L.16 Histology Flashcards
L.O.
- 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
Histology
Study of bodys cells and tissues and how they are organised into organs
Pathology
Study of adnormal or diseased tissue
Steps involved in tissue processing
- Specimen aquisition (fresh tissue)
- Fixation (preserve structure)
- Dehydration (remove water)
- Embedding (stiffen to cut, wax, freeze, resin)
- Section (improves resolution)
- Stain ( produces contrast and specific structure identification)
Magnification
Process of enlarging the size of an object through opticl instruments
Resolution
- 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
Light Microscopy:
- Resolving power
- Max magnification
- Section thickness
- Resolving power = 0.2um - 200nm
- Max magnification = 2000x
- Section thickness = 5um - 10um
Electron Microscopy:
- Resolving power
- Max magnification
- Section thickness
- Resolving power = 3nm
- Max magnification = 500,000x
- Section thickness = 0.025um
Nucleus under microscope
- Shape of nucleus often dictates the shape of a cell
- Cell mimics the shape of the nucleus
Haematoxylin and Eosin stains
Haematoxylin stains:
- Purple = nucleus
- Pink = cytoplasm
Eosin stains:
- Collagen and cytoplasm = shades of pink
4x objective lens magnification
- General microscopy of the tissue
- Numerous structures
- Not much detail
- Cannot identify neclei and indicidual cells
10x objective lens magnification
- Detail improves identify nuclei
- Cell boarders still indistinguishable
20x objective lens magnification
- Can see shapes of nuclei and cells
- Stain characteristics are obvious
- Fewer structures in FOV
40x objective lens magnification
- See inside nuclei
- Base membrane of cells can be seen
Transmission electron microscopy
- Up to 500,000x magnification
- See inside cells and resolve things 3nm apart