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1. Cell Responses 3. Cell Death Dr.T.Krishna MD, www.mletips.com 1
2. Lecture Plan Cell death
Apoptosis
Necrosis
Example of Cell injury & death
Ischemia & Hypoxia
Chemicals & Drugs
2 Dr.T.Krishna MD, www.mletips.com
3. Dr.T.Krishna MD, www.mletips.com 3 Cell InjuryCell Injury
4. Necrosis Definition:
spectrum of morphologic changes that follow cell death in living tissue, largely resulting from the progressive degradative action of enzymes on the lethally injured cell
Morphology
LM (light Microscopy)
Increased eosinophilia
Myelin figures
Calcification of dead cells
EM (Electron Microscopy)
Cytoplasm
Membrane discontinuities
large amorphous mitochondria densities
Aggregates of fluffy material (denatured protein)
Nucleus
Pyknosis (nuclear shrinkage and increased basophilia also seen in apoptotic cell death)
Karyorrhexis (fragmentation)
Karyolysis (breakdown of DNA by DNase activity)
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5. Necrosis Types
1. Coagulative = preservation of the basic outline of necrotic cell
Mechanism protein denaturation
characteristic of hypoxic cell death in all tissues (except Brain)
Best example MI
2. Liquefactive= Cell outlines are obscured & Replaced by yellow pus
Mechanism bacterial/fungal enzymatic digestion & inflammatory response
Whatever is the stimulus in brain it is always Liquefactive
Gangrene surgical term
5 Dr.T.Krishna MD, www.mletips.com
6. Necrosis Types
3. Caseous =
distinctive form of Coagulative necrosis but tissue architecture is completely lost
MC in TB (also in fungal)
Meaning - cheesy white gross appearance of necrosis
Microscopy - granulomatous reaction
(what is granulomatous reaction?)
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7. Necrosis Types
4. Fat Necrosis =
not a specific pattern
Grossly - chalky white areas of calcium & fatty acids(fat saponification)
Seen in acute pancreatitis & trauma of breast
Ghost cells are seen in microscopy
7 Dr.T.Krishna MD, www.mletips.com
8. Examples of cell injury and death 1. Ischemia & Hypoxia
MC type of cell injury in clinical medicine
Ischemic injures faster than hypoxia
Reperfusion injury cell injury following restoration of blood flow to the ischemic cells
Mechanism of cell death predominately necrosis in ischemia ( apoptosis is important in reperfusion injury by reactive free radicals, complements, IgM)
2. Chemicals & drugs
Mechanisms
1. Directly acting on cell structures
Mercuric chloride binds sulfhydral (SH) groups of membranes and proteins
Cyanide binds and inactivates mitochondrial cytochrome oxidase
Anti- neoplastic and antibiotics- act on genetic material & proteins 8 Dr.T.Krishna MD, www.mletips.com
9. Examples of cell injury and death 2. Chemicals & drugs
Mechanisms
i). Directly acting on cell structures
ii). Indirectly acting
Convert into active toxic metabolites by p-450 oxidases
Mechanisms by reactive free radicals
Examples Carbon tetrachloride & Acetaminophen (Tylenol)
Carbon tetrachloride (CCl4) = is converted into CCl3? CCl3 is a free radical ? inhibits apoprotein synthesis ? accumulation of Hepatic Lipoproteins (Fatty Liver) and causes auto oxidation of polyenoic fatty acids of membranes
Acetaminophen (Tylenol) = active toxic metabolites produced in liver ? binds and with reduced glutathione peroxidase (GSH) ; large doses of Tylenol depletes GSH and lead to free radical damage of liver (hepatic failure)
9 Dr.T.Krishna MD, www.mletips.com
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11. Apoptosis Morphology LM- (H&E)
Single cells or small clusters of cells
Round or oval mass of intensely Eosinophilic cytoplasm with dense nuclear chromatin fragments
EM
Cell shrinkage, Chromatin condensation-most characteristic feature ,Phagocytosis, cytoplasmic blebs and apoptotic bodies
Severity of stimulus determines the form of death
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12. Apoptosis Molecular/Biochemical changes Protein Cleavage-
By cysteine proteases / caspases
First into larger pieces (50- 300 Kb) and later into Olig-onucleosomes (180 - 200 bp)
In agarose gel electrophoresis
Apoptosis is seen as DNA ladders (necrosis as smear pattern)
Apoptotic cells express phosphatidylserine, thrombospondin ( adhesive glycoprotein)
Macrophages recognize these cells early ? phagocytosis without inflammation
12 Dr.T.Krishna MD, www.mletips.com
13. Apoptosis Mechanisms Apoptosis was studied in a Nematode Caenorhabditis elegans (C. elegans)
