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Published on: May 5, 2017
Direct Fast Scarlet and Congo Red Staining in Identification of Eosinophils and Their Cell-Free Granules in Cardiac
Takayuki Kumaki1, Tomoe Abe2,3, Takeshi Kashimura1
1Department of Cardiovascular Medicine, Niigata University Graduate School of Medical and Dental Sciences.
Insights
Direct fast scarlet (DFS) and Congo red (CR) effectively stain cardiac eosinophil granules, outperforming standard haematoxylin-eosin (HE) staining. DFS offers superior specificity and accuracy for diagnosing eosinophil-related heart conditions.
Area of Science:
- Cardiovascular Pathology
- Histopathology
- Immunohistochemistry
Background:
- Cell-free eosinophil granules in cardiac tissue can be difficult to detect with standard haematoxylin-eosin (HE) staining.
- Direct fast scarlet (DFS) and Congo red (CR) are potential alternatives for visualizing eosinophil granules.
- Evidence for DFS and CR efficacy in cardiac eosinophil detection is limited.
Purpose of the Study:
- To confirm DFS and CR staining of cardiac eosinophil granules.
- To evaluate the advantages of DFS and CR over HE for eosinophil detection.
- To assess the utility of DFS and CR in diagnosing eosinophil-related cardiac disorders.
Main Methods:
- Paraffin-embedded endomyocardial biopsy samples from patients with eosinophilic cardiac disorders and lymphocytic myocarditis were used.
- Serial sections were stained with HE, DFS, and CR.
- Immunofluorescence for major basic protein (MBP) and galectin-10 was employed for eosinophil identification.
- ImageJ software was used for quantitative analysis of stained granules.
Main Results:
- DFS and CR staining distributions resembled HE staining, identifying eosinophil granules (MBP-positive) within intact eosinophils (galectin-10-positive).
- Both DFS and CR stained cell-free granules indicative of degranulation (ETosis).
- DFS staining allowed for more specific identification of eosinophil granules compared to HE and CR, with cardiologists counting more eosinophils in DFS-stained sections.
Conclusions:
- Direct fast scarlet (DFS) staining effectively identifies eosinophils and their cell-free granules in cardiac tissues.
- DFS demonstrates superior performance compared to HE and CR for eosinophil detection in cardiac biopsies.
- DFS has the potential to improve the diagnosis and management of eosinophil-related heart diseases.
Abstract:
Cell-free eosinophil granules, harmful to the heart, are stained red by haematoxylin-eosin (HE); however, they can be overlooked in cardiac tissues. Direct fast scarlet (DFS) and Congo red (CR), known for staining amyloids, may offer clearer detection of eosinophil granules; however, no firm evidence exists. This study aimed to confirm that DFS and CR stain eosinophil granules and evaluate their advantages over HE.Paraffin-embedded endomyocardial biopsy samples from 6 patients with eosinophil-infiltrating cardiac disorders and 6 with lymphocytic myocarditis were stained.The distributions of red granules stained with DFS and CR resembled those stained with HE in serial sections. Eosinophil granules, identified by major basic protein (MBP), were detected in intact eosinophils, identified by galectin-10, using immunofluorescence pre-scanning and were subsequently stained red by HE, DFS, and CR. MBP-positive granules surrounding galectin-10-negative cells with degenerated nuclei, indicative of cytolytic degranulation (ETosis), were also stained by HE, DFS, and CR. Non-granular MBP-positive interstitial areas were not visualised by HE, DFS, or CR, suggesting that they did not detect the deposition of granule proteins released from disrupted granules. Eosinophil granules were identified by extracting the red colour using ImageJ software in DFS-stained images, more specifically than in CR-stained or HE-stained images. Cardiologists counted more eosinophils in DFS-stained sections than in HE-stained serial sections within a certain time without miscounting.DFS staining effectively identifies eosinophils and their cell-free granules in cardiac tissues, outperforming HE and CR. DFS may advance the diagnosis and management of eosinophil-related heart diseases.
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