Stereology-mediated cell count using StereoInvestigator

mariangela.massarocenere

Published: 2024-01-31 DOI: 10.17504/protocols.io.dm6gp3kddvzp/v1

Abstract

Protocol for cell counting using StereoInvestigator software.

Steps

1.

Set slide properly on the microscope and set new reference point

2.

Click on Probes → Optical Fractionator Workflow → Start a new subject →

3.

Enter cut thickness: 30 µm (cut with cryostat)

4.

Enter interval according to the thickness: 5 if SNpc, 6 if STR

5.

In Select Low Mag Lens, click 5X

5.1.

Click on Next Step

6.

Select the Contour of Interest(s)

7.

In Select High Mag Lens select 40X

7.1.

Click on Next Step

8.

In Manually enter the average mounted thickness enter the corresponding one

8.1.

Click on Next Step

9.

In Define the Counting frame enter: 80 x 80 µm

9.1.

Click on Next Step

10.

Enter 25 Percentage

10.1.

Click on Display Changes

11.

Enter: 240x200 µm if SNpc, 620 x 490 µm if STR

11.1.

Click on Display Changes

11.2.

Click on Next Step

12.

In Optical Disector Height enter: 5 µm, 20 µm

12.1.

Click on Next Step

13.

Select your first section

13.1.

Click on Yes

14.

Select the desired region

14.1.

Click on start counting

15.

Focus on the tissue

15.1.

Click on OK

16.

Select a number of markers according to the desired cell types

Note
IMPORTANT 1: Count only the cells with visible nucleus within the squareIMPORTANT 2: If a cell touches a line of the counting frame: if it touches the green line, count the cell; if it touches a red line, do not count it.

17.

Count every defined region from every set section

17.1.

Click on Next Step

17.2.

Click on Display Probe Run List

18.

Click on Section Name → Click on Counter/Marker Name → Select all sections belonging to the same region

19.

Click on View Results

Note
IMPORTANT: Verify that interval corresponds to the interval set in Step 3

20.

Click on the different markers to see the number of cells counted and the estimated cell number

20.1.

Click on CE Scheaffer to view the area if needed

20.2.

Repeat steps 17 through 20.1 for each region

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