C. elegans shows programmed cell growth followed by cell death
specific genes (called ced genes, for cell death abnormal) in mutant worms initiate or inhibit apoptosis
Initiation phase- caspases activation
1. Extrinsic/ receptor-initiated pathway
2. Intrinsic/ mitochondrial pathway
Execution phase- enzymes cause cell death
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14. Apoptosis Mechanisms Extrinsic Pathway
(Death Receptor- Initiated)
initiated by involvement of cell surface death receptors (TNF-family ) on cells
TNFR1, related protein - Fas (CD95) - cytoplasmic domain (death domain) 14 Dr.T.Krishna MD, www.mletips.com
15. Apoptosis Molecular/Biochemical changes Intrinsic Pathway
(Mitochondrial)
No role for death receptors
Growth factors & other signals stimulate
Bcl2 family
Anti-apoptotic members - Bcl2 and Bcl -x
Pro-Apoptotic members
- Bak, Bax, and Bim
Present in mitochondrial membranes and the cytoplasm 15 Dr.T.Krishna MD, www.mletips.com
16. Dr.T.Krishna MD, www.mletips.com 16 Executioner
caspasesExecutioner
caspases
17. Apoptosis Caspases Proteases present in the form of Pro-enzyme forms (Zymogens)
C- cysteine protease (aspase- cleave after aspartic acid in the polypeptide chain)
Types
initiators- Caspases 8, 9
Executioners - Caspases 3, 6
>20 members
Activated by other & own (autocatalysis)
In nucleus, Caspases act on proteins involved in
Transcription
DNA replication
DNA repair
Example: Caspase 3 DNAase activation (Inter nucleosomal cleavage) 17 Dr.T.Krishna MD, www.mletips.com
18. Apoptosis Removal of Dead Cells Apoptotic cells release Soluble factors
Marker molecules are expressed on surface of apoptotic cell or fragments
Markers are immediately recognized by macrophages
Macrophages also secrete substances which bind only to apoptotic cells
Viable cells express molecules (CD- 31) and avoid getting phagocytosed
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19. Apoptosis Examples 1. After growth factor deprivation
Lymphocytes not stimulated by Ag/Cytokine
Intrinsic pathway plays important role
Mediated by Pro- Apoptotic Bcl2 family
2. DNA damage (Genotic stress)
Chemicals
Radiation
P53 accumulation? trnscriptional activation of Bcl2 genes ?activation of Caspases
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20. Apoptosis- Examples contd.. 3. Apoptosis by TNF family of receptors
TNF
Cell death (apoptosis)
Cell survival ( NFkB)
Tumor necrosis by Thrombus formation of the Tumor vessels
21. Apoptosis- Examplescontd.. 4. Cytotxic T- cell mediated Apoptosis
FasL ?Fas + FasL ?Caspase activation ?Apoptosis
Granzyme B ( serine protease)
Perforin (Transmembrane pore forming molecule)Perforin (Transmembrane pore forming molecule)
22. Apoptosis Deregulation ?Apoptosis
Neuro degenerative disorders- Spino muscular dystrophies (SMA)
Ischemic injury- MI
Apoptosis of viral infected cells by CTLs
?Apoptosis
Mutations/absence of p53
Hormone dependent Tumors- Breast, Ovary, Prostate
Auto-immune diseases ( Auto-reactive Lymphocytes)
22 Dr.T.Krishna MD, www.mletips.com
23. Examples of cell injury and death 1. Ischemia & Hypoxia
MC type of cell injury in clinical medicine
Ischemic injures faster than hypoxia
Reperfusion injury cell injury following restoration of blood flow to the ischemic cells
Mechanism of cell death predominately necrosis in ischemia ( apoptosis is important in reperfusion injury by reactive free radicals, complements, IgM)
2. Chemicals & drugs
Mechanisms
1. Directly acting on cell structures
Mercuric chloride binds sulfhydral (SH) groups of membranes and proteins
Cyanide binds and inactivates mitochondrial cytochrome oxidase
Anti- neoplastic and antibiotics- act on genetic material & proteins 23 Dr.T.Krishna MD, www.mletips.com
24. Examples of cell injury and death 2. Chemicals & drugs
Mechanisms
i). Directly acting on cell structures
ii). Indirectly acting
Convert into active toxic metabolites by p-450 oxidases
Mechanisms by reactive free radicals
Examples Carbon tetrachloride & Acetaminophen (Tylenol)
Carbon tetrachloride (CCl4) = is converted into CCl3? CCl3 is a free radical ? inhibits apoprotein synthesis ? accumulation of Hepatic Lipoproteins (Fatty Liver) and causes auto oxidation of polyenoic fatty acids of membranes
Acetaminophen (Tylenol) = active toxic metabolites produced in liver ? binds and with reduced glutathione peroxidase (GSH) ; large doses of Tylenol depletes GSH and lead to free radical damage of liver (hepatic failure)
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25. Dr.T.Krishna MD, www.mletips.com 25