#19 Apoptosis Chapter 9 · phosphorylation is required for its apoptosis-inhibitory effect. !...
Transcript of #19 Apoptosis Chapter 9 · phosphorylation is required for its apoptosis-inhibitory effect. !...
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Cell
Death stimulation or Stress
Survival Death
Why cells decide to die? -‐ Stress, harmful, not needed -‐ Completed its life span
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Functions of PCD during Development
Fuchs and Steller. Cell Volume 147, Issue 4 2011 742 -‐ 758
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Cell Death
Controlled cell death Uncontrolled cell death
Physiological cell death or Necrotic cell death (?) Programmed cell death (Type III)
Autophagic cell death Apoptotic cell death (Type II) (Type I)
Caspase-‐independent Caspase-‐dependent
Extrinsic pathway Intrinsic pathway (Death receptor-‐mediated)
Types of Cell Death
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Fink and Cookson, Infect Immun. 2005
Types of Cell Death
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Evolutionary Conservation of the Core Apoptotic Machinery
Yaron Fuchs , Hermann Steller Cell Volume 147, Issue 4 2011 742 -‐ 758
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What is the difference between key cell death mechanisms
Apoptosis Autophagy Necrosis !-‐Genetically programmed Genetically programmed Not (?) genetically -‐Extra and intracellular Extra and intracellular Acute injury (?) (Extra) -‐Cell shrinkage Autophagic vacuoles Cytoplasm swelling -‐Blebbing Blebbing Disruption of Memb -‐Organelle intact Sequesteration Disruption -‐Chromatin condensation Partial condensation Non-‐condensed -‐DNA fragmentation (laddering) No laddering No laddering -‐Phagocytosis with Phagocytosis with Release of intracellular no inflammation no inflammation contents & inflammation -‐Caspase-‐dependent Caspase-‐independent Caspase-‐independent !
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! What is Apoptosis? -‐ A predominant form of cell death -‐ A sequence of events involving various class of proteins -‐ Genetically programmed and evolutionary conserved
Hallmarks of Apoptosis
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!-‐ Intact death program is required for successful embryonic development and maintenance of normal tissue homeostasis !-‐Insufficient or evasion of apoptosis manifest as: -‐ Cancer -‐ Autoimmunity (proliferation of immune system cells that recognize and attack self antigens) -‐ Viral infections (removal of virally infected cells by apoptosis) !-‐While accelerated cell death is related to: -‐ Neurodegenerative diseases -‐ Immunodeficiency, infertility -‐ Hematologic diseases
Why should we study apoptosis?
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Major Players in Apoptosis !!!! -‐Bcl-‐2 family proteins -‐Antiapoptotic -‐Proapoptotic multi-‐domain proteins -‐Proapoptotic BH3-‐only domain protein !! -‐Caspases -‐Initiator caspases -‐Executioner caspases
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Bcl-‐2 family proteins
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BH3-‐only proteins sense signals and galvanize action
Bcl-‐2 family proteins
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Bcl-‐2 family proteins-‐mediated apoptosis
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BAD: Phosphorylation sequesters it in the cytosol
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Bcl-‐2 family proteins-‐mediated apoptosis
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*Bcl-2 must change conformation (or be ‘activated’) on the mitochondria to inhibit Bax (Dglugosz PJ, EMBO J. 25, 2287, 2006). !*Bcl-2 and Bcl-xL (and other prosurvival members) are the guardians of the mitochondria: they are inactivated when BH3-only proteins juxtapose their BH3 domain to Bcl-2 (protein-protein interaction).. !*These proteins are transcribed into multiple splice variants. !*Bcl-2 is phosphorylated by many apoptotic stimuli. Phosphorylation of Bcl-2 within the flexible loop generally inhibits its anti-apoptotic activity. But it has also been reported that phosphorylation is required for its apoptosis-inhibitory effect. !*Bcl-2 and Bcl-xL can also be cleaved by caspases during apoptosis. Cleaved proteins turns themselves into apoptotic killers. !*Bcl-xL may undergo deamidation: deamidation of Asn imparts susceptibility to apoptosis by disrupting the ability of Bcl-xL to block the proapoptotic activity of BH3-only proteins. ! D. Tang
Regulation of Bcl-2 and Bcl-xL: Post-translational modifications
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Mitochondria
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Mitochondrial respiratory chain
