Session 5: Cytomotility Flashcards

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1
Q

What triggers cytomotility?

A

signals from the environment initiate movement
- chemical signals can be received by cell surface receptors
- environmental signals can form chemical gradients

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2
Q

What are the two different cytomotility types/migration responses?

A

chemotaxis - chemotactic cells move up gradient, toward higher concentration of attractive factor IN SOLUTION
- ex. wound fluid - WBC migrates toward the wound bc of gradient of bacterial debris solubilized into the wound fluid

haptotaxis - haptotactic cells move up gradient, toward higher amount of attractive factor BOUND TO SURFACE
- ex. epithelial cell migrating towards wound bed - cells are triggered to recover the wound bc of the gradients of depositing/attractive factors

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3
Q

List the four roles of cytoskeleton

A

cellular level “amoeboid” motility
- cell movement in response to chemotactic or haptotactic stimulus
- metastasis
- infection clearing
- wound healing

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4
Q

Describe cellular movement in response to chemotactic or haptotactic stimulus

A
  • mostly ACTIN (MF) based mechanism
  • some MTs are used to extend membrane
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5
Q

Describe metastasis through cellular motility

A

malignant cells migrate beyond tumor (spreads cancer to other areas)

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6
Q

Describe responsibility of cellular motility on infection clearing

A

WBC migration towards infection through cellular amoeboid movement to fight infection

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7
Q

How does cellular motility lead to wound healing?

A

epithelial and fibroblast migration towards wound

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8
Q

Explain treadmilling relative to movement of actin subunits

A

polymerization adds actin monomers to the + end
depolymerization removes actin monomers from the - end
result: there is net gain at the + end cell edge –> pushes membrane forward and extends stress fibers

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9
Q

Explain the actual process of microfilaments moving through the cell (PAR) - STEP 1

A

Protrusion - extension of the + end
- actin is polymerized at the + end of the membrane
- narrow (filapodia)
- flat (lamellipodia)

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10
Q

Explain the process of microfilaments moving through the cell (PAR) - STEP 2

A

Adhesion - connection to the cell
- adhesion plaque = focal contact
- stress fibers are made of MFs (connect to focal contacts)
- for the cell to properly migrate, it has to be connected to the cell to “ground it”

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11
Q

Explain the process of microfilament migration through the cell (PAR) - STEP 3

A

Retraction - release of the - end
- adhesion plaque disassembly (depolymerization)
- detaches from the substrate
- the cell must detach from the tail end in order to move forward

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12
Q

What type of structures do microfilaments have within the cell to cause intracellular movement?

A
  • transient structures
  • stable structures
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13
Q

What are transient MF structures responsible for inside the cell?

A

contractile rings - responsible for the division of daughter cells
- in cell division

vesicle movement
- actin filament with myosin 1 motor protein
- myosin motor proteins are connecting/releasing the vesicle from the surface it’s attached to to get migration

filopodia for migration

extensions for phagocytosis

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14
Q

Explain how stable microfilament structures are responsible for intracellular movement.

A

sacromeres for muscle contraction
- long term association of actin and myosin 2 motor proteins
- low phospho-titin (accessory protein) is compatible with stability of sarcomere

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15
Q

Explain the ways tubulin-based movement impacts activity within the cell

A

membrane extension
- MT positive ends at the edge of the cell are minor but important component of amoeboid movement

chromosome seperation
- coordinated polymerization at midline
- depolymerization at pole

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16
Q

What would the effect of taxol be on the mitotic spindle?

A

taxol stabilizes the polymer and prevents depolymerization –> the cell isn’t going to divide

17
Q

What type of cytoskeletal system is responsible for cilia and flagella?

A

microtubules

18
Q

What is the role of motor proteins?

A

form bridge between microtubule and organelle
- requires ATP for movement
- ONE WAY movement only
- a type of MAP (microtubule-associated protein)

19
Q

What are the two distinct types of motor proteins?

A

dyeneins - move towards cell interior (towards - end)
kinesins - move towards cell edge (towards + end)

20
Q

Explain how MTs are responsible for transport through neurons

A
  • neuron protein synthesis
  • transport thru axons and dendrites (dependent on intact microtubule: organelles or secretory vesicles)
  • two way transport (bc of kinesins and dyneins)
21
Q

What is the role of cilia and flagella?

A
  • has stable core of microtubules
  • motor proteins carry cargo along MT core
22
Q

What conditions would cilia be a good drug target for? why?

A

congestion/cystic fibrosis
- researchers found taste receptors for bitter compounds on cilia membrane –> cells exposed to bitter compounds increased Ca2+ levels and increased ciliary beating
- targeting cilia will target the bitter compounds found on cilia