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APOPTOSIS Dr.Dinesh T Junior resident Department of Physiology JIPMER sclero dinesh
Discussion headings ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
Introduction sclero dinesh
Apoptosis - Definition  ,[object Object],sclero dinesh
Kerr Wyllie and Currie paper, British Journal of Cancer, 1972 Aug;26(4):239-57 "We are most grateful to Professor James Cormack of the Department of Greek, University of Aberdeen, for suggesting this term. The word "apoptosis" (ἁπόπτωσισ) is used in Greek to describe the "dropping off" or "falling off" of petals from flowers, or leaves from trees. To show the derivation clearly, we propose that the stress should be on the penultimate syllable,  the second half of the word being pronounced like "ptosis" (with the "p" silent),  which comes from the same root "to fall", and is already used to describe the drooping of the upper eyelid sclero dinesh
Historical aspects ,[object Object],sclero dinesh
[object Object],sclero dinesh
[object Object],sclero dinesh
[object Object],[object Object],sclero dinesh
Cell death mechanisms Death by suicide   Death by injury sclero dinesh
sclero dinesh APOPTOSIS NECROSIS NATURAL YES NO EFFECTS BENEFICIAL  DETRIMENTAL Physiological or pathological Always pathological Single cells Sheets of cells Energy dependent Energy independent Cell shrinkage Cell swelling Membrane integrity maintained Membrane integrity lost
sclero dinesh APOPTOSIS NECROSIS Role for mitochondria and cytochrome C No role for mitochondria No leak of lysosomal enzymes Leak of lysosomal enzymes Characteristic nuclear changes Nuclei lost Apoptotic bodies form Do not form DNA cleavage No DNA cleavage Activation of specific proteases No activation Regulatable process Not regulated Evolutionarily conserved Not conserved Dead cells ingested by neighboring cells Dead cells ingested by neutrophils and macrophages
Significance of apoptosis ,[object Object],[object Object],[object Object],sclero dinesh
Etiopathogenesis sclero dinesh
Why should a cell commit suicide? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
[object Object],[object Object],[object Object],sclero dinesh
Apoptosis:  in embryogenesis Morphogenesis (eliminates excess cells): Selection (eliminates non-functional cells): sclero dinesh
Apoptosis:  in embryogenesis Immunity (eliminates dangerous cells): Self antigen recognizing cell Organ size (eliminates excess cells): sclero dinesh
Apoptosis:  importantance in adults Tissue remodeling (eliminates cells no longer needed): Virgin mammary gland Late pregnancy, lactation Involution (non-pregnant, non-lactating) Apoptosis Apoptosis -  Testosterone Prostate gland  sclero dinesh
Apoptosis:  importantance in adults Tissue remodeling (eliminates cells no longer needed): Resting lymphocytes + antigen (e.g. infection)  - antigen (e.g. recovery)  Apoptosis sclero dinesh
[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
[object Object],[object Object],[object Object],sclero dinesh
[object Object],[object Object],sclero dinesh
[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
[object Object],[object Object],Fig. 1:   SC-1 induced apoptosis in stomach carcinoma cells         Left: Before induction         Middle: 24h after induction          Right: 48h after induction sclero dinesh
Morphological & Biochemical changes sclero dinesh
Classic changes ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
Histology ,[object Object],[object Object],[object Object],sclero dinesh
Bio chemical changes sclero dinesh
Mechanisms of apoptosis  sclero dinesh
sclero dinesh
sclero dinesh
Caspases  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
Initiation ,[object Object],[object Object],[object Object],[object Object],sclero dinesh
STAGES OF CLASSIC APOPTOSIS Healthy cell DEATH SIGNAL / STIMULI (extrinsic or intrinsic) Commitment to die  (reversible) EXECUTION (irreversible) Dead cell (condensed, crosslinked) ENGULFMENT (macrophages, neighboring cells) DEGRADATION sclero dinesh
Receptor pathway (physiological): Death receptors: (FAS, TNF-R, etc) FAS ligand TNF Death domains Adaptor proteins Pro-caspase 8 (inactive) Caspase 8 (active) Pro-execution caspase (inactive) Execution caspase (active) Death MITOCHONDRIA sclero dinesh
