L15: Cell Movement Flashcards

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1
Q

What cytoskeletal component is critical for cell migration and movement?

A

The actin cytoskeleton.

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2
Q

What is a chemoattractant?

A

A molecule that attracts cells, guiding their movement towards its higher concentration.

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3
Q

Describe the process of actin polymerisation.

A

Actin monomers add to the filament’s end, generating force and pushing the cell membrane forward.

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4
Q

What is the Arp2/3 complex?

A

A protein complex that assists in the nucleation of new actin filaments, helping the cell to organize actin for movement.

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5
Q

What role do capping proteins play in cell movement?

A

They stop actin polymerisation by binding to the filament end, regulating actin filament growth.

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6
Q

Why is actin filament recycling important in migrating cells?

A

Recycling maintains a supply of actin monomers for new polymerisation, crucial for continuous cell movement.

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7
Q

What are filopodia, and what is their function?

A

Thin, finger-like projections from a cell that help sense the environment and guide cell direction.

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8
Q

Define lamellipodia.

A

Broad, flat, actin-rich extensions at the front of the cell that drive the cell’s movement forward.

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9
Q

What are stress fibres, and what is their role in cell movement?

A

Actin-myosin bundles that generate tension within the cell, aiding in cellular contractility and movement.

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10
Q

How does the cell detach its rear to facilitate forward movement?

A

By breaking down adhesions at the back, allowing the cell body to follow the front as it migrates.

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11
Q

What are nucleation proteins, and why are they essential?

A

Nucleation proteins, such as the Arp2/3 complex, facilitate the rapid formation of new actin filaments at desired locations in the cell.

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12
Q

Explain the concept of ‘comet tails’ in cell movement studies.

A

In experiments with listeria bacteria, actin filaments form comet-like tails behind bacteria, demonstrating how actin polymerisation propels bacteria forward within cells.

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13
Q

What role does the protein ‘cofilin’ play in actin filament dynamics?

A

Cofilin binds to ADP-actin subunits, destabilizing and disassembling actin filaments, aiding in actin recycling.

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14
Q

Describe the function of profilin in actin filament turnover.

A

Profilin promotes the exchange of ADP for ATP on actin monomers, preparing them for reincorporation into new filaments.

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15
Q

What is the significance of the ATP-actin and ADP-actin forms in filament dynamics?

A

ATP-actin adds to the growing end of the filament, while ADP-actin, prone to disassembly, assists in recycling actin at the filament’s older regions.

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16
Q

How do filopodia and lamellipodia work together in cell migration?

A

Filopodia sense the environment and determine direction, while lamellipodia push the cell membrane forward, committing to movement in that direction.

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17
Q

What are focal adhesions, and why are they important for migrating cells?

A

Focal adhesions are contact points where cells attach to the substrate, anchoring the cell during migration and providing traction for forward movement.

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18
Q

How does myosin contribute to stress fibre function?

A

Myosin interacts with actin in stress fibres, generating contractile force that pulls on the cell’s cytoskeleton, aiding movement and structural integrity.

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19
Q

What is the main structural difference between filopodia and lamellipodia?

A

Filopodia consist of tight, parallel actin bundles, while lamellipodia are made of a branched, dendritic network of actin filaments.

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20
Q

Why is dynamic cytoskeletal regulation crucial for immune cell function?

A

Immune cells, such as neutrophils, rapidly change direction to pursue pathogens, requiring a flexible and responsive actin cytoskeleton.

21
Q

What is the role of adhesion turnover in cell migration?

A

Adhesion turnover allows the cell to release rear adhesions and form new ones at the front, coordinating detachment and reattachment for forward movement.

22
Q

How does actin polymerisation generate force at the cell membrane?

A

Actin monomers add to the filament, pushing the membrane outward and driving cell protrusions like filopodia and lamellipodia.

23
Q

In what way does listeria bacteria use actin for movement within host cells?

A

Listeria expresses a protein that mimics an actin-binding protein, hijacking host cell actin to form a ‘comet tail’ that propels the bacteria forward.

24
Q

What is a dendritic network in the context of actin structures?

A

A dendritic network is a branched structure formed by actin filaments, commonly found in lamellipodia, pushing the cell forward during migration.

25
Q

What are the three essential requirements for actin-based motility?

A

1) Actin filament nucleation, 2) filament capping to regulate length, and 3) recycling of actin monomers for sustained movement.

26
Q

Why is it necessary for a cell to recycle actin monomers?

A

Recycling conserves the finite amount of actin in the cell, enabling continuous filament turnover during active migration.

