regulation of apoptosis by bcl-2 family members (prof. thomas kaufmann)
DESCRIPTION
Seminar led by Prof. Thomas Kaufmann. Institute of Pharmacology, University of Bern, Switzerland, at VHIR (15 November 2012). Content: We are interested to investigate the molecular mechanisms by which pro- and anti-apoptotic members of the BCL-2 family regulate the intrinsic (mitochondrial) apoptotic pathway. The pathway is initiated by members of the BH3-only protein subgroup, which act as sensors in response to a variety of intracellular stress stimuli. Some BH3-only proteins, including Bid and Bim, can be activated downstream of death receptors (e.g. Fas/CD95, TNF-R1) and thus mediate a crosstalk from the extrinsic to the mitochondrial apoptotic pathway. We investigate these processes in mouse liver (and more recently also in mouse granulocytes), as hepatocytes strongly rely on this crosstalk for death receptor-induced apoptosis to be effective. We are further interested in the role of 'X-linked inhibitor of apoptosis protein' (XIAP) in these same cell death pathways.TRANSCRIPT
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Regulation of Apoptosis by Bcl-2 Family Members
Thomas KaufmannInstitute of Pharmacology,
University of Bern , [email protected]
Vall d’Hebron Research InstituteNov 15 2012
and XIAP
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Necrosis Apoptosisvs.
2
passive, „accident“,always pathological
active, energy-dependent,physiological + pathophys.
often death of individualcells
whole (parts of) tissue/organ affected
induces inflammationno inflammation,induces tolerance
lysis of cellscells stay intact,
cleared by phagocytosis
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PROGRAMMED CELL DEATH
NECROTIC CELL DEATH“accidents”:- lack of energy- physical damage- chemical damage
Apoptosis
Autophagic Cell Death
Cornification(“keratinization”)
Pyroptosis(casp-1)
Pyronecrosis
Necroptosis(RIPK1/3)
Anoikis
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BCL-2, follicular lymphoma
Tumour Cells Overexpress Anti-Apoptotic Genes
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Follicular Lymphoma (spleen): t(14;18) IgH(14q32) BCL2(18q21)
mantle zone
germinal centre
BCL-2, control
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Effector Caspases(-3, -6 + -7)
Bax/Bak
cytochrome.c Caspase-9/Apaf-1
Bcl-2-like
Apoptosome
BH3-only proteins
cytokine deprivation, DNA- damage, hypoxia, viral infections, ER stress,anoikis, …
XIAP
(Bim, Puma, Bad,...)
(Bcl-2, Mcl-1,Bcl-xL, ...)
XIAP
tBid
Bidcaspase-8
procaspase-8 (-10)
DISC
cFLIPcIAP1/2
Death Receptor (Extrinsic Pathway)
Intrinsic Pathway
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The Bcl-2 Protein Family Regulates the Integrity of the Mitochondrial Outer Membrane
Bax-like
adaptor (APAF-1)
Bcl-2-like
BH3-only
Caspase-9
Bcl-2 Family
Cyt.cSmac/Diablo
XIAP
Caspase-3, -7 (, -6)
+cIAP1,2
MOMPMOMP: mitochondrial outer membrane permeabilisation
Vaux & Silke Nat Rev MCB 2005
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Only XIAP can directly block caspases-3 and -9
Riedl and Shi, Nat Rev MCB 2004
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Selective Interactions Between BH3-Only and Bcl-2-Like Proteins
Bim, Bid, Puma ABT-737
Obatoclax (Nguyen et al PNAS 2007)
(Oltersdorf et al Nature 2005)
Chen et al Mol Cell 2005(modified)
A1
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The Bcl-2 Family – Still Many Open Questions
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BH3-only
Bcl-2-like
Bax/Bak
Strasser, Nat Rev Imm 2005
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BOK: A BAX/BAK-Like Protein?
10
BOK: BCL-2 related ovarian killer (Hsu et al. PNAS 1997)
Ke F. et al., CDD 2012
BOK is widely expressed
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Beroukhim et al., Nature, 2010
BOK is Deleted in Human Cancers with high Frequency
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BOK IS NOT A FUNCTIONAL BAX/BAK HOMOLOGUE
Echeverry et al., in revision
• BOK induces intrinsic apoptosis upstream of BAX/BAK
• BOK localises predominantly to non-mitochondrial sites:– Golgi, ER/nuclear outer membrane– nuclear compartment
• Bok-/- cells present with aberrant ER stress response (part. BFA)
+4-OHT (h):
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Death Receptor-Induced Killing and Crosstalk to Intrinsic (mitochondrial) Apoptotic Pathway
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APOPTOSIS IS ONLY ONE OF SEVERAL POSSIBLE OUTCOMES IN DR SIGNALING
NFkB
Necroptosis
Proliferation
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FADD/C8 (?)