Apoptosis triggered by external signals: the extrinsic or death receptor pathway sclero dinesh
Regulation of apoptosis ,[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
Intrinsic pathway (damage): Mitochondria Cytochrome c release Pro-caspase 9 cleavage Pro-execution caspase (3) cleavage Caspase (3) cleavage of cellular proteins, nuclease activation,  etc.  Death BAX BAK BOK BCL-Xs BAD BID B IK BIM NIP3 BNIP3 BCL-2 BCL-XL BCL-W MCL1 BFL1 DIVA NR-13 Several viral proteins sclero dinesh
sclero dinesh
sclero dinesh
Intracellular signals Oxidative damage from free radicals, Radiation, Virus infection, Nutrient deprivation, Pro-apoptotic Factors Damage to the mitochondrial membrane increasing permeability Entry of Cytochrome C into the cytoplasm Cytochrome C binds to Apaf-1 forming an apoptosome Apoptosome activates procaspase-9 to caspase-9 Caspase-9 cleaves and activates caspase-3 and caspase-7. This executioner caspases activate a cascade of proteolytic activity that leads to: Chromatin condensation, DNA fragmentation, Protein cleavage, Membrane permeability sclero dinesh
sclero dinesh
Physiological  Intrinsic receptor pathway  damage pathway  MITOCHONDRIAL SIGNALS Caspase cleavage cascade Orderly cleavage of proteins and DNA CROSSLINKING OF CELL CORPSES; ENGULFMENT (no inflammation) sclero dinesh
Steps  sclero dinesh
Disorders of apoptosis sclero dinesh
Apoptosis:  Role in Disease  TOO MUCH:  Tissue atrophy TOO LITTLE:  Hyperplasia Neurodegeneration Thin skin etc Cancer Athersclerosis etc sclero dinesh
Apoptosis:  Role in Disease Neurodegeneration ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
Apoptosis: Role in Disease Cancer ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
[object Object],[object Object],Apoptosis: Role in Disease Cancer sclero dinesh
[object Object],[object Object],Apoptosis: Role in Disease Cancer sclero dinesh
Apoptosis:  Role in Disease Aging Aging --> both too much and too little apoptosis (evidence for both) Too much (accumulated oxidative damage?) ---> tissue degeneration Too little (defective sensors, signals? --->  dysfunctional cells accumulate hyperplasia (precancerous lesions) sclero dinesh
Apoptosis: Role in Disease ,[object Object],[object Object],sclero dinesh
[object Object],[object Object],[object Object],[object Object],[object Object],sclero dinesh
Conclusion sclero dinesh
Cells are balanced between life and death DAMAGE Physiological death signals DEATH SIGNAL PROAPOPTOTIC PROTEINS (dozens!) ANTIAPOPTOTIC PROTEINS (dozens!) DEATH sclero dinesh
Thank u…. sclero dinesh

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Apoptosis

  • 1. APOPTOSIS Dr.Dinesh T Junior resident Department of Physiology JIPMER sclero dinesh
  • 2.
  • 4.
  • 5. Kerr Wyllie and Currie paper, British Journal of Cancer, 1972 Aug;26(4):239-57 "We are most grateful to Professor James Cormack of the Department of Greek, University of Aberdeen, for suggesting this term. The word "apoptosis" (ἁπόπτωσισ) is used in Greek to describe the "dropping off" or "falling off" of petals from flowers, or leaves from trees. To show the derivation clearly, we propose that the stress should be on the penultimate syllable, the second half of the word being pronounced like "ptosis" (with the "p" silent), which comes from the same root "to fall", and is already used to describe the drooping of the upper eyelid sclero dinesh
  • 6.
  • 7.
  • 8.
  • 9.
  • 10. Cell death mechanisms Death by suicide Death by injury sclero dinesh
  • 11. sclero dinesh APOPTOSIS NECROSIS NATURAL YES NO EFFECTS BENEFICIAL DETRIMENTAL Physiological or pathological Always pathological Single cells Sheets of cells Energy dependent Energy independent Cell shrinkage Cell swelling Membrane integrity maintained Membrane integrity lost
  • 12. sclero dinesh APOPTOSIS NECROSIS Role for mitochondria and cytochrome C No role for mitochondria No leak of lysosomal enzymes Leak of lysosomal enzymes Characteristic nuclear changes Nuclei lost Apoptotic bodies form Do not form DNA cleavage No DNA cleavage Activation of specific proteases No activation Regulatable process Not regulated Evolutionarily conserved Not conserved Dead cells ingested by neighboring cells Dead cells ingested by neutrophils and macrophages
  • 13.
