apoptosis
TRANSCRIPT
Apoptosis
SUBMITED BY
AMIT KUMAR
MPHARM (I Year)
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In humans, the rate of cell growth and cell death is balanced to
maintain the weight of the body.
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Life cannot exist without cellular death
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Cell death can occur via several processes (about 11 type):
1. Apoptosis
2. Necrosis
3. Autophagy
4. Entosis
5. Oncosis
6. Pyroptosis
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11.
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Apoptosis = “normal” or “programmed” cell death
Apoptosis is the physiological cell death which
unwanted or useless cells are eliminated during
development and other normal biological processes.
Necrosis = “accidental” or “ordinary” cell death
Necrosis is the pathological cell death which occurs
when cells are exposed to a serious physical or chemical
insult (hypoxia, hyperthermia, ischemia).
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1) Cellular condensation
2) Membranes remain intact
3) Requires ATP
4) Cell is phagocytosed, no tissue
reaction
5) Ladder-like DNA
fragmentation
6) In vivo, individual cells appear
affected
1) Cellular swelling
2) Membranes are broken
3) ATP is depleted
4) Cell lyses, eliciting an
inflammatory reaction
5) DNA fragmentation is
random, or smeared
6) In vivo, whole areas of the
tissue are affected
Necrosis Apoptosis
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The word ‘‘apoptosis’’ comes from the
ancient Greek, meaning the:
‘‘falling of petals from a flower’’ or
‘‘of leaves from a tree in autumn’’
In 1964 Lockshin, study on programmed cell death.
The term apoptosis (a-po-toe-sis) was first used in a
now-classic paper by Kerr et al 1972 to describe a
morphologically distinct form of cell death.
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Apoptosis or programmed cell death (PCD) is a mode of cell
death that occurs under normal physiological conditions and
the cell is an active participant in its own demise (“cellular
suicide”).
It is important for the development of multicellular organism
(embryonic development) and homeostasis of their tissues
(adult).
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1) Cell shrinkage
2) Organelle reduction
3) Mitochondrial leakage
4) Chromatin condensation
5) Nuclear fragmentation
6) Membrane blebbing & changes
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Mitochondrial leakage
Organelle
reduction
Cell
shrinkage
Nuclear
fragmentation
Chromatin condensation
Membrane blebbing & changes
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Characteristic biochemical changes in cells undergoing
apoptosis
1)Chromosomal DNA cleaved into fragments
2)Change in the plasma membrane – phosphatidylserine
in the outer leaflet
3)Loss of electrical potential across the inner membrane of the
mitochondria
4)Relocation of cytochrome c from the intermembrane space of
the mitochondria to the cytosol
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Apoptosis is a beneficial and important phenomenon:
In embryo
1. During embryonic development, help to digit formation.
Lack of apoptosis in humans
can lead to webbed fingers
called “syndactyly ”.
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2. Normal event in development of the nervous system
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In adult
Normal cell turn over
Tissue homeostasis
Induction and maintenance of immune tolerance
Development of the nervous system
Endocrine-dependent tissue atrophy
Elimination of activated, damaged and abnormal cells
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In animals
Embryonic Chicken Foot
Embryonic Mouse Paw
Tail absorption of the tadpole
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APOPTOSIS
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Extrinsic pathway (death receptor- mediated events)
Intrinsic pathway (mitochondria- mediated events)
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Death Receptors
Death Ligands
Adaptor Proteins
Caspaseses
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“Death receptors” that are members of the tumor necrosis factor
(TNF) receptor superfamily.
Death receptors have a cytoplasmic domain of about 80
amino acids called the “death domain”.
This death domain plays a critical role in transmitting the death
signal from the cell surface to the intracellular signaling
pathways.
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The best characterized receptors & ligands corresponding
death receptors include:
FasR (CD95/APO1) FasL
DR3 Apo3L
DR4 (TRAIL-R1) Apo2L
DR5 (TRAIL-R2) Apo2L
TNFR1 TNF-α
TNFR2 TNF-ß
LigandsReceptors
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Apoptotic adaptor proteins play a critical role in
regulating pro- and anti-apoptotic signalling
pathways
Adaptor proteins;
1)FADD (Fas-associated death domain)
2) TRADD (TNF receptor-associated death domain), are
recruited to ligand-activated, oligomerized death receptors
to mediate apoptotic signalling pathways.
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Caspases= Cysteinyl aspartate specific proteases
A family of intracellular cysteine proteases that play a pivotal
role in the initiation and execution of apoptosis.
