L.16 Histology Flashcards

1
Q

L.O.

A
  • Understand the difference between histology and pathology
  • Describe the steps involved in tissue processing for microscopy
  • Compare magnification to resolution
  • Distinguish different nuclei shapes and explain how this can be used to determine cell shape
  • Identify and describe the Haematoxylin and Eosin stain in images
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2
Q

Histology

A

Study of bodys cells and tissues and how they are organised into organs

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3
Q

Pathology

A

Study of adnormal or diseased tissue

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4
Q

Steps involved in tissue processing

A
  1. Specimen aquisition (fresh tissue)
  2. Fixation (preserve structure)
  3. Dehydration (remove water)
  4. Embedding (stiffen to cut, wax, freeze, resin)
  5. Section (improves resolution)
  6. Stain ( produces contrast and specific structure identification)
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5
Q

Magnification

A

Process of enlarging the size of an object through opticl instruments

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6
Q

Resolution

A
  • The ability to distinguish between 2 closely spaced objects/ details in image
  • Smallest distance between 2 points where they can still be seen as seperate things
  • Low resolution = blurry and less distinct features
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7
Q

Light Microscopy:
- Resolving power
- Max magnification
- Section thickness

A
  • Resolving power = 0.2um - 200nm
  • Max magnification = 2000x
  • Section thickness = 5um - 10um
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8
Q

Electron Microscopy:
- Resolving power
- Max magnification
- Section thickness

A
  • Resolving power = 3nm
  • Max magnification = 500,000x
  • Section thickness = 0.025um
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9
Q

Nucleus under microscope

A
  • Shape of nucleus often dictates the shape of a cell
  • Cell mimics the shape of the nucleus
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10
Q

Haematoxylin and Eosin stains

A

Haematoxylin stains:
- Purple = nucleus
- Pink = cytoplasm

Eosin stains:
- Collagen and cytoplasm = shades of pink

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11
Q

4x objective lens magnification

A
  • General microscopy of the tissue
  • Numerous structures
  • Not much detail
  • Cannot identify neclei and indicidual cells
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12
Q

10x objective lens magnification

A
  • Detail improves identify nuclei
  • Cell boarders still indistinguishable
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13
Q

20x objective lens magnification

A
  • Can see shapes of nuclei and cells
  • Stain characteristics are obvious
  • Fewer structures in FOV
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14
Q

40x objective lens magnification

A
  • See inside nuclei
  • Base membrane of cells can be seen
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15
Q

Transmission electron microscopy

A
  • Up to 500,000x magnification
  • See inside cells and resolve things 3nm apart
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