2013programmed cell dealth r
TRANSCRIPT
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Programmed cell death and embryonic development
Dept. of Histology & Embryology
Xiangya School of Medicine, CSU
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Definition of Programmed Cell Death
programmed cell death - llec fo epyt a
dezilaiceps sesu llec eht hcihw ni htaed
edicius llec a ;flesti llik ot yrenihcam ralullec
lortnoc ot snaozatem selbane taht msinahcem
netaerht taht sllec etanimile dna rebmun llec
lavivrus s'lamina eht
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1885 Flemming first mentioned cell death in rabbit ovarian follicle (chromatolysis) is physiological, and described chromatin was condensed into half-moon shape (crescent);
1914 Gräper: Chromatolysis of all cells eliminated from organs; phagocytosis of neighboring cells; exploring the phenomenon the organ construction;
1951 Glucksmann reviewed cell death in ontogenesis; a normal part of animal development, and detailed the process of chromatolysis;
1964 Lockshin & Williams proposed the concept of "programmed cell-death" in their research thesis related to insect (silkworm moth) metamorphosis
Important events in the history of cell death
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1966 Saunders: “The death clock is ticking;” cell death is a suicide
1972 Kerr, Wyllie, Currie: Apoptosis is general in morphology and among animals
Important events in the history of cell death
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Sydney Brenner of the Salk Institute used the nematode Caenorhabditis elegans, which became a multicellular model experimental system, to follow cell division and differentiation from the fertilized egg to the adult via microscopic observation. He demonstrated that a specific gene mutation, induced by ethyl methane sulfonate, could be linked to a specific effect in nematode organ development. His work on nematodes created an experimental system that laid the foundation for the study of apoptosis.
John Sulston of the Wellcome Trust Institute in England mapped cell lineages, where every cell division and differentiation could be followed in the development of C. elegans. There are only 959 cells in an adult nematode (1090 to 959 cells, 131 cell lost). He showed that specific cells lineages (nerves) undergo programmed cell death, as an integral part of the normal differentiation process.
Robert Horvitz of MIT discovered and characterized key genes controlling cell death in C. elegans. He identified the first two bona fide "death genes", ced-3 and ced-4. Functional ced-3 & ced-4 genes are a prerequisite for cell death to be executed. Another gene, ced-9, protects against cell death by interacting with ced-3and ced-4. He has shown how these genes interact with each other in the cell death process and that corresponding genes (a ced-3-like gene) exists in humans.
The Nobel Prize in Physiology or Medicine 2002
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Sydney Brenner H. Robert Horvitz John Sulston
THE 2002 NOBEL PRIZE WINNER
PCD has been the subject of increasing attention and research
efforts. This trend has been highlighted with the award of the
2002 Nobel Prize in Physiology or Medicine to Sydney Brenner
(United Kingdom), H. Robert Horvitz (US) and John E. Sulston
(UK)
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The creation of the conception of PCD
Carroll Williams was always known for his colorful phraseology, and as graduate students we always tried to emulate him. Because computers were just beginning to be talked about at the time, programmed cell death seemed to be a particularly modern and colorful way of describing what we saw. It was a metaphor stating what I thought was pretty obvious — if a biological process occurs at a defined location and time, then it must in some fashion be programmed or written into the genetics of the organism-----from Williams’ student .
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PCD and APOPTOSIS
Apoptosis is used as a synonym for PCD
Apo: apart
Ptosis: fallen
Shedding of leaves from trees
During embriogenesis ------ occurs as PCD
Post-embrional life------- as apoptosis
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PCD and its significance during embryonic development
Optimization of system matching
To regulate the cell number by eliminating wasted, useless,
unwanted, or crippled cells!
For example, 80% nerve cells, 70-95% oocyte died in this way.
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Sculpting of tissues
Such as the formation of the fingers and toes of
the fetus in chicken, mouse or human.
