Describe the importance of the Bcl-2 family of proteins and the role of mitochondria in the apoptotic pathway
Explain the function and activation mechanisms of the caspases, the apoptosis executioners
Demonstrate an understanding of the role of trophic factors in cell survival, and how withdrawal of trophic factors induces apoptosis
Explain how death receptors, such as Fas, induce apoptosis
Give examples of the role of apoptosis in health and disease
Cytotoxic T cells cause killing, NK cells - regulated apoptosis
P53 pathway activation (elimination of pre-malignant cells)
Tissue homeostasis: small bowel crypts, skin keratinocytes (between digits on hands/feet), thymus (non responsive and self reactive T cells)
Outer lens of eye
During development- in particular metamorphosis
Necrosis
Cell death following injury and results in inflammatory response
Cell undergoes injury, contents leak out
Apoptosis
Controlled non-inflammatory event
No injury, no content leakage
Active signal- cell fragmentation and form apoptotic bodies, engulfed by phagosome and taken to lysosome
Slide 5
Intracellular Proteolytic Caspase Cascade
Initiator caspases (8, 9) dimerize and become active
Initiator caspases cleave executioner caspase (3,6,7) subunits-> activate executioners
Executioners cleave cellular substrates and cell undergoes apoptosis
Once executioners active, only way to stop apoptosis is to digest caspase, happens at end of apoptosis
Caspases:
Activators/initiators (8,9,19,2)
Executioners/effectors (3,6,7)
Inflammatory (unrelated to apoptosis)
Activated by dimerisation (initatiors) or proteolysis (effectors)- executioners have small and large subunits that need to be cleaved
One can activate another (positive feedback)
CAD= Caspase Activated DNase
In healthy cells- endonuclease CAD is bound to inhibitor - iCAD
Apoptosis- Induces iCAD cleavage by executioner caspase, release active DNase which cleaves DNA between nucleosomes
One caspase activate many other caspases, activate many others and cleave multiple susbtrates
Capases cleave nuclear proteins (lamins) and cytoskeletal proteins (actin)
Caspases cleave and activate gelsolin which induces actin severing
Result= nuclear fragmentation, disruption of cytoskeleton, membrane blebbing, cell fragmentation
Extrinsic:
Cell receives explicit signal from extracellular environment to initiate apoptosis- eg death ligand expressed on another cell
Intrinsic:
Normally involves release of cytochrome c- induced by stress, damage, developmental cues
Slide 10
Extrinsic Induced by Death Receptors
Death receptors= cell surface receptors that initiate apoptosis following ligand binding
Receptors are part of TNF family:
Fas (CD95/APO-1)
TNF-R1 (tumour necrosis factor receptor 1)
Ligands:
FasL(CD95L)
TNF-a, TRAIL (TNF-related apoptosis inducing factor)
Slide 11
Extrinsic Induced by Death Receptors
Death receptors interact with adaptor proteins through mutual death domains (DDs)- Fas and TNRF1 have extracellular DDs
FasL binds Fas death receptor
Fas interacts with an adaptor protein FADD (via Fas-associated DD)
FADD complexes with procaspase-8 via DED domain (Death Effector Domain)-> activated caspase 8 that can cleave executioner
Forms Death Inducing Signal Complex (DISC)
Infected cell presents a virus peptide on its cell surface with MHC-I
MHC-I:peptide interacts with TCR on cytotoxic T cell
T cell has Fas ligand that binds Fas receptor on target cell-> sends apoptotic signal
CD4 T cells express Fas, but HIV-infected cells also express high levels of FasL
Induces non-infected CD4 T cell to commit suicide
Results in failure of immune response
Infected HIV cell survives as high FasL prevents interaction with own Fas
Slide 15
Intrinsic Apoptosis
1. Apoptotic stimulus causes cytochrome c release from mitochondria
2. Cytochrome c binds Apaf1 (Apoptotic protease activating factor)
3. CARD domain of Apaf1 associates with other CARD domains and forms apoptosome (CAspase Recruitment Domains)
4. Caspase 9 (initiator) recruited via its CARD domain and is activated-> cleaves and activates executioner
Bcl-2 family contains both pro- and anti- apoptotic members
Bcl-2 is anti-apoptotic
Healthy cells maintain balance of pro and anti apoptotic proteins
Relative expression of anti/pro can promote or repress apoptosis
All proteins regulated by TFs
BH= Bcl-2 homology domain
BH3- only proteases that promote apoptosis by inhibiting anti-apoptotic Bcl-2 family proteins
Pro-apoptotic proteins (Bax/Bak) in mitochondrial membrane
Bcl-2 in membrane in dimer with Bcl-xL (antiapoptotic complex) can inhibit Bax and Bak
BH3 only BH domain protein that can bind and inhibit Bcl-2 and initiate apoptosis
Activates Bax in membrane and allows release of cytochrome c
Trophic factors- inducing differentiation/survival eg NGF (nerve) and EGF (epidermal)
Absence of trophic factor:
No signalling via PI3 kinase/Akt pathway
Bad (BH3) binds to Bcl2(anti)-> activates Bak(pro), release cytochrome c
Presence and binding to trophic factor:
Receptor activated, stimulate PI-3 kinase phosphorylates and activate Akt(PKB)-> phsophorylates Bad
Phospho-Bad forms complex with 14-3-3 protein (sequesters Bad from mitochondria membrane)
Prevents Bad(BH3)from interacting with Bcl-2(anti), no activation of Bax(pro), no cyt c release
Survival