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Comparative electron microscopic visualization of the lung alveolar epithelial glycocalyx with different staining and
Vladimir Gluhovic1, Sara Timm1,2, Wolfgang M Kuebler3,4,5,6,7
1Institute of Functional Anatomy, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Insights
This study evaluated cytochemical staining methods for visualizing the lung's alveolar epithelial glycocalyx. Alcian blue and specific lectins effectively labeled glycans, aiding ultrastructural analysis in animal models.
Area of Science:
- Pulmonary biology
- Cell biology
- Microscopy
Background:
- The lung's alveolar surface features a lining layer containing surfactant and the alveolar epithelial glycocalyx.
- Understanding the alveolar epithelial glycocalyx requires effective ultrastructural visualization techniques.
Purpose of the Study:
- To systematically re-evaluate routine cytochemical methods for visualizing the alveolar epithelial glycocalyx.
- To assess specific glycan components, including sialic acid and fucose, within the glycocalyx.
Main Methods:
- Chemical fixation of mouse lungs via vascular perfusion with aldehydes.
- Comparison of cytochemical stains: alcian blue, ruthenium red, and lanthanum nitrate.
- Specific lectin labeling using Sambucus nigra lectin (SNL) for sialic acid and Ulex europaeus agglutinin I (UEA1) for fucose.
Main Results:
- Alcian blue provided the strongest staining, revealing cloud-like structures.
- Ruthenium red showed thread-like structures; lanthanum nitrate did not stain the glycocalyx.
- Both SNL and UEA1 demonstrated specific labeling for sialic acid and fucose, respectively.
Conclusions:
- Established cytochemical staining methods, particularly alcian blue and lectin labeling, are suitable for routine ultrastructural assessment of the alveolar epithelial glycocalyx.
- These techniques can be applied to experimental in vivo models to study glycocalyx changes under various physiological and pathological conditions.
- Tissue massage and post-embedding lectin labeling support animal welfare principles (3Rs).
Abstract:
The alveolar surface of the lung is lined by an epithelium consisting of type I (AECI) and type II alveolar epithelial cells (AECII). This epithelium is covered by a liquid alveolar lining layer (ALL). Besides intra-alveolar surfactant, ALL also contains the alveolar epithelial glycocalyx on the apical side of AECI and AECII. To better understand the alveolar epithelial glycocalyx, its ultrastructural visualization by transmission electron microscopy is required. The aim of this study was to systematically re-evaluate routine cytochemical methods for visualization of the alveolar epithelial glycocalyx and specifically its glycan components. For this purpose, we used chemical fixation by vascular perfusion with aldehydes as a common routine approach in mice. After fixation, staining is needed for glycocalyx visualization. Cytochemical staining agents such as alcian blue, ruthenium red, and lanthanum nitrate were compared. In addition, SNL (Sambucus nigra lectin) and UEA1 (Ulex europaeus agglutinin I) were used for sialic acid and fucose-specific labeling. Alcian blue showed the strongest staining, with cloud-like structures, whereas ruthenium red appeared as thread-like structures. On the other hand, lanthanum nitrate did not stain the alveolar epithelial glycocalyx. For specific sialic acid and fucose labeling, both lectins presented a specific signal. In conclusion, these methods can be used routinely for assessing ultrastructural changes of the alveolar epithelial glycocalyx in experimental in vivo models under different physiological and pathological conditions. In addition, cytochemical staining by tissue massage and post-embedding lectin labeling after vascular perfusion support 3R (reduction, refinement, replacement) principles of animal welfare.
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