Arrowheads indicate PCD cells. PCD in duck or tortoise
Indicated by arrow
PCD and its significance during embryonic development
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Shortening and rotation
of the myocardial portion
of the OFT(outflow tract
(OFT)) coincident with
cardiomyocyte apoptosis
Sculpting of tissues
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Extensive postnatal apoptosis occurs invessels that regress after birth, ie, ductus arteriosus and the umbilical arteries
Removal of transitional or
useless structures
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Deletion of
transitional
structures
Evolution of aortic arches
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Deletion of transitional structures
Pronephros-
pronephric tubule and
duct
Mesonephros-
mesonephric tubule
and duct
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Tadpole tail removed by apoptosis during development
Deletion of transitional structures
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•Autoreactive T cells with the
potential to attack "self" are
removed by apoptosis
Self antigenrecognizing cell
Essential for the removal of
cells that threaten homeostasis
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Morphological changes during apoptosis
Cell shrinkage
Apoptotic B Cells
Hoechst stainingHE staining
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Morphological features of Morphological features of
apoptosisapoptosis
Membrane blebbing
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macrophage
Apoptoti
c bodies
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Biochemical changes during apoptosis
Phosphatidylserine inside outannexin V, a Ca+ dependent PS binding protein
Annexin V staining
flow cytometry
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Activation of Caspase dependent endonuclease (CAD).
Biochemical changes during apoptosis
180-200bp
DNA “ladder”
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Biochemical changes during apoptosis
Terminal deoxynucleotidyl transferase (TDT) mediated dUTP nick end labeling(TUNEL)Principle: TdT mediates incorporation of biotinylated dUTP into 3’ OH ends of fragmented DNA
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Biochemical changes during apoptosis
Proteins in favor for apoptosis ↑
Death receptor superfamily, such as TNFR1
, Fas/APO-1, DR,3,4 and 5, and so on
Caspase family (cysteine-containing aspartate-specific
protease): Caspase 1-10,13. 11 and 12 species specific
Apaf-1 (apoptotic protease activating factor-1)
Mitochondrial membrane releasing factors: Smac/
DIABLO
Proteins against apoptosis ↑Bcl-2 family (B cell lymphoma/Leukemia-2, Bcl-2), but BAX
subfamily in favor of apoptosis
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Cell Death Pathways
Death
Execution
IAPs
Smac/
DIABLO
AIF
Endonuclease
activation
DNA broken
Death
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Harmful factor→ changes of ER Ca2+ stable status and accumulation of incorrect folding proteins→pro-caspase-12→ caspase-12→BAX activated→mitochondria →Cyt C and Apaf1 release→ caspase9 activated→caspase-3 activated→apoptosis
Endoplasmic reticulum (ER) pathway
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Hormones regulate PCD during embryonic development
The loss of tadpole tail is controlled by thyroxine
The PCD of thymocyte is regulated by Glucocorticoid
The regression of paramesonephric duct/ Muller duct is controlled by
Mullerian inhibiting substance
Estrogen inhibits PCD of Granulosa cells
FSH/LH inhibit PCD of ovarian follicle
Insulin inhibits PCD of lens epithelial cells
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Growth factors/cytokins regulate PCD during embryonic development
Lack of NGF,FGF ,TGF,G-CSF leads to
PCD
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Necrosis
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Necrosis vs. Apoptosis
Cellular condensation
Membranes remain intact
Requires ATP
Cell is phagocytosed, no
tissue reaction
Ladder-like DNA
fragmentation
In vivo, individual cells
appear affected
Active death
• Cellular swelling
• Membranes are broken
• ATP is depleted
• Cell lyses, eliciting an
inflammatory reaction
• DNA fragmentation is
random
• In vivo, whole areas of
the tissue are affected
• Passive death
Necrosis Apoptosis
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Questions
Can you imagine how it likes about DNA gel
electrophoresis from extracts of necrotic tissue?
TUNEL also labels necrotic cells?
Autophagy, 3rd cell death
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31
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Receptor pathway (physiological):
Death receptors:
(FAS, TNF-R, etc)
FAS ligand TNF
Deathdomains
Adaptor proteins
Pro-caspase 8 (inactive) Caspase 8 (active)
Pro-execution caspase (inactive)Execution caspase (active)
DeathMITOCHONDRIA
zymogen enzyme
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H2O2
Growth factor
receptors
casp9Bcl2
PI3KAkt
BAD
Apaf1
Cyt.CATP
The mitochondrial pathway
casp3
casp3
IAPs
Smac/
DIABLO
AIF
Bax
Bax
p53
Fas
Casp8
Bid
Bid
Bid
DNA
damage