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Apocytochrome c and holocytochrome c
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Newmeyer, D.D., and Ferguson-‐Miller, S. Cell 112, 481-‐490, 2003
Mitochondrial Porin or PTP (permeability transition pore)
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Newmeyer, D.D., and Ferguson-Miller, S. Cell 112, 481-490, 2003
OMM permeabilization, PTP, and Mitochondrial fission
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Casp-3/7 may be involved in feedback cyt. c release
Lakhani SA et al., Science 311, 847, 2006 Adrain and Martin Science 311, 785, 2006
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Prodomain Large subunit Small subunit
Linker
p10p20p3-‐26
Prodomains:In executioner caspases: ~3kd In initiator caspases: 10-‐26 kd
Types of caspases: -‐Initiator caspases: caspase-‐2, -‐8, -‐9 and -‐10 -‐Executioner Caspases: caspase-‐3, -‐6 and -‐7
Caspase Structure:
Caspase prodomains:
D. Chandra
Caspases
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Caspases
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Caspases:Executioner caspases
Initiator caspases
Mol. Cell 9, 459-‐470, 2002
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1 479 aa
D374D385
D216
Prodomain (P25) Large subunit (P18)
P55/53DED DED
Small subunit (P12)
P10 subunit
Autocleavage at D385
P43/41
Caspase-8 Cleavage
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Caspase-8 Cleavage
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1 416 aa
D315D330
D130 (casp-3 cleavage site)
CARD domain (P16) Large subunit (P20)
P46CARD
Small subunit (P12)
P10 subunit
Autocleavage at D330
Large subunit + prodomain (P35/P37)
Cleavage at D331 (P22)
Caspase-‐9 Cleavage
Cleavage at D130 = LS + SS (P30)*Prodomain = ~P15
QACGG
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A. Caspase cleavage B. Substrate cleavage
C. Inhibitor effects
Apoptosis: Caspase-‐9 Cleavage
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Holo-cyto. c
-‐COOHApaf-1 CARD NOD WD-‐40 repeats (13)
NH2-‐1 1248
99-‐109 415
Apoptosome-‐mediated caspase-‐9 activation
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Ledgerwood and Morison Clin Cancer Res 2009
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Apoptosis: Caspase-3 activation
A. Caspase cleavage B. Substrate cleavage
C. Inhibitor effects
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Caspase substrates
Proteosome components (Mol Cell 14, 81-‐93, 2004) Mitochondrial complex I p75 subunit (Cell 117, 773-‐786, 2004)
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IAPs
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Shi, Y. Mol. Cell, 9, 459-‐470, 2002
IAPs function as critical prosurvival molecules
*IAPs (especially XIAP) are generally overexpreessed in multiple types of cancer cells
Smac (second mitochondrial activator of caspases)
apoptotic stimulation
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Shi, Y. Mol. Cell, 9, 459-‐470, 2002
Mechanisms of Caspase Activation and Inhibition
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Known apoptotic pathways to activate caspases ! -‐ Intrinsic pathway -‐ Extrinsic pathway or death-‐receptor pathway -‐ Other alternative pathways -‐ Caspase-‐independent apoptosis
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Intrinsic Apoptotic Pathway (mitochondria)
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Extrinsic Apoptotic pathway (death receptor)
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Micheau O. & Tschopp J. Cell 114, 181-‐190, 2003
Extrinsic Apoptotic Pathways
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Crosstalk between two pathways
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How to detect apoptosis ?
-‐Cell morphology by using microscopy -‐Cytochrome c release by immunolabelling and Western -‐Western Blot for caspases and their substrate -‐DAPI and Annexin-‐V-‐staining -‐Detection of apoptosome using gel filtration
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GM701/BMD188 (40 µM)
-Actin
-Holocytochrom
-Holocytochrom
Cytosol
Mito
0 30 � 1h 2h 4
A
Immunolabeling, subcellular fractionation and Western blot
Cells homogenized
Differential centrifugation
Cytosol Mitochondria
SDS-‐PAGE and Western
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Caspase cleavage and DAPI labeling
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Detection of Apoptosome
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What happens to the apoptotic cells?
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What happens to the apoptotic cells?
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Apoptosis and Tumorigenesis
1) Upregulation of Bcl2, BclxL, IAPs, Flip etc. !
