1. PATHOLOGY PHT218 Unit 3 CELL INJURY & CELL DEATH

2. Overview of Cellular Injury
Cells actively control the composition of their immediate environment and intracellular surrounding within a narrow range of physiological parameters (“homeostasis”)
Under physiological stresses or pathological stimuli (“injury”), cells can undergo adaptation to achieve a new steady state that would be compatible with their viability in the new environment.
Cellular injury may be a reversible process, in which case the cells can recover their normal function, or it may be irreversible and lead to cell death and necrosis
If the injury is too severe (“irreversible injury”), the affected cells die.

3. Overview of Cellular Injury

5. Reversible and Irreversible Cell Injury

6. Outcomes from cell injury depend upon:
Type of injury
Severity of the injury
Duration of the injury
Type of cell being injured-Some cell types sustain injury better than others; some tissues (e.g. liver) have a capacity to regenerate.

7. Causes of Cellular Injury (أسباب الإصابة الخلوية)
Hypoxia (oxygen deficiency) and ischemia (blood flow deficiency)
Physical injury
Mechanical trauma
Temperature extremes (burn injury, frostbite )
Electrical current
Chemical injury
Chemicals, toxins, heavy metals, solvents, smoke,
pollutants, drugs, gases
Radiation injury
Ionizing radiation — gamma rays, X rays
Non-ionizing radiation — microwaves, infrared, laser
Biologic agents
Bacteria, viruses, parasites
Nutritional injury
Malnutrition: Protein deficiency
Over nutrition: Obesity

8. More Energy
Ionizing Radiation
Less Energy
Non -ionizing Radiation

9. Mechanisms of Cellular Injury
Although the causes of cellular injury are many, the underlying mechanisms of cellular injury usually fall into one of two categories:
Uncontrolled free radical injury
hypoxic injury (impaired oxygen delivery or utilization) .

10. Primary Site of Impact
1) Oxidative phosphorylation ‑ ATP generation
2) Membrane integrity ‑ osmotic pump
3) Protein synthesis ‑ cell repair
4) Nuclear integrity ‑ direction of cell functions

11. Free Radical Injury
Free radicals are highly reactive chemical species that have one or more unpaired electrons in their outer shell.
Examples of free radicals include superoxide (O2−), hydroxyl radicals (OH−) and hydrogen peroxide (H2O2).
Free radicals are generated as by-products of normal cell metabolism and are inactivated by free radical–scavenging enzymes within the body such as catalase and glutathione peroxidase
When excess free radicals are formed from exogenous sources or the free radical protective mechanisms fail, injury to cells can occur.

12. Oxygen molecule and generation of free radical

13. Free Radical Injury
Free radicals are highly reactive and can injure cells through:
1. Peroxidation of membrane lipids
2. Damage of cellular proteins
3. Mutation of cellular DNA
Exogenous sources of free radicals include tobacco smoke, organic solvents, pollutants, radiation and pesticides.
Free radical injury has been implicated as playing a key role in the normal aging process as well as in a number of disease states such as diabetes mellitus, cancer, atheroscelrosis, Alzheimer’s disease and rheumatoid arthritis.

14. Effects of free radical cell injury

15. Hypoxic Cell Injury
Hypoxia is a lack of oxygen in cells and tissues that generally results from ischemia.
During periods of hypoxia, aerobic metabolism of the cells begins to fail.
This loss of aerobic metabolism leads to dramatic decreases in energy production (ATP) within the cells. Hypoxic cells begin to swell as energy-driven processes (such as ATP-driven ion pumps) begin to fail.
The pH of the extracellular environment begins to decrease as waste products (such as lactic acid, a product of anaerobic metabolism) begin to accumulate.

16. Hypoxic Cell Injury
The cellular injury process may be reversible, if oxygen is quickly restored, or irreversible and lead to cell death.
Certain tissues such as the brain are particularly sensitive to hypoxic injury. Death of brain tissues can occur only 4 to 6 minutes after hypoxia begins.
The loss of ionic balance in hypoxic cells can also lead to the accumulation of intracellular calcium, which is normally closely regulated within cells.
There are a number of calcium-dependent protease enzymes present within cells that become activated in the presence of excess calcium and begin to digest important cellular constituents.

17. Unit 3 Objectives
Define homeostasis of cells?
Write the types of cell injury?
Write the characteristics of reversible injury?
Write the characteristics of irreversible injury?
Write the factors on which the outcome of disease depends on?
Define the different cause or etiology of disease?
Name the 2 main mechanisms of cellular injury?
What are free radicals? Name the free radicals found in the body?
Name the free radical scavenging enzyme?
How does the free radical bring about cell injury?
Name the important disease caused as a result of free radical injury?
Write the mechanism of hypoxic cell injury?
What happens when there is loss of ionic balance in hypoxic cells?

18. Cell Death

19. Like disease, cell death may be caused by
internal (intrinsic) factors that limit the cell's life span or
external (extrinsic) factors that contribute to cell damage and aging.
When a stressor is severe or prolonged, the cell can no longer adapt and it dies.
Cell death, or necrosis, may manifest in different ways, depending on the tissues or organs involved.

20. Cell Death

21. Apoptosis :Individual Cell Death
Apoptosis is genetically programmed cell death.
common event in some regenerating tissues: such as skin and gut epithelium and during embryogenesis
Not a typical event in developed tissues such as brain
Becomes a serious occurrence when many cells are involved in such organs as the liver

22. Examples of Physiologic Apoptosis
(A) separation of webbed fingers and toes in embryo,
(B) development of neural connections,
(C) removal of cells from intestinal villa, and
(D) removal of senescent (old) blood cells.

