Sean Lauber:Differential cell staining: Difference between revisions
(New page: To differentially stain the cytocentrifuge smears (from BAL), the Hema3 reagent is used (Fisher, 23-123-869). Protocol for staining (each dip is done for 1 second): 1. Dip one slide...) |
No edit summary |
||
| Line 1: | Line 1: | ||
To differentially stain the cytocentrifuge smears (from BAL), the Hema3 reagent is used (Fisher, 23-123-869). | To differentially stain the cytocentrifuge smears (from BAL), the Hema3 reagent is used (Fisher, 23-123-869). | ||
== Protocol for staining (each dip is done for 1 second): == | |||
1. Dip one slide into the fixative (clearish blue) 5times. | 1. Dip one slide into the fixative (clearish blue) 5times. | ||
| Line 24: | Line 26: | ||
== Differential counting == | |||
Count up to 500 cells for each cytocentrifuge smear and classify each cell as either a macrophage/monocyte, lymphocyte, neutrophil or eosinophil. Then calculate the % for each from the total. Then you can apply the % to the total cell count to determine the total number of each of these cell types. This will let you know if certain cell types are increased upon treatment. | Count up to 500 cells for each cytocentrifuge smear and classify each cell as either a macrophage/monocyte, lymphocyte, neutrophil or eosinophil. Then calculate the % for each from the total. Then you can apply the % to the total cell count to determine the total number of each of these cell types. This will let you know if certain cell types are increased upon treatment. | ||
Revision as of 11:29, 30 October 2012
To differentially stain the cytocentrifuge smears (from BAL), the Hema3 reagent is used (Fisher, 23-123-869).
Protocol for staining (each dip is done for 1 second):
1. Dip one slide into the fixative (clearish blue) 5times.
2. Drain excess fixative.
3. Dip slide into the Xanthene solution (red) 4 times.
4. Blot onto paper towel.
5. Dip slide into the Thiazine solution (purple) 3 times.
6. Drain excess.
7. Rinse the slide immediately with distilled water.
8. Allow the slide to air dry completely overnight.
9. Mount with Permount or something similar and coverslip.
If a deeper stain is desired, add another dipping step. Remove a step is you want less staining.
Differential counting
Count up to 500 cells for each cytocentrifuge smear and classify each cell as either a macrophage/monocyte, lymphocyte, neutrophil or eosinophil. Then calculate the % for each from the total. Then you can apply the % to the total cell count to determine the total number of each of these cell types. This will let you know if certain cell types are increased upon treatment.
Macrophage/Monocyte: - Large cells; monocytes are smaller - Dark Staining nucleus - Large cytoplasm that staisn clear or light purple; monocytes have a smaller cytoplasm - Frizzled outer membrane (macrophage processes) when activated; Monocytes have a smoother outer membrane - Can have lots of vessicles inside - Sometimes multinucleated (when close to dividing or when recently engulfed a cell)
Lymphocyte (look very similar to monocytes so be careful): - Small cell - Dark staining nucleus - Have very little cytoplasm (a tiny slit) (monocytes tend to have more) that stains clear or light purple - Sometimes all you see is a dark staining nucleus, if you look closely you'll see the membrane containing very little cytoplasm - Can be frizzled
Neutrophil - Small cell - Dark staining, lobulated nucleus - Has little cytoplasm that stains clear or light purple
Eosinophil
- Small cell
- Dark staining, lobulated nucleus
- Has little cytoplasm with granules that stain pink
