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Apoptosis - Programmed Cell Death

The document discusses apoptosis (programmed cell death) and compares it to necrosis. Apoptosis is an actively regulated process where cells play an active role in their own death. It occurs through signaling pathways and involves condensation of the cell and fragmentation into membrane-bound vesicles. This contained process prevents intracellular contents from leaking out and causing inflammation like in necrosis. The document outlines various intrinsic and extrinsic triggers of apoptosis and the roles of the pathways, caspases, and other cellular components involved in the apoptotic process.

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44 views16 pages

Apoptosis - Programmed Cell Death

The document discusses apoptosis (programmed cell death) and compares it to necrosis. Apoptosis is an actively regulated process where cells play an active role in their own death. It occurs through signaling pathways and involves condensation of the cell and fragmentation into membrane-bound vesicles. This contained process prevents intracellular contents from leaking out and causing inflammation like in necrosis. The document outlines various intrinsic and extrinsic triggers of apoptosis and the roles of the pathways, caspases, and other cellular components involved in the apoptotic process.

Uploaded by

dvdmega
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PPT, PDF, TXT or read online on Scribd
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Apoptosis Programmed Cell Death

(True/False) In adult tissues cell death exactly balances cell division In apoptosis the cell destroys itself from within and avoids leakage of the cell contents into the extracellular space. Why do you think that this occurs via a different mechanism than in necrosis? What are some signals that indicate to a cell that apoptosis needs to occur? Where do these signals come from? What are some cellular components involved in the apoptotic pathway? What is the difference between a mitogen, a growth factor, and a survival factor? In what phase of the cell cycle do cells exit to undergo apoptosis? What effects do telomeres and telomerase have on cell aging and death? If you could turn on telomerase activity in all of our cells, would it prevent aging? Do the following types of cells exist in humans?
Cells that do not grow and do not divide Cells that grow, but do not divide Cells that divide, but do not grow Cells that grow and divide

Death by Injury vs. Death by Suicide

(Necrosis vs. Apoptosis)

Necrosis
Trauma (toxic chemicals, mechanical injury, heat, hypoxia)
Loss of ability to regulate internal environment Ca2+ influx accompanied by swelling Alteration of protein activity

calpain
cathepsin caspase Production of toxic compounds (activation of cyclooxygenases) arachadonic acid prostaglandins

eicosanoids

Inflammation

Apoptosis Programmed Cell Death


Why? Developmental Protective (destroy cells that are a threat) infected with virus turn off immune response DNA damaged cells cancer

What makes a cell commit suicide?


withdrawal of positive signals (growth factors, Il-2) receipt of negative signals (increased levels of oxidants, DNA damage via X-ray or UV light, chemotherapeutic drugs, accumulation of improperly folded proteins, death activators such as: TNF-a, TNF-b, Fas/FasL)

Steps in apoptosis:

The actual steps in cell death require:

the decision to activate the pathway; the actual "suicide" of the cell; engulfment of the cell remains by specialized immune cells called phagocytes; degradation of engulfed cell. condensing of the cell nucleus and breaking it into pieces condensing and fragmenting of cytoplasm into membrane bound apoptotic bodies; breaking chromosomes into fragments containing multiple number of nucleosomes (a nucleosome ladder) Intrinsic or mitochondrial pathway Extrinsic or death receptor pathway

Apoptosis Triggered via Two Pathways

Extrinsic or Death Receptor Pathway

Binding of Fas by FasL induces recruitment of FADD to the cytoplasmic tail of Fas The opposite end of FADD contains a death effector domain (hatched boxes); recruitment of either procaspase-8 or c-FLIP Caspase-8 can cleave Bid truncated Bid (tBid) can inactivate Bcl-2 in the mitochondrial membrane. This allows the escape of cytochrome c, which clusters with Apaf-1 and caspase-9 in the presence of dATP to activate caspase-9. Smac/DIABLO is also released from the mitochondria and inactivates inhibitors of apoptosis (IAPs). breakdown of several cytoskeletal proteins and degradation of the inhibitor of caspase-activated DNase (ICAD).

Apoptosis is involved in

Cancer ( via HPV, Epstein bar virus; melanoma)


regulation of the immune system, AIDS, organ transplants

Melanoma (the most dangerous type of skin cancer) cells avoid apoptosis by inhibiting the expression of the gene encoding Apaf-1.

AIDS induced apoptosis

Superantigens are molecules which short-circuit the immune system, resulting in massive activation of T-cells rather than the usual, carefully controlled response to foreign antigens. The over-response of the immune system produced results in autoimmunity, as rare clones of T-cells which recognize self antigens are activated, and immune suppression, as the activated cells subsequently die or are killed by other activated T-cells. It is possible that such superantigens might also induce apoptosis

ORGAN TRANSPLANTS

Anterior chamber of the eye and testes fail to elicit an immune response because these cells produce lots of FasL, so kill immune cells when they enter these sites. Possible therapy by inducing production of FasL in other tissues lowering need for immune rejection drugs

Cytoplasm shrinks due to cleavage of nuclear lamins and actin Chromatin is broken down as nucleus condenses (often horseshoe shaped Cells shrink making an easy meal for phagocytes Cells undergo plasma membrane changes move phosphatidylserine from inner to outer leaflet of the membrane; attracts macrophages

video Jazzy video

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