2) Downregulation/ mutation of Bax, Bak, BH3-only protein, Death-receptors, Apaf-1 etc.
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Apoptosis based strategies for cancer therapy
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Exploiting apoptotic machinery for cancer therapy
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Chemotherapeutic drugs + Chemopreventive agents
Apoptosis Anti-‐apoptosis/survival Apoptosis pathway pathway pathway
Caspases PI3K/Akt Caspases
NF-‐κB
Xiap, TRAF-‐1, TRAF-‐2, cIAP, Bcl-‐2, BclxL
Combination therapy of chemotherapeutic drugs and Chemopreventive agents will be more beneficial
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Importance of BH3-‐only protein mimetics in cancer therapy
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Take Home message from apoptosis: -‐A predominant form of cell death from worm to mammals -‐Bcl-‐2 family proteins make decision to die or live ! -‐Caspases are the main soldiers in the battle field to execute apoptosis ! -‐Mitochondrion is the center point for all activities ! -‐Targeting Bcl-‐2 family proteins have enormous potential in cancer therapy ! -‐Finding N-‐terminal smac/DIABLO mimetics will counter IAPs ! -‐Applications of death ligands such as TNF-‐α, TRAIL etc. !
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Holo-cyto. c
-‐COOHApaf-1 CARD NOD WD-‐40 repeats (13)
NH2-‐1 1248
99-‐109 415
Shi, Y., Mol. Cell, 9, 459-‐470, 2002
Does release of cytochrome c represent point of no return?
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Holo-cyto. c
-‐COOHApaf-1 CARD NOD WD-‐40 repeats (13)
NH2-‐1 1248
99-‐109 415
Physiological (mM) levels of (deoxy)N
Caspase-9 activation
Chandra D, Bratton SB, Person MD, Tian Y, Martin AG, Ayers M, Fearnhead HO, Gandhi V, and Tang DG. Intracellular nucleotides act as critical prosurvival factors by binding to cytochrome c and inhibiting apoptosome. Cell 125: 1333-‐1346, 2006.
Does release of cytochrome c represent point of no return?
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Holo-cyto. c
-‐COOHApaf-1 CARD NOD WD-‐40 repeats (13)
NH2-‐1 1248
99-‐109 415
Cytochrome c
Apaf-1
Caspase-9
Caspase-3
Apoptosis
Apoptosome Physiological (mM) levels of (deoxy)N
Does release of cytochrome c represent point of no return?
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*Physiological levels of K+ also inhibits cytochrome c-dependent apoptosome formation (JBC, 276, 41985-990, 2001). !*Bao Q, Lu W, Rabinowitz JD, Shi Y. Calcium blocks formation of apoptosome by preventing nucleotide exchange in Apaf-1. Mol Cell. 2007 Jan 26;25(2):181-92.
Does release of cytochrome c represent point of no return?
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Other apoptosis/survival functions of Bcl2-‐family proteins and caspases
• Bcl-‐2 and Bcl-‐xL can also be cleaved by caspases during apoptosis and this cleaved fragments function as proapoptotic proteins.
!• These proteins also undergo posttranslational modifications, which can
also impact on apoptosis sensitivity. !• Pro-‐apoptotic BH3-‐only proteins such as Bad, Bid, Puma, Noxa have also been shown to possess prosurvival roles !• Caspase-‐3 activation is involved in cancer cell invasion !• Caspase-‐8 is required by NF-‐kB activation and promotes cell motility !!
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Caspase-‐independent cell death
Tait and Green, Oncogene 2008
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Autophagy
• First recognized under EM early 1960s. !
• Also called macroautophagy: Self-‐eating to survive. !• A unique form of membrane trafficking in which membrane compartments (autophagosomes) engulf both organelles and cytosolic macromolecules and deliver them to the lysosome for degradation.
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Yoshimori T et al., Cell 128, 833-‐836, 2007 Qu X et al., Cell 128, 931-‐46, 2007
Autophagy
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Martin Lotz, et al. Nat Rev Rheumatol. 2011
Autophagy
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Sagar B. Kudchodkar, et al. Rev Med Virol. 2009
Autophagy
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Mitophagy
Green et al., Science 2011
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Gutian Xiao. Cytokine Growth Factor Rev. 2007
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Autophagy and Cancer
Gutian Xiao. Cytokine Growth Factor Rev. 2007