University:
Kentucky State University
Course:
BIO 408 | Cell Biology
Academic year:

2024
Views:

364

Pages:

30
Author:

Caroline Mcfarland

Introduction to pathology lecture 5/ Cell injury apoptosis Apoptosis = programmed cell death = cell suicide= individual cell death Apoptosis • cell death induced by a tightly regulated suicide program in which cells activate enzymes capable of degrading the cells' own nuclear DNA and nuclear and cytoplasmic proteins. • Fragments of the apoptotic cells break off, giving the appearance that is responsible for the name (apoptosis, "falling off"). apoptosis • The plasma membrane remains intact. • Apoptotic bodies (contain portions of the cytoplasm and nucleus) become targets for phagocytosis before their contents leak out and so there would be no inflammatory reaction. • So in apoptosis there is no damade to surrounding cells. Causes of Apoptosis • Physiologic situations: To eliminate cells that are no longer needed OR to maintain a steady number of various cell populations in tissues. Physiologic apoptosis • Embryogenesis. • involution of hormone-dependent tissues upon hormone withdrawal. (endometrium and breast after pregnancy) • Cell loss in proliferating cell populations. (gastrointestinal tract, skin…) • Death of host cells after serving their useful function. (neutrophils and lymphocytes in inflammation) • Elimination of potentially harmful self-reactive lymphocytes. • Cell death induced by cytotoxic T lymphocytes (tumor cells and virally infected cells) Pathologic situations • DNA damaged cells, if DNA damage is severe and cannot be repaired the cell dies by apoptosis. • Cells with accumulation of misfolded proteins, • Certain infections (viral ones): may be induced by the virus (as in human immunodeficiency virus infections) or by the host immune response (as in viral hepatitis). • Pathologic atrophy in parenchymal organs after duct obstruction (pancreas, parotid and kidney) Morphology • Cell shrinkage: dense cytoplasm, tightly packed organelles. • Chromatin condensation: peripherally under the nuclear membrane. • Formation of cytoplasmic blebs • apoptotic bodies: blebbing then fragmentation into membrane bound apoptotic bodies composed of cytoplasm and tightly packed organelles with or without nuclear fragments. Morphology • Phagocytosis of apoptotic cells or cell bodies by macrophages (quickly hence no inflammation). Mechanisms of Apoptosis • Activation of enzymes called caspases . • Two main pathways: • 1- Mitochondrial pathway (intrinsic) • 2- Death receptor pathway (extrinsic) • 1- mitochondrial pathway (intrinsic) • Leak of cytochrome c out of mitochondria and activation of caspase 9… • 2- death receptor pathway (extrinsic) • Involved in elimination of self-reactive lymphocytes and in killing of target cells by some cytotoxic T lymphocytes. • Activation of caspase 8. Intrinsic pathway = mitochondrial pathway • Mitochondria contains several proteins that can induce apoptosis • The most important of these is cytochrome C • Stimulation of apoptosis depends on mitochondrial permeability • Mitochondrial permeability is controlled by a family of more than 20 proteins ( Bcl2 family) • When cells are deprived of growth signals, or exposed to severe DNA damage or have misfolded proteins.. In all these situations certain sensors are activated • These sensors are called BH3 proteins ( they are part of the bcl2 family) • BH3 now activate proapoptotic members of the family= Bax and Bak • When bax and bak are stimulated they dimerize and insert into the mitochondrial membrane • They form channels through which cytochrome c escapes into cytosol • BH3 also inhibit anti inhibitory members of the family (BCL-2 and BCL-xl) • So BH3 stimulate proapptotic and inhibit antiapoptotic signals.. Net result it leakage of cytochrome c from the mitochondria to cytosol • Once cytochrome c is in the cytosol it stimulates caspase 9 • Caspase cascade is stimulated leading to nuclear fragmentation by executioner caspases. Summary of intrinsic pathway • BH3 stimulates pro-apoptotic (bax, bak), and inhibit anti apoptotic proteins (bcl-2, bcl-xl) • Cytochrome c leaks out • Stimulates caspase 9 • Stimulates executioner caspases that degrade cell components Extrinsic pathway= death receptor pathway • This pathway is triggered by death receptors, which are members of the TNF ( tumor necrosis factor) receptor family • The most important types of death receptors are: TNF type 1 receptor and Fas receptor (CD95) • FasL = fas ligand is a membrane protein expressed mainly on T lymphocytes • When T cells recognize fas expressing target , fas molecules are cross linked by fasl to activate caspase 8 • Caspase 8 activates executioner caspases that degrade cell components FLIP • FLIP is a protein that is a Caspase antagonist which block activation of caspases.. So it inhibit apoptosis. • Some viruses produce FLIP like molecule to keep infected cells alive.( so the virus can survive within that cell) Clearance of apoptotic cells • When apoptotic cells fragment they are phagocytosed without eliciting inflammation • In normal cells phosphatidyl serine is present in the inner surface of cell membrane.in apoptotic cells it flips to outside the membrane and acts as a signal recognized by macrophages to phagocytose the apoptotic cell fragment • So the apoptotic body is phagocytosed without inflammation note • In some situations both apoptosis and necrosis occur • necroptosis P53 and apoptosis • DNA damage causes accumulation of p53 in cells • It arrests cells in G1 phase of cell cycle to give the cell a chance to repair itself • If no repair, p53 triggers apoptosis by stimulating bax and bak • P53 can be mutated in cancer cells.. If mutated it cannot initiate apoptosis, so the cell survives even if its DNA is damaged.. Longer survival of a cell with damaged DNA increases the chances of accumulating more mutations.. So this cell can become malignant Accumulation of abnormal proteins ER ( endoplasmic reticulum) stress • Chaperons in ER control proper folding of proteins • Misfolded proteins are degraded. • If there is too much of unfolded protein.. Then the cell starts an unfolded protein response which is an adaptive response aiming at increasing chaperons and decreasing protein translation • If more unfolded proteins accumulate : the situation is called ER stress. • ER stress causes caspase activation and apoptosis. Feature Necrosis Apoptosis Cell size Enlarged (swelling) Reduced (shrinkage) Nucleus Pyknosis → karyorrhexis → karyolysis Fragmentation into nucleosome-size fragments Plasma membrane Disrupted Intact; altered structure, especially orientation of lipids Cellular content Enzymatic digestion; may leak out of cell Intact; altered structure, especially orientation of lipids Adjacent inflammation Frequent No Physiologic or pathologic role Invariably pathologic (culmination of irreversible cell injury) Often physiologic, means of eliminating unwanted cells; may be pathologic after some forms of cell injury, especially DNA damage

Cell Injury Apoptosis

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