  • 15.
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  • 18.
  • 19. Apoptosis: in embryogenesis Morphogenesis (eliminates excess cells): Selection (eliminates non-functional cells): sclero dinesh
  • 20. Apoptosis: in embryogenesis Immunity (eliminates dangerous cells): Self antigen recognizing cell Organ size (eliminates excess cells): sclero dinesh
  • 21. Apoptosis: importantance in adults Tissue remodeling (eliminates cells no longer needed): Virgin mammary gland Late pregnancy, lactation Involution (non-pregnant, non-lactating) Apoptosis Apoptosis - Testosterone Prostate gland sclero dinesh
  • 22. Apoptosis: importantance in adults Tissue remodeling (eliminates cells no longer needed): Resting lymphocytes + antigen (e.g. infection) - antigen (e.g. recovery) Apoptosis sclero dinesh
  • 23.
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  • 26.
  • 27.
  • 28. Morphological & Biochemical changes sclero dinesh
  • 29.
  • 30.
  • 31. Bio chemical changes sclero dinesh
  • 32. Mechanisms of apoptosis sclero dinesh
  • 35.
  • 36.
  • 37. STAGES OF CLASSIC APOPTOSIS Healthy cell DEATH SIGNAL / STIMULI (extrinsic or intrinsic) Commitment to die (reversible) EXECUTION (irreversible) Dead cell (condensed, crosslinked) ENGULFMENT (macrophages, neighboring cells) DEGRADATION sclero dinesh
  • 38. Receptor pathway (physiological): Death receptors: (FAS, TNF-R, etc) FAS ligand TNF Death domains Adaptor proteins Pro-caspase 8 (inactive) Caspase 8 (active) Pro-execution caspase (inactive) Execution caspase (active) Death MITOCHONDRIA sclero dinesh
  • 39. Apoptosis triggered by external signals: the extrinsic or death receptor pathway sclero dinesh
  • 40.
  • 41. Intrinsic pathway (damage): Mitochondria Cytochrome c release Pro-caspase 9 cleavage Pro-execution caspase (3) cleavage Caspase (3) cleavage of cellular proteins, nuclease activation, etc. Death BAX BAK BOK BCL-Xs BAD BID B IK BIM NIP3 BNIP3 BCL-2 BCL-XL BCL-W MCL1 BFL1 DIVA NR-13 Several viral proteins sclero dinesh
  • 44. Intracellular signals Oxidative damage from free radicals, Radiation, Virus infection, Nutrient deprivation, Pro-apoptotic Factors Damage to the mitochondrial membrane increasing permeability Entry of Cytochrome C into the cytoplasm Cytochrome C binds to Apaf-1 forming an apoptosome Apoptosome activates procaspase-9 to caspase-9 Caspase-9 cleaves and activates caspase-3 and caspase-7. This executioner caspases activate a cascade of proteolytic activity that leads to: Chromatin condensation, DNA fragmentation, Protein cleavage, Membrane permeability sclero dinesh
  • 46. Physiological Intrinsic receptor pathway damage pathway MITOCHONDRIAL SIGNALS Caspase cleavage cascade Orderly cleavage of proteins and DNA CROSSLINKING OF CELL CORPSES; ENGULFMENT (no inflammation) sclero dinesh
  • 47. Steps sclero dinesh
  • 48. Disorders of apoptosis sclero dinesh
  • 49. Apoptosis: Role in Disease TOO MUCH: Tissue atrophy TOO LITTLE: Hyperplasia Neurodegeneration Thin skin etc Cancer Athersclerosis etc sclero dinesh
  • 50.
  • 51.
  • 52.
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  • 54.
  • 55. Apoptosis: Role in Disease Aging Aging --> both too much and too little apoptosis (evidence for both) Too much (accumulated oxidative damage?) ---> tissue degeneration Too little (defective sensors, signals? ---> dysfunctional cells accumulate hyperplasia (precancerous lesions) sclero dinesh
  • 56.
  • 57.
  • 59. Cells are balanced between life and death DAMAGE Physiological death signals DEATH SIGNAL PROAPOPTOTIC PROTEINS (dozens!) ANTIAPOPTOTIC PROTEINS (dozens!) DEATH sclero dinesh