Cell death Flashcards

1
Q

How do cells die?

A

Necrosis:
- Mass death of cells at same time
- Caused by external signal damaging the cell
- Generally associated with physical damage e.g. burns and cuts
Apoptosis
- Very controlled singular at a time cell death
- Programmed
- 50 billion cells per day
- Can be caused by very precise external signals but mainly by internal signals
More than one of these can be involved in the death of a cell, isn’t exclusive

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2
Q

When does necrosis occur?

A

Physical damage
- Trauma e.g. cuts and burns
- Extreme temperatures e.g. frostbite
Toxins
- External e.g. snake venom
- Internal e.g. bacterial toxins
Acute hypoxia/ischaemia e.g. stroke
Cellular death then causes cell insides to spill out into surrounding area, this then causes very sever inflammatory response in nearby cells which when spread becomes dangerous

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3
Q

When does apoptosis occur

A

Occurs everywhere and is a key part of keeping the body functioning
Physiological situations:
- Tissue size maintenance
- Developmental cell loss - growth factors
- Removal of immune cells
- Hormone - dependent involution
- Inappropriate interactions - Anoikis (tells cells when they are in the wrong place and interacting with the wrong cells)
Pathological situations:
- DNA damage e.g. radiation, oxidative stress
- Virally infected cells

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4
Q

Characteristics of necrosis

A

Reversible:
- Membrane integrity compromised
- Organelle and cell swelling
Irreversible:
- Increased intracellular calcium
- Autolysis
- Cell bursting (cell lysis)
- Elicits an inflammatory response

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5
Q

Characteristics of apoptosis

A

Shrinkage
Nuclear breakdown
Apoptotic bodies
Phagocytosis
No inflammatory response (because there is no loss of membrane integrity)
Requires energy
Controlled cell death
Relationship with autophagy

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6
Q

Necrosis or apoptosis - brain ischaemia

A

Both may be involved in the death of cells during an event
Cells in middle die through necrosis
Cells at edge die through apoptosis
This restricts spread of cell death

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7
Q

Developmental apoptosis

A

C. elegans
Nematode worm
1 mm long with ~ 110 cells
131 die in development
Metamorphosis e.g. tadpole - frog
- Surge in thyroid hormone in the blood initiate apoptosis in tail cells
Digit formation in mice:
- Apoptosis is initiated through release of local signal proteins
Neuronal connections are refined by the competition for survival factors
Not enough survival factor = apoptosis

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8
Q

Ced genes

A

C-elegans provide good model for studying apoptotic pathways
Ced genes involved from recognition of apoptotic signal to engulfment of apoptotic cell by phagocytes
Manny c.elegans genes are conserved in mammals:
- EGL-1 -> BH3-only proteins
- Ced 9 -> Bcl-2
- Ced 4 -> APAF-1
- Ced 3 (apoptotic initiator) -> caspases
EGL-1 inhibits Ced 9 which inhibits Ced4 which promotes Ced3 which leads to death
Pro and anti apoptotic genes
- Decreases Ced 3 or 4 gives excess adult cells
- Decrease Ced 9 gives massive cell death

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9
Q

Caspases

A

The executioners of cell death = essential for apoptosis
C = cysteine at their active site
asp = aspartic acids are the cleavage site in target proteins
Irreversible pathway
10+ ced-3 homologues
Irreversible once started

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10
Q

Initiator and executioner caspases

A

Initiator caspases:
- Activated by apoptotic signals
- Activate executioner caspases
Executioner caspases:
- cleave >1000 proteins
Amplifying proteolytic cascade:
- one initiator caspase can activate multiple executioner caspases
Active caspase will then go on to cleave its targets of substrates

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11
Q

Some caspase targets

A

Causes breakdown of nucleus structure, including nuclear lamina through cleavage of nuclear lamins
Prevents DNA repair by cleaving DNA repair enzymes PARP (Poly ADP-ribose polymerase)
Cause cytoskeletal changes, e.g. the breakdown of actin, by cleaving cytoskeletal proteins like Gelsolin

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12
Q

There are two main ways of initiating apoptosis

A

Extrinsic pathway
Intrinsic pathway

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13
Q

Extrinsic pathway

A

Tumour necrosis factor family
6 related receptors - the death receptors
Indirectly (via the DISC activate initiator caspases
E.g.
- Apoptotic signal = Fas ligand on killer lymphocyte
- Caspase-8 = initiator caspase
- DISC = death-induced signalling complex
Fas ligand is what causes the extrinsic pathway of apoptosis to be activated

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14
Q

Intrinsic pathway

A

Triggered by:
- Stress signals e.g. DNA damage
- Developmental signals
Example
- Cytochrome C release from mitochondria
- Adaptor protein = Apaf-1 = apoptotic protease activating factor
- Caspase-9 = initiator caspase
Balance between pro and anti apoptotic factors known as Bcl2 family proteins
- EGL-1 homologue Bh3-only protein = pro-apoptotic
- Ced9 homologue Bcl2 protein = anti-apoptotic

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15
Q

Apoptosis pathways - simply summary

A

Activated by cell death inducing stimuli
Caspases cleave proteins involved in:
- Inhibiting apoptosis
- DNA repair
- Cell cycle
- nuclear structure

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16
Q

Summary

A

Cells defences may be overcome rapidly, leading to necrosis
Cells have a mechanism for a clean death - apoptosis
Apoptosis is widely used during development, maintenance of tissue size and to prevent pathological conditions
Cells are on a tightrope due to pro- and anti-apoptotic factors