Stereology-mediated cell count using StereoInvestigator
mariangela.massarocenere
Abstract
Protocol for cell counting using StereoInvestigator software.
Steps
Set slide properly on the microscope and set new reference point
Click on Probes → Optical Fractionator Workflow → Start a new subject →
Enter cut thickness: 30 µm (cut with cryostat)
Enter interval according to the thickness: 5 if SNpc, 6 if STR
In Select Low Mag Lens, click 5X
Click on Next Step
Select the Contour of Interest(s)
In Select High Mag Lens select 40X
Click on Next Step
In Manually enter the average mounted thickness enter the corresponding one
Click on Next Step
In Define the Counting frame enter: 80 x 80 µm
Click on Next Step
Enter 25 Percentage
Click on Display Changes
Enter: 240x200 µm if SNpc, 620 x 490 µm if STR
Click on Display Changes
Click on Next Step
In Optical Disector Height enter: 5 µm, 20 µm
Click on Next Step
Select your first section
Click on Yes
Select the desired region
Click on start counting
Focus on the tissue
Click on OK
Select a number of markers according to the desired cell types
Count every defined region from every set section
Click on Next Step
Click on Display Probe Run List
Click on Section Name → Click on Counter/Marker Name → Select all sections belonging to the same region
Click on View Results
Click on the different markers to see the number of cells counted and the estimated cell number
Click on CE Scheaffer to view the area if needed
Repeat steps 17 through 20.1 for each region