RIP3 RIP1
FLIP
Apoptosis
FADD/TRADD
procaspase-8
TNFa
cIAP1/2
cell survival
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TNF-R1: Not Meant to Kill
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NFkB
Necroptosis
cytokines
RIP3 RIP1
Apoptosis
FADD/TRADD
procaspase-8
cIAP1/2
anti-apoptotic genes=> cell survival
TNF-R1
TNFa
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• Bacterial LPS -> TNFa (Macrophages, Neutrophils, NK T)
• Response via soluble, circulating TNFa TNF-R1 (Pfeffer et al 1993, Rothe et al 1993, Grivennikov et al 2005)
• Sensitisation by D-(+)-galactosamine (GalN)
LPS plus Galactosamine Injection Model of TNF-R1-Mediated Fulminant Hepatitis
Maeda S et al. Immunity 2003
Kaufmann et al. (2009)
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tBidCaspase-8
Cyt.cApaf1/ Caspase-9
Effector Caspases
X?Bax/Bak
Bid
Bcl-2-like
TYPE II
Caspase-8
Effector Caspases
TYPE I
Bid
Hepatocytes are Type II Cells
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The BH3-Only Protein BIM Is Rapidly Phosphorylated in LPS/GalN-Induced Hepatitis
*
Kaufmann et al. Immunity (2009)
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Both BID and BIM are Involved in LPS/GalN-Induced Hepatitis
Kaufmann et al. Immunity (2009)
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BIM is Activated by JNK Mediated Phosphorylation
A
*
B+/- D-JNKI1 (30 mg/kg, i.p.)
Kaufmann et al. Immunity (2009)
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JNK
Bim
Both BID and BIM can Mediate a Crosstalk from Death Receptors to Mitochondria
Corazza et al. JCI (2006)JNK mediated BIM-activationdownstream of TRAIL
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Fas/CD95/Apo-1
• FasL mainly expressed on activated T cells and natural killer cells. • Critical role in the control of the immune system• Fas or FasL-mutant mice develop lymphadenopathy and SLE (systemic
lupus erythematosus)-like disease and are predisposed to lymphoma development
• Many ALPS patients have heterozygous inherited mutations in the Fas gene. (Fisher et al. Cell 1995, Rieux-Laucat et al. Science 1995)
• Only the membrane bound form of FasL is inducing cell death (O’Reilly et al. Nature 2009)
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tBid
Fas
FasL
Caspase-8
Cyt.cApaf1/ Caspase-9
Effector Caspases
X?Bax/Bak
Bid
Bcl-2-like
TYPE II
Caspase-8
Effector Caspases
Fas
FasLTYPE I
Bid
Type I or Type II Fas-Induced Apoptotic Pathway
?
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X
Many Cancer Cells Display a Mandatory Crosstalk
X
?
MOMPX
Bcl-2
XMitochondrium
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Aim: Uncoupling of Death Receptor Pathway
Bcl-2
XMOMP
drugX
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Combination Therapy
Bcl-2
MOMP
ABT-737ABT-737
ABT-737drug X
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- Viral hepatitis- Alcoholic liver disease
- Autoimmune hepatitis- Graft-vs-host disease (GvHD)
- Endotoxin-induced liver failure
- Ischemia/reperfusion-induced liver damage
Importance of Apoptosis in Liver Pathology
-> -> Hepatocellular carcinoma(HCC)
Abnormal apoptosis in hepatocytes is cause or contributing factor in:
death receptors (hepatocytes)
death ligands (activated leukocytes)
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Murine Hepatocytes are Type II-Like Cells
Jo2 anti-Fas – ALT (200 min)
wt bid-/- lpr wt bid-/- lpr
PBS Jo2
Jo2aFas
wt
bid-/-
scale bar: 50 mm
+FasL (0.25 mg/kg)
FasL (crosslinked)
Kaufmann et al. Cell 2007Jost et al. Nature 2009 (modified)
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Lack of BID Blocks Fas-Induced Apoptosis in Type II but not in Type I Cells
Jost PJ et al., 2009 (modified)
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XIAP is Stabilised in Livers of FasL-Treated WT Mice
Jost PJ et al. (2009), modified
+ FasL (0.25 mg/kg)
p<0.05
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Jost PJ et al., 2009
Absence of XIAP Re-Sensitises Bid-Deficient Mice To FasL-Induced Hepatitis
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Absence of XIAP Converts Hepatocytes Into Type I Cells
