Ultrastructure of the nonciliated bronchiolar epithelial (Clara) cell of mammalian lung: II. A comparison of horse, steer, sheep, dog, and cat.
Abstract: Two morphologic characteristics have been used to define the nonciliated bronchiolar epithelial cell: abundant agranular endoplasmic reticulum (AER) and membrane-bound avoid granules. To assess the ultrastructural homogeneity of this cell type in the lungs of large domestic mammals used as experimental models in pulmonary research, we evaluated lungs of horse, steer, sheep, dog, and cat. Bronchioles of known anatomic location were examined by electron microscopy following fixation by airway infusion at standard pressure and processing by selective embedding techniques. Nonciliated bronchiolar epithelium of the horse and sheep had numerous avoid granules (averaging above 15 per cell) and abundant AER. Granules were scarce (averaging less than 2 per cell) in steer and dog and absent in cat. AER was minimal in these species compared to horse and sheep. Glycogen was the dominant cytoplasmic feature in steer, dog, and cat, variable in sheep and rare in horse. Large mitochondria with few cristae and densely staining matrix were present only in cat. We concluded that nonciliated bronchiolar cells of horse and sheep were similar in essential features to this cell type in laboratory mammals, having granules and AER in abundance, while those of steer, dog, and cat were not.
Publication Date: 1980-06-01 PubMed ID: 7194780DOI: 10.3109/01902148009069645Google Scholar: Lookup
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- Comparative Study
- Journal Article
Summary
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The researchers compared certain features in the lung cells of five different mammals: horses, steers, sheep, dogs, and cats. They found common structures in the horse and sheep, while the steer, dog, and cat differed significantly.
Methodology
- The subject of the research were the nonciliated bronchiolar epithelial cells, specifically looking at the agranular endoplasmic reticulum (AER) – a cell component involved in protein synthesis and lipid metabolism – and membrane-bound avoid granules.
- The researchers selected five animals commonly used in pulmonary research – horse, steer, sheep, dog, and cat. They looked at the lungs of these animals and prepared them using standard fixation via airway infusion and selective embedding techniques for examination under electron microscopy.
Results
- The nonciliated bronchiolar epithelium of the horse and sheep had numerous avoid granules (averaging more than 15 per cell) and abundant agranular endoplasmic reticulum (AER).
- In contrast, granules were scarce in steers and dogs (averaging less than 2 per cell) and entirely absent in cats. AER was much less abundant in these three species compared to horses and sheep.
- Another notable finding was that the main feature within the cytoplasm – a jelly-like substance that fills a cell – differed across species. Glycogen, a form of energy storage in animals, dominated the cytoplasm of the steer, dog, and cat cells. It was variable in sheep and rare in horses.
- Only cat cells exhibited large mitochondria – the “powerhouse” of a cell – with few cristae (internal compartments) and densely staining matrix, a substance within the mitochondria.
Conclusion
- The researchers concluded that the nonciliated bronchiolar cells of horses and sheep had similar structural features to the same cell types found in common laboratory mammals – abundant granules and AER.
- Meanwhile, in steers, dogs, and cats, these cells were structurally different, having far fewer granules and minimal AER. This could implicate differences in the lung cell function across species.
This study implies the careful selection and use of animal models in pulmonary research, as differences in the cellular structure may affect the applicability of findings across different species.
Cite This Article
APA
Plopper CG, Mariassy AT, Hill LH.
(1980).
Ultrastructure of the nonciliated bronchiolar epithelial (Clara) cell of mammalian lung: II. A comparison of horse, steer, sheep, dog, and cat.
Exp Lung Res, 1(2), 155-169.
https://doi.org/10.3109/01902148009069645 Publication
Researcher Affiliations
MeSH Terms
- Animals
- Cats
- Cattle
- Cytoplasmic Granules
- Dogs
- Endoplasmic Reticulum
- Epithelial Cells
- Epithelium / ultrastructure
- Female
- Glycogen
- Golgi Apparatus
- Horses
- Lung / ultrastructure
- Male
- Mitochondria
- Sheep
Citations
This article has been cited 9 times.- Blackburn JB, Li NF, Bartlett NW, Richmond BW. An update in club cell biology and its potential relevance to chronic obstructive pulmonary disease.. Am J Physiol Lung Cell Mol Physiol 2023 May 1;324(5):L652-L665.
- Côté O, Lillie BN, Hayes MA, Clark ME, van den Bosch L, Katavolos P, Viel L, Bienzle D. Multiple secretoglobin 1A1 genes are differentially expressed in horses.. BMC Genomics 2012 Dec 19;13:712.
- Smith RW, Hicks DA, Reynolds SD. Roles for β-catenin and doxycycline in the regulation of respiratory epithelial cell frequency and function.. Am J Respir Cell Mol Biol 2012 Jan;46(1):115-24.
- Vanspauwen MJ, Linssen CF, Bruggeman CA, Jacobs JA, Drent M, Bergmans DC, van Mook WN. Clara cell protein in bronchoalveolar lavage fluid: a predictor of ventilator-associated pneumonia?. Crit Care 2011;15(1):R14.
- van Riel D, Rimmelzwaan GF, van Amerongen G, Osterhaus AD, Kuiken T. Highly pathogenic avian influenza virus H7N7 isolated from a fatal human case causes respiratory disease in cats but does not spread systemically.. Am J Pathol 2010 Nov;177(5):2185-90.
- Xing Y, Li C, Li A, Sridurongrit S, Tiozzo C, Bellusci S, Borok Z, Kaartinen V, Minoo P. Signaling via Alk5 controls the ontogeny of lung Clara cells.. Development 2010 Mar;137(5):825-33.
- Armit CJ, O'Dea S, Clarke AR, Harrison DJ. Absence of p53 in Clara cells favours multinucleation and loss of cell cycle arrest.. BMC Cell Biol 2002 Nov 21;3:27.
- Giangreco A, Reynolds SD, Stripp BR. Terminal bronchioles harbor a unique airway stem cell population that localