10. Cell Motility Flashcards

1
Q

What is the function of focal adhesions in cell motility?

A

Act as “hooks” for cells onto surfaces so that they can move forwards in a collective manner

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2
Q

How are focal adhesions formed?

A

Integrin dimer receptors act as hooks, which attach cytoskeletal components via docking sites in their short cytoplasmic domains

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3
Q

Which cytoskeletal component is used in focal adhesions?

A

Filamentous actin = like “muscles of cell”

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4
Q

Recall the 3 main peripheral actin structures involved in motility

A

Lamellipodia
Filopodium
Stress fibres

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5
Q

Describe the structure and function of lamellipodia

A

Structure: stretchy membrane
Function: expands and contracts to move cell forwards

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6
Q

Describe the structure and function of folipodia

A

Structure: Finger-like protrusions
Function: sensory = environmental exploratory

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7
Q

Recall the actin arrangement in lamellipodia

A

Mesh/net-like

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8
Q

Recall the actin arrangement in filopodia

A

Parallel filaments

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9
Q

Recall the actin arrangement in stress fibres

A

Anti-parallel (for contraction)

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10
Q

Distinguish G-actin and F-actin

A
G-actin = monomer
F-actin = polymer
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11
Q

Recall the 6 actin-driven processes that need to be controlled

A
  1. Remodelling
  2. Elongation
  3. Capping
  4. Severing
  5. Cross-linking/ bundling
  6. Branching
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12
Q

Distinguish hapoptatic and chemotactic movement

A
Hapoptatic = aimless non-directional cell movement
Chemotactic = purposeful, polar movement
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13
Q

Which family of proteins are involved in regulation of actin remodelling

A

Arp

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14
Q

What is the limiting step in actin remodelling reactions

A

Trimerisation of monomer before it can polymerise

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15
Q

Summarise the control of actin filament elongation

A
  1. Promoted by prolifin which binds to G-actin to transport it onto the end of new filaments
  2. Inhibited by thymosin, which competes with prolifin for actin-binding
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16
Q

Give examples of 2 proteins that bind to the positive end of actin

A

CapZ

Severin

17
Q

Give examples of 2 proteins that bind to the negative end of actin

A

Tropomodulin

Arp

18
Q

What is the function of severing actin filaments?

A

Allows growth/ shrinking of filaments to be sped up

19
Q

Recall the 3 possible fates of severed actin filaments

A
  1. Barbed ends capped
  2. Annealed
  3. Added to a new strand
20
Q

Recall 2 proteins involved in control of actin cross-linking and the resulting actin structure

A
  1. Alpha-actinin –> cross linking of parallel strands = like a ladder
    2, Filamin –> V-shaped actin filament
21
Q

Which protein family is involved in controlling actin branching?

A

Arp complex

22
Q

Recall the family of proteins involved in signalling the development of each different actin structure in locomotion, and which individual protein drives development of each structure

A

Rho (Subfamily of Ras)
Lamellipodia = Rac
Filopodia = CDC42
Stress fibres = Rho

23
Q

Summarise the process of de-differentiation that leads to production of a benign tumour

A
  1. Disassembly of cell-cell contacts

2. Loss of polarity

24
Q

Summarise the processes that lead to progression of a benign tumour to a malignancy

A

Invasion of BM
Increased motility
Cleavage of ECM proteins

25
Q

Summarise the process of metastasis

A

• Metastatic cells become mobile mesenchyme-type cells + enter bloodstream. When they reach new organ = lose their mesenchymal characteristics to form new tumour

26
Q

What are the 2 broad methods of cell migration? Give 2 examples of mechanisms for each of these

A
  1. Single-cell (ameboid movement, mesenchymal)

2. Collective movement (clusters, multicellular strands)

27
Q

Give an example of a cancer type that shows a preference for amyboid movement

A

Leukaemia

Lymphoma

28
Q

Give an example of a cancer type that shows a preference for collective multicellular strand movement

A

Glioblastoma

29
Q

What genetic change is often seen in tumours that have lost contact-inhibition?

A

Upregulation of cytoskeletal regulator and motility machinery genes