23. Examples of Pathologic Apoptosis
Irradiated tissues
Viral infections e.g. Viral Hepatitis
Hormone-dependent atrophy of tissue (e.g., endometrial cell breakdown after withdrawal of estrogen and progesterone in the menstrual cycle)
Death of tumor cells by cytotoxic T cells

24. Liquefactive necrosis: in brain,
Types of Necrosis
Liquefactive necrosis: in brain,
Caseous necrosis: Infection with Mycobacterium tuberculosis
Fat necrosis: Liver and pancreas
Coagulative necrosis: Necrosis of kidney, liver, or heart muscle
Gangrene: Necrosis of an appendage, usually limbs

25. occurs when a lytic (dissolving) enzyme liquefies necrotic cells.
Necrosis
Liquefactive necrosis
occurs when a lytic (dissolving) enzyme liquefies necrotic cells.
It is generally associated with abscess formation
Typically, liquefaction necrosis occurs in brain infarcts and pancreatic necrosis.
Liquefaction by leukocytic enzymes is called suppuration, and the resultant fluid is called pus.

26. Liquefactive necrosis (brain abscess), ovine6
Liquefactive necrosis (brain abscess), ovine

27. 2. In caseous necrosis,
the necrotic cells disintegrate but the cellular pieces remain undigested for months or years.
*This type of necrotic tissue gets its name from its crumbly, cheese- like (caseous) appearance.
It commonly occurs in lung tuberculosis.

28. caseous necrosis

29. The tissue becomes opaque and chalky white.
Necrosis
3. In fat necrosis,
*enzymes called lipases break down intracellular triglycerides into free fatty acids.
These free fatty acids combine with sodium, magnesium, or calcium ions to form soaps.
The tissue becomes opaque and chalky white.
It is characteristic of tissues adjacent to pancreatic necrosis.

30. *It typically affects the kidneys, heart, and adrenal glands.
4. Coagulative necrosis
*is the most common form of necrosis in cells without large numbers of lysosomes.
*Commonly occurs when the blood supply to any organ (except the brain) is interrupted (ischemia).
*It typically affects the kidneys, heart, and adrenal glands.
Lytic (lysosomal) enzyme activity in the cells is inhibited, so that the necrotic cells maintain their shape, at least temporarily.

31. fat necrosis
Coagulative
Necrosis in liver

32. Coagulative necrosis

33. Necrosis
5- Gangrenous necrosis,
a form of coagulative necrosis, typically results from a lack of blood flow and is complicated by an overgrowth and invasion of bacteria.
It commonly occurs in the lower legs as a result of arteriosclerosis or in the gastrointestinal tract( GIT).

34. Necrosis
Gangrene can occur in one of three forms: dry, moist (or wet), or gas.
Dry gangrene occurs when bacterial invasion is minimal. It's marked by dry, wrinkled, dark brown or blackened tissue on an extremity.
Moist (or wet) gangrene develops with liquifactive necrosis that includes extensive lytic activity from bacteria and white blood cells to produce a liquid center in an area of tissue. It can occur in the internal organs as well as the extremities.
Gas gangrene develops when anaerobic bacteria of the genus Clostridium infect tissue. It's more likely to occur with severe trauma and may be fatal. The bacteria release toxins that kill nearby cells and the gas gangrene rapidly spreads. Release of gas bubbles from affected muscle cells indicates that gas gangrene is present.

35. Cell Death

36. Difference between Apoptosis & Necrosis
Regulation
Genetic programmed
Ischemia, trauma or ATP depletion
Control
Controlled
Uncontrolled
Cell shape
Skrinkage, condensed
Swelling
Plasma membrane integrity
Maintained
Collasped
Cellular process
Budding
Blebbing
Cellular content
Packaged in apoptoic bodies
Leakage to extracellular fluid
DNA
Fragmentation, chromatin condensation
No fragmentation
Energy
ATP required
Not required
Inflammatory response
Absent
Present
Mediator
Caspase
Caspase-independent
فقاعة

37. Pathology of Necrosis OR Necrotic Changes
When a cell dies, enzymes inside the cell are released and start to dissolve cellular components. This triggers an acute inflammatory reaction in which white blood cells migrate to the necrotic area and begin to digest the dead cells. At this point, the dead cells — primarily the nuclei — begin to change morphologically in one of three ways:
Pyknosis, in which the nucleus shrinks, becoming a dense mass of genetic material with an irregular outline.
Karyorrhexis, in which the nucleus breaks up, strewing pieces of genetic material throughout the cell.
Karyolysis, in which hydrolytic enzymes released from intracellular structures called lysosomes simply dissolve the nucleus.

38. Necrotic Changes

39. Enzyme Markers of Cell Death

40. Unit 3 Objectives
Define apoptosis?
Give examples of physiological apoptosis?
Give examples of pathological apoptosis?
Name the types of Necrosis and the organs affected by them?
What is liquefactive necrosis?
Which type of necrosis is associated with abscess formation?
Where would you find liquefactive necrosis?
What is caseous necrosis?
Which type of necrosis there cheese like appearance?
Define fat necrosis?
In which type of necrosis the tissue becomes chalky white?
Which is the most common form of necrosis?

41. Unit 3 Objectives
In which type of cells would you find fat necrosis?
Define coagulative necrosis?
What is gangrenous necrosis?
Define the 3 forms of gangrene?
Write the difference between apoptosis and necrosis?
Write about the necrotic changes in the nucleus?
What is pyknosis, karyolysis, and karyorrhexis
Name the Enzyme Markers of Cell Death?