structure does collagen form?

A

Triple helix

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20
Q

What is meant y a homotrimer?

A

When there is only one chain type

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21
Q

Which types of collagen are homotrimers?

A

Type II and III

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22
Q

What are the compositions of type II and type III collagen?

A

[a1(II)]3 and [a1(III)]3

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23
Q

What is meant by a heterotrimer?

A

When the chains arise from 2 genes

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24
Q

What type of collagen is a heterotrimer?

A

Type 1 Collagen

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25
What is the composition of type 1 collagen?
[a1(I)]2 [a2(1)]
26
What is commonly the x and y in the glycine-x-y-repeat?
``` X = proline Y = hydroxyproline ```
27
Which amino acid occupies every third position in collagen proteins?
Glycine
28
why is glycine heavily involved in the structure of collagen?
Glycine is the only amino acid which is small enough to occupy the interior of the chain
29
What provides tensile strength and stability in collagen?
Intermolecular and intramolecular cross links
30
When does cross linking in collagen take place?
Only after the collagen has been secreted
31
What is an essential post- translational modification which contributes to interchain hydrogen bond formation?
The hydroxylation of proline and lysine
32
What enzymes are needed for the hydroxylation of proline and lysine?
Prolyl hydroxylase and Lysyl hydroxylase
33
What do Prolyl hydroxylase and Lysyl hydroxylase requires as a co-factor?
Vitamin C
34
What happens to collagen when you have vitamin C deficiency?
The collagen is underhydroxylated
35
When does the cross linking of collagen occur?
After the fibril formation
36
which collagens are fibril associated?
type 9 and 10
37
What do fibril associated collagens do?
They regulate the organisation of collagen fibrils in the tissues
38
What are the symptoms of Ehlers-Danlos syndrome?
Stretchy skin and loose joints due to mutations affecting collagen production in connective tissue
39
How is the tensile strength of collegan established?
The fibres are held in parallel bundles which resist the tensile force in one direction
40
What are collagen alpha chains synthesized from?
Longer precursors called pro-alpha chains
41
what is cleaved from procollagen to make collagen?
N-terminal propetide and C-terminal propeptide
42
Where is type 4 collagen found?
In all basement membranes
43
What type of network does type 4 collagen form?
A sheet-like network
44
What happens to the N and C terminus in type 4 collagen?
It remains intact
45
What is another name for basement membranes?
Basal lamina
46
What is the basement membrane?
A thin, flexible mat of extra-cellular matrix which the epithelial cell sheet sits on top of
47
What structures are surrounded by basement membrane?
muscle, peripheral nerve and fat cells
48
What do basement membranes form a part of the kidney?
They form a key part of the filtration unit as the glomerular basement membrane
49
What is diabetes nephropathy?
Disorder where there is an accumulation of ECM leading to highly thickened basement membrane
50
What is Alport Syndrome?
Where mutations in collage IV result in abnormally laminated Glomerular basement membrane which is associated with progressive loss of kidney function and hearing loss
51
What helps to limit the extent of elastic fibres stretching?
The elastic fibres are interwoven with collagen
52
What do elastic fibres consist of?
A core made up of elastin protein, surrounded by microfibrils which are rich in the protein fibrillin
53
What amino acid side chains are covalently cross linked in elastin?
Lysine
54
Describe the structure of elastin fibres
Elastin consists of two types of segments that alternate along the polypeptide chain: hydrophobic regions and a alpha-helical region that is rich in lysine and alanine - many of these lysin side chains are covalently crosslinked
55
Where is fibrillin found?
In the microfibrils which surround the elastin core
56
Mutations in fibrillin-1 are associated with what syndrome?
Marfans Syndrome
57
What are patients with Marfans syndrome pre-disposed to?
Aortic ruptures
58
How are ECM proteins able to multi-function?
They have a modular structure
59
What is meant by multi-adhesive modular proteins?
The proteins can bind various matrix components and cell-surface receptors
60
What is the shape of the laminin molecule?
A cross shape due to the presence of three chains - alpha, beta and gamma
61
Are laminins large or small proteins?
Large
62
Which surface cell receptors can laminins interact with?
Integrins and dystroglycans
63
What mutation of laminin results in muscular dystrophy?
absence of the alpha 2 chain in laminin 2
64
What are some symptoms of congenital muscular dystrophy?
hypotonia, generalised muscle weakness and deformities of the joint
65
What are the two forms which fibronectins can exist as?
Insoluble fibrillar matrix or a soluble plasma protein
66
How are different forms of fibronectins formed?
Alternate splicing of mRNAs
67
What do fibronectins do?
play an important role in regulating surface adhesion and migration in a variety of processes, notably embryogenesis and tissue repair
68
What is a proteoglycan?
core proteins which are covalently bonded to one or more glycosaminoglycan chains
69
What proteoglycan is considered small and leucine rich?
Decorin
70
What is the name of a cell surface proteoglycan?
Syndecans
71
What is a GAG chain?
Glycosaminoglycan chain
72
What makes up a GAG chain?
Repeating disaccharide units with one of the two sugars being an amino sugar
73
What is an amino sugar?
A sugar in which one of the hydroxyl group is replaced with a amine group
74
What has to happen to the GAG chain in order for it to carry a high negative charge?
Has to be sulfated or carboxylated
75
What effect does the high negative charge of the GAG chain result in?
it attracts clouds of cations, including Na+, which therefore pulls water into the ECM through osmosis and the presence of a concentration gradient
76
why does cartilage have a high tensile strength?
Catilage has a ECM with alot of collagen and GAG chains trapped in the meshwork, so the balance of swelling pressure is negated by the tension in the collagen fibres
77
What are the four groups of GAG chains?
Hyaluronan Chondroitin sulfate Heparan sulfate Keratan sulfate
78
How is hyaluronan produced?
It is spun out directly from an enzyme embedded in the plasma membrane
79
How id hyaluronan distinct from other GAG chains?
It is simply a carbohydrate chain without a core protein
80
Why can hyaluranan chains occupy large volumes?
Because it can undergo a very high degree of polymerisation, which creates very large molecules
81
What is the role of hyaluronan in joints?
Protects the cartilaginous surfaces from damage
82
What is a major constituent of the cartilage ECM?
Aggrecan
83
Aggrecan is highly sulphated What effect does this have?
Increases their negative charge which attracts cations that are osmotically active - leads to large amounts of water being retained by the negatively charged environment
84
what is osteoarthiritis?
an erosive disease resulting in excessive ECM degradation
85
What is lost with osteoarthiritis?
The cushioning properties of cartilage over the end of bones
86
What leads to a loss of aggrecan fragments to the synovial fluid?
The cleavage of aggrecan by aggrecanases and metalloproteinases - this increases with age
87
How do fibrotic diseases arise?
They are as a result of excessive production of fibrous connective tissue
88
How is aggrecan perfectly suited to resist compressive forces in cartilage matrix?
Under compressive load, water is given up but is regained once the load is reduced