At least 14 different members of caspases in mammalian cells
have been identified
All are synthesized as inactive proenzymes (zymogen) with
32-56 kDa
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To date, ten major caspases have been identified and broadly categorized into:
Signaling or Initiator caspases
Effector or Executioner caspases
Inflammatory caspases
The other caspases that have been identified include:
Caspases
Central role in cascade of apoptotic events is played by
caspase 3 (CPP32)
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Bcl-2 family proteins
Cytochrome c
Apoptosome
Caspaseses
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The control & regulation of apoptotic mitochondrial events occurs
through members of the Bcl-2 family of proteins
Anti-apoptotic proteins include Bcl-2, Bcl-x, Bcl-XL, Bcl-w
Pro-apoptotic proteins include Bax, Bak, Bid, Bad, Bim, Bik
The main mechanism of action of the Bcl-2 family of proteins
is the regulation of cytochrome c release from the
mitochondria via alteration of mitochondrial membrane
permeability.
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Cytochrome c is an abundant protein of the mitochondrial inner
membrane, and acts as an electron transport intermediate.
During apoptotic activation lead to alterations in permeability of
the mitochondrial membrane pore proteins and release of
cytochrome c.
Cytochrome c binds and activates Apaf-1 as well as
procaspase-9, forming an “apoptosome”.
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The stimuli that initiate the intrinsic pathway produce intracellular
signals such as radiation (DNA damage), absence of certain growth
factors, hormones and cytokines.
All of these stimuli cause changes in the mitochondrial outer
membrane permeabilization (MOMP)
Release of pro-apoptotic proteins such as cytochrome c,
Smac/DIABLO, AIF, endonuclease G and CAD from the inter-
membrane space into the cytosol.
Cytochrome c binds and activates Apaf-1 as well as
procaspase-9, forming an “apoptosome”.
Caspase-9 activation, subsequent caspase-3 activation and
cell death.
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Assay for apoptosis
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Apoptosis assays, based on
methodology, can be classified into six
major groups:
1. Cytomorphological alterations
2. DNA fragmentation
3. Detection of caspases, cleaved
substrates, regulators and inhibitors
4. Membrane alterations
5. Detection of apoptosis in whole mounts
6. Mitochondrial assays
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The evaluation of hematoxylin and eosin-stained tissue sections
with light microscopy does allow the visualization of apoptotic
cells.
This method detects the later events of apoptosis
TEM is considered the gold standard to confirm apoptosis:
1) Electron-dense nucleus
2) Nuclear fragmentation
3) Disorganized cytoplasmic organelles
4) large clear Vacuoles
5) Intact cell membrane
6) Blebs at the cell surface
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DNA fragmentation occurs in the later phase of apoptosis.
TUNEL (Terminal dUTP Nick End-Labeling) assay quantifies
the incorporation of deoxyuridine triphosphate (dUTP) at single and
double stranded DNA breaks in a reaction catalyzed by the template
independent enzyme, terminal deoxynucleotidyl transferase (TdT).
Incorporated dUTP is labeled such that breaks can be quantified
either by flowcytometry, fluorescent microscopy, or light
microscopy.
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TUNEL positive cell
TUNEL negative cell
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During the process of apoptosis, one of the earliest events is
Externalization of Phosphatidylserine (PS) from the inner to the
outer plasma membrane of apoptotic cells.
These cells can be demonstrated by bound with Fluorescein
isothyocyanate (FITC)-labeled Annexin V and detected with
fluorescent microscopy.
The vital dye propidium iodide (PI) should be used in
combination of annexin V that help in distinguish viable , apoptotic
& necrotic cell populations at the same time.
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Apoptosis can also be visualized in whole mounts of embryos
or tissues using dyes such as acridine orange (AO), Nile blue
sulfate (NBS), and neutral red (NR).
Since these dyes are acidophilic, they are concentrated in areas
of high lysosomal and phagocytotic activity.
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Mitochondrial assays and cytochrome c release allow the
detection of changes in the early phase of the intrinsic pathway.
The mitochondrial outer membrane (MOM) collapses during
apoptosis, allowing detection with a fluorescent cationic dye.
Cytochrome c release from the mitochondria can also be assayed
using fluorescence and electron microscopy in living or fixed cells.
Apoptotic or anti-apoptotic regulator proteins such as Bax, Bid,
and Bcl-2 can also be detected using fluorescence and confocal
microscopy
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BCL2 inhibitors;
1)G3139 is an antisense oligodeoxynucleotide
targeting BCL2 mRNA resulting in RNAse H activation.
2)ABT263 is a small molecule mimetic of the BH3 domain of
the pro-apoptotic BAD protein that is currently in clinical trial in
chronic lymphatic leukaemia.
Caspaseinhibitors;
1) VX-765 is an orally active, reversible caspase-1 inhibitor that
was being developed for the treatment of inflammatory disorders.
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2) Emricasan is a novel, irreversible, orally active pan-caspase
inhibitor that has been investigated for the treatment of chronic
HCV infection and liver transplantation rejection.
3) NCX-1000, a small-molecule inhibitor that selectively inhibits
caspase-3, -8 and -9 in the micromolar range, was in phase II
clinical trials for the treatment of chronic liver disease.
4) PAC-1, a small molecule that induces both procaspase-3
activation in vitro and apoptosis in several cancer cell lines.
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با تشکر
Thanks for your attention
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