27
Q

Describe the concept of ‘treadmilling’ in actin dynamics.

A

Treadmilling involves simultaneous addition of actin monomers at one end of the filament and removal at the other, allowing continuous filament turnover.

28
Q

What triggers the switch from filopodia to lamellipodia formation in migrating cells?

A

Once the cell commits to a direction sensed by filopodia, it expands lamellipodia to push the cell forward in that direction.

29
Q

How does the Arp2/3 complex contribute to the formation of a dendritic network?

A

The Arp2/3 complex binds to the side of existing actin filaments, creating branch points for new filament growth, forming a dense, branched network in structures like lamellipodia.

30
Q

What is the role of nucleation in actin filament formation?

A

Nucleation is the initial step of actin filament formation, involving the assembly of actin monomers into a stable trimer to begin filament growth.

31
Q

Why is the regulation of actin filament length important in cell migration?

A

Regulating filament length through capping proteins prevents excessive filament growth, allowing cells to control the location and timing of actin polymerisation for precise movement.

32
Q

Explain the significance of actin turnover in quickly changing cellular environments.

A

Actin turnover allows cells to disassemble and reassemble actin filaments rapidly, enabling quick changes in movement direction and response to environmental cues.

33
Q

What is the role of myosin in stress fibres?

A

Myosin interacts with actin within stress fibres to generate contractile forces that pull different parts of the cell together, aiding in movement and shape maintenance.

34
Q

What structural characteristic of filopodia aids in environmental sensing?

A

Filopodia are thin, rigid, parallel bundles of actin filaments that extend from the cell, allowing it to probe and detect directional signals.

35
Q

How do cells maintain the balance of actin polymerisation and depolymerisation?

A

Cells use regulatory proteins like cofilin for depolymerisation and profilin for ATP exchange, ensuring a balanced supply of actin monomers for continuous filament turnover.

36
Q

Describe how the ‘comet tail’ phenomenon helps in studying actin dynamics.

A

The ‘comet tail’ observed in bacteria like listeria highlights how actin polymerisation at one end pushes bacteria forward, serving as a model for understanding cell motility mechanisms.

37
Q

What effect does actin filament capping have on filament dynamics?

A

Capping halts polymerisation at the filament end, stabilizing the filament’s length and allowing precise control of cell structure and movement.

38
Q

How does actin polymerisation drive membrane protrusion in migrating cells?

A

Actin monomers add to the filament’s barbed end, generating force that pushes the cell membrane outward, forming structures like filopodia and lamellipodia.

39
Q

What are focal adhesions, and how do they assist in cell migration?

A

Focal adhesions are points where cells adhere to the substrate, providing anchor points and traction as the cell moves forward.

40
Q

How does the structure of stress fibres contribute to cellular contraction?

A

Stress fibres contain actin and myosin, which interact to produce contraction, pulling parts of the cell together and generating internal tension.

41
Q

Why do cells need both filopodia and lamellipodia during migration?

A

Filopodia provide environmental sensing, while lamellipodia are broad extensions that drive forward movement, combining to guide and push the cell.

42
Q

What role does ADP-actin play in the recycling of actin filaments?

A

ADP-actin at the filament’s older end is targeted by cofilin, leading to disassembly and recycling of actin monomers for new polymerisation.

43
Q

How does actin monomer recycling support continuous cell migration?

A

Recycling supplies a steady flow of actin monomers, allowing cells to maintain filament turnover and sustain movement without exhausting resources.

44
Q

What is the function of VCA domain proteins in actin filament nucleation?

A

VCA domain proteins assist the Arp2/3 complex in recruiting actin monomers, accelerating filament nucleation and supporting rapid cell movement.

45
Q

How does the cell know where to form new actin filaments?

A

Actin-binding proteins like the Arp2/3 complex and VCA domain proteins localize to specific areas, initiating nucleation where new filaments are needed.

46
Q

What is the role of actin-binding proteins in organising different actin structures?

A

Actin-binding proteins regulate filament bundling, branching, capping, and disassembly, creating distinct structures like filopodia, lamellipodia, and stress fibres for various functions.

47
Q

How does the leading edge of a migrating cell differ from the rear?

A

The leading edge contains actin polymerisation driving forward movement, while the rear has stress fibres and focal adhesions that pull the cell body and release attachments.

48
Q

What is the relationship between actin polymerisation and cell adhesion in movement?

A

Actin polymerisation pushes the cell forward, while focal adhesions secure the cell to the substrate, working together to maintain traction and direction.