Lecture 25: Cell Adaptation Flashcards

1
Q

Cells responses to stress and injury

A

1) Physiological response
- Adaptation to a stimulus within the normal range

2) Pathological responses:
- Adaptation to a stimulus outside normal range
- Can result in cell malfunction, damage, death

  • Response depends on
    1) Stimulus
    2) Duration
    3) Magnitude
    4) Vulnerability
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2
Q

Cause of cell injury

A

1) Metabolic
- Hypoxia= Oxygen deficiency
- Ischemia= blood flow deficiency
- Nutritional= def or excess

2) Chemical
- Ex: Drugs/alch

3) Physical
- Trauma
- Extreme tempts
- Radiation

4) Biological
- Virus/bacteria, parasite

5) Immunological
- Allergic rxns
- Autoimmune disease

6) Genetic
- Chromosomal abnormalities
- Mutations

7) Aging
- Cell aging (senescence)

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3
Q

Major intracellular systems affected when cell injury occurs

A

1) Membrane integrity
2) ATP Production
3) Protein synthesis
4) Genomic or chromosomal integrity

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4
Q

Intracellular systems affects by cell injury (More important)

A

1) Membrane integrity (Damage)
- Plasma membrane
- Organelles

2) ATP Production
3) Protein synthesis
4) Genomic or chromosomal integrity

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5
Q

Kinds of injury

  • Reversible
  • Irreversible
A

Reversible= mild, can recover/regain function

Irreversible= severe

  • Membrane damage
  • DNA damage
  • Cell death (Necrosis/apoptosis)
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6
Q

Early cellular response to injury

A
  • Mild damage to cell
  • Cell degeneration
  • Reversible

1) Cloudy swelling (pale staining, due to swelling of organelles)
2) Hydropic degeneration (Swelling continued, vacuoles appear in cytoplasm)

3) Fatty Change (accumulation of triglycerides in cytoplasm)
- most common in liver
- common cause= toxins/alch

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7
Q

Cell adaptation to Nonlethal injury:

1) Atrophy
2) Hypertrophy
3) Hyperplasia
4) Metaplasia

A

1) Atrophy- Decreased size/function in cell
- Ex: Losing weight
- Reversible
- Causes: Decreased functional demand, decreased blood supply, loss innervation, loss of endocrine stimulation, nutritional deficient, aging
- Common tissues effected:
1) Testis (elderly)
2) Skeletal muscle
3) Brain (Neurodegenerative/aging)

2) Hypertrophy- Increase in size of cell
- Ex: gaining weight
- Cells never increase in #
- Can increase organ size
- reversible
- Cause: hormone, increased functional demand (bigger muscles to lift more weight)
- Common tissues effected:
1) cardiac muscles (only thing that can affect cardiac muscles)
2) Skeletal muscles
3) Uterus (pregnancy)

3) Hyperplaisa- Increase in number of cells
- reversible
- Cause: hormone, increased functional demand
- Common tissues effected:
1) Endometrium
2) Prostate gland
3) RBC
4) Glandular Epithelium of breast
5) Uterine enlargement

4) Metaplaisia- Change in differentiation
- Ex: Cancer, esophagus: stratified squamous epithelium transforms to stratified squamous epithelium
- Reversible
- One cell type is replaced by another cell type
- Cause: Adaptive response to environmental stimuli (Ex: cigs smoke, acid reflux)
- Common tissues effected:
1) Respiratory epithelium
2) Cervical epithelium
3) Esophageal epethelium
- Increased risk for dyplasia and neoplasia

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8
Q

Atherosclerosis

A

Narrowing of renal artery (Kidney atrophy)

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9
Q

Atherosclerotic Cerebrovascular disease

A

brain atrophy (eldery male)

Can see by bigger spacing in between fissures

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10
Q

Involution

A
  • Organ shrinks/returns to normal

- Usually occurs after stimulus is removed

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11
Q

Dyplasia

A
  • Failure of differentiation and maturation
    1) Cellular atypia
  • Structurally abnormal
  • High nuclear to cytoplasm ratio (More nuclei)
  • Large nuclei with darker staining chromosome

Cause:

  • Rapid multipication of cells
  • May demonstrate genetic abnormalities

Tissues commonly affected:

  • cervix
  • skin
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12
Q

Neoplasia

A
  • Abnormal mass of cells
  • Cellular proliferation and growth in the absence of an eternal stimulus
  • Variable states of differentiation
  • 2 main groups
    1) Benign
    2) Malignant
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13
Q

Carcinoma in situ

A

-Features of carcinoma without breach of basement membrane:

  • Structural abnormalities
  • Cell Crowding
  • Pleomorphisms
  • increased and abnormal mitotic activity
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