Cellular Adaptations Flashcards

1
Q

____ involves gene activation, protein synthesis and production of organelles

A

hypertrophy involves gene activation, protein synthesis and production of organelles

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2
Q

permanent tissues (e.g. ____) cannot make new cells and undergo ___ only

A

permanent tissues (e.g. cardiac muscle, neurons, skeletal muscle) cannot make new cells and undergo hypertrophy only

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3
Q

describe the process of atrophy

A
  • decrease in cell size occurs via ubiquitin-proteosome degradation of the cytoskeleton and autophagy of cellular components
    • in ubiquitin-proteosome degradation, intermediate filaments of the cytoskeleton are tagged with ubiquitin and destroyed by proteosomes
    • autophagy of cellular components involve generation of autophagic vacuoles
      • these vacuoles fuse with lysosomes whose hydrolytic enzymes breakdown cellular components
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4
Q

describe 3 possible causes of atrophy

A
  • decrease in size and function of cell due to:
    • decreased workload and/or blood supply
    • loss of innervation or aging
    • loss of trophic signals (loss of endocrine stimulation)
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5
Q

name 3 potential causes of hyperplasia

A
  • increase in the number of cells due to:
    • increased functional demand
    • hormonal stimulation
    • persistent injury
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6
Q

describe metaplasia

A
  • a change in stress of an organ leads to a change in cell type (by genetic reprogramming of stem cells)
    • most commonly involves change of one type of surface epithelium (squamous, columnar or urothelial) to another
    • metaplastic cells are better able to handle the new stress
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7
Q

describe Barrett esophagus

A
  • esophagus is normally lined by nonkeratinizing squamous epithelium (suited to handle friction of food bolus)
  • acid reflux from the stomach causes metaplasia to nonciliated, mucin-producing columnar cells (better able to handle stress of acid)
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8
Q

describe what is seen in the image

A
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9
Q

metaplasia occurs via reprogramming of _____

A

metaplasia occurs via reprogramming of stem cells, which then produce the new cell type

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10
Q

under persistent stress, metaplasia can progress to ____ and eventually result in ____

name an example and an exception

A

under persistent stress, metaplasia can progress to dysplasia and eventually result in cancer

  • Barrett esophagus may progress to adenocarcinoma of the esophagus
  • a notable exception is apocrine metaplasia of breast, which carries no increased risk for cancer
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11
Q

____ deficiency can result in metaplasia

explain why

A

vit. A/retinoic acid deficiency can result in metaplasia

  • vit. A is necessary for differentiation of specialized epithelial surfaces such as the conjunctiva covering the eye
  • in vit. A deficiency, the thin squamous lining of the conjunctiva undergoes metaplasia into stratified keratinizing squamous epithelium
    • this change is called keratomalacia
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12
Q

describe what is seen in the image

A

keratomalacia ; caused by vit. A deficiency, which results in an inability to maintain the highly specialized surface that covers the eye

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13
Q

describe dysplasia

A

disordered cellular growth

  • refers to the proliferation of precancerous cells
  • enlarged, irregular, dark nuclei
  • often arises from longstanding pathologic hyperplasia (endometrial hyperplasia) or metaplasia (Barrett esophagus)
  • dysplasia is reversible with alleviation of inciting stress
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14
Q

if stress persists, dysplasia progresses to ____ which is _____

A

if stress persists, dysplasia progresses to carcinoma which is irreversible

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15
Q

describe aplasia and name an example

A
  • aplasia is failure of cell production during embryogenesis (e.g. unilateral renal agenesis)
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16
Q

describe hypoplasia

A
  • hypoplasia is a decrease in cell production during embryogenesis, resulting in relatively small organs (e.g. streak ovary in Turner syndrome)