DEVD-AMC Assay
Jost PJ et al., 2009
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Effects of IAP Antagonistic Drug (BV6) Phenocopies Genetic Loss of XIAP
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Kaufmann, Strasser & Jost, CDD 2011
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mast cell
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Neutrophils: - most frequent leukocyte in human blood- major role in innate immunity- end-differentiated, short-lived- apoptotic clearance of activated
neutrophils essential
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0 24 48 72 960
20
40
60
80
100
untreatedGM-CSF 1ng/mlG-CSF 10ng/mlQ-VD oph 20uM
C57BL/6 WTS
urvi
val (
%)
Time (h)
Primary Neutrophils Die By Classical Apoptosis When Cultured In Vitro
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0 24 48 72 960
20
40
60
80
100
wt untreatedbid-/- untreatedwt TNFabid-/- TNFa
0 24 48 72 960
20
40
60
80
100
wt TNFa
bid-/- TNFa
wt TNFa + Q-VD-oph
bid-/- TNFa + Q-VD-oph
TNFα 50 ng/ml
Q-VD oph 20 μM
Neutrophils die by Apoptosis in Response to High Doses of TNFa
Time (h)
Su
rviv
al %
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FasL Induced Cell Death is Delayed In Bid-/- Neutrophils
Geering et al. Blood 2011
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n>3
FasL Trigger Both Apoptosis and Necroptosis in Neutrophils
0 24 48 72 960
20
40
60
80
100
FasL
FasL + Q-VD-oph
0 24 48 72 960
20
40
60
80
100
FasL + Q-VD-oph
FasL + Q-VD-oph + Nec
0 24 48 72 960
20
40
60
80
100
FasL
FasL + Q-VD-oph
0 24 48 72 960
20
40
60
80
100
FasL + Q-VD-oph
FasL + Q-VD-oph + Nec
Su
rviv
al %
Su
rviv
al %
Su
rviv
al %
Su
rviv
al %
wt
bid-/-
bid-/-
wt
h
FasL 100 ng/ml, Q-VD oph 20 μM, Necrostatin-1 20uM
h
hh
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Loss of BID Aggravates Dextran Sodium Sulfate-Induced Colitis
d0 d1 d2 d3 d4 d5 d6 d7 d8
DSS in drinking water water
an
ima
l we
igh
t (%
)
0 1 2 3 4 5 6 7 885
90
95
100
105
wtbid-/-
* ** ******
***
*n.s.
n.s.
days
=> BID is anti-inflammatory
DSS colitis: -> dependent of neutrophils + macrophages
-> independent of adaptive immune system
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Proinflammatory role for BID?
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Ex Vivo Generation of Neutrophils Using Conditional Hoxb8
d0d5
43
Protocol based on Wang et al. Nature Methods 2006
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Roles of XIAP in Neutrophils
0 24 48 720
20
40
60
80
100
SCF-condHoxb neutrophils
wt TNF-a
XIAP-/- TNF-a
hours
Viab
ility
[%]
TN
Fa
(pg
/ml)
SCF-condHoxb8 neutrophils
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Non-apoptotic roles of XIAP
NOD2
MDP
NFkB
cytokines
XIAP
Damgaard et al. Mol Cell 2012
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IAPs Limit Inflammasome Activation In Macrophages
Vince J. et al. Immunity (2012)
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SUMMARY
• Several poorly characterised BCL-2 family members• Besides BID, BIM can mediate a crosstalk from DR to
mitochondria• XIAP is a crucial discriminator between type I and
type II Fas-induced apoptosis• FasL triggers mix of apoptosis and necroptosis in
neutrophils• Non-apoptotic roles of IAPs and DRs become
increasingly evident (important)
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ACKNOWLEDGMENTS• Philipp Jost (Munich DE)
• Mads Gyrd-Hansen (Kopenhagen, DK)
• Christoph Borner (Freiburg i.Brsg., DE)
• Georg Häcker (Freiburg i. Brsg., DE)
• Thomas Brunner (Konstanz, DE)
• Frank Essmann (Tübingen, DE)
• Julia Fernandez-Rodriguez (Gothenburg, SE)
• Kurt Ballmer (Villigen, CH)
University of Bern (CH)• Nohemy Echeverry• Ursina Gurzeler• Tatiana Rabachini• Daniel Bachmann• Simone Wicki• Nicole Tochtermann• Laetitia Roh
• Hans-Uwe Simon• Mario Tschan• Shida Yousefi• Clemens Dahinden
WEHI, Melbourne (AU)• Andreas Strasser• Francine Ke• Paul Ekert• John Silke • David Huang• Ueli Nachbur
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LUBAC: linear ubiquitin chain assembly complex
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50Andrea L 2009