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Adipocytes Tools
The Adipocytes Tools help to analyze fat cells in images from histological sections such as this one: example image.
The source code in git-hub can be found here.
To install the tools, drag the link Adipocyte_Tools.ijm to the ImageJ launcher window and save it under macros/toolsets in the ImageJ installation. In order to use the greyscale-watershed method (the w-button) you must have the Watershed Algorithm installed.
Select the "MRI Adipocytes Tools" toolset from the >> button of the ImageJ launcher.
- the first button (the one with the image) opens this help page
- the p button runs a preprocessing step that clears the background of the image
- the s button runs a simple segmentation algorithm on the current image
- the w button runs a greyscale-watershed segmentation on the current image
- the l button runs a segmentation for large-magnification images on the current image
Open an image and press the p button. After a moment of calculation the background should become black. This preprocessing is used in the two segmentation methods when "watershed" is used. Without it the watershed-algorithm would split the background into objects as well. A right click on the p button opens the options dialog.
- min. size is the minimum size a cell must have to be taken into account
- max. size is the maximum size a cell can have to be taken into account
- nr. of dilations : to determine the background first the objects are detected. Since the objects are not connected dilate is called the given number of times to connect them
- thresholding method the thresholding method used to segment the objects.
You can run this method by pressing the s button. The simple segmentation will basically run "find edges" and invert the contrast so that cells and the background become clear and membranes dark. Then an automatic threshold is applied and the particle analyzer is used to detect the cells. Cells touching the edges of the image are excluded, since they would falsify the mean area measurements. You will find that often multiple cells appear connected and are counted as one. You can decide to use a binary watershed with this method to get better results. In this case the background is first cleared as in the preprocessing above.
A right click on the s button opens the options dialog. In addition to the options of the preprocessing a "use binary watershed" checkbox can be selected or deselected.
- You can exclude regions from the analysis by making a selection and calling Edit>Clear from ImageJ (supposed that the background color is black).
- You can select a detected cell by clicking on its label in the image. This will select the cell in the roi-manager as well.
- To delete a cell, select it and press the Delete button on the roi-manager
- To add a cell, select the freehand-selection tool, draw the contour of the cell and press Add on the roi-manager
- To merge two cells, click on the label of the first cell. Search the index of the second cell in the list in the roi-manager and click on it with Ctrl held down. Click on More>OR (Combine). Now press Delete to remove the old cells. Use the freehand selection tool while holding down Shift to fill the gap between the two parts of the selection that is still on the image and press Add.
- To split a cell into two, select it by clicking on its label in the image. Press Delete on the roi manager. Use the freehand selection tool with the Alt key held down to draw a separation. Click on More>Split on the roi-manager.
- Make sure that under Analyze>Set Measurements Area is selected. Press the measure button on the roi-manager. Be careful running the macro a second time will delete the results table. You can copy and paste the content into a spreadsheet application.
- Options that you set remain valid until you change the current toolset or until you close ImageJ. After that the default-options well be active.
- If you select the toolset with Shift held down, the toolset will be opened in a text-editor you can change the default values for the options and save the file.
You can run this method by pressing the w button. A greyscale watershed algorithm is used to separate touching cells. Before the application of the watershed a Gaussian-blur filter is used to smooth the image and to avoid over-segmentation. In the options the additional option sigma for the size of the Gaussian-blur filter must be supplied. The hints in the last section apply for this method as well.
In this case the whole image should be filled with adipocytes. The background intensity across the image risks to be not homogene (i.e. higher in the middle and lower at the borders). Therefore the Fit Polynomial plugin is used to homogenize it. After thresholding the image is eroded to connect the cell membranes. Fill holes is used to get rid of the spots created in this process.
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AdipoQ - A simple toolbox of two ImageJ plugins for quantifying adipocyte morphology and function in tissues and in vitro.
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Palomäki, V.A., Koivukangas, V., Meriläinen, S., Lehenkari, P., Karttunen, T.J., 2022. A Straightforward Method for Adipocyte Size and Count Analysis Using Open-source Software QuPath. Adipocyte 11, 99–107. https://doi.org/10.1080/21623945.2022.2027610 - A method to measure adipocytes using QuPath's pixel classifiers, check this out, especially if you are working on whole slide images.
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Zhi, X., Wang, J., Lu, P., Jia, J., Shen, H.-B., and Ning, G. (2018). AdipoCount: A New Software for Automatic Adipocyte Counting. Frontiers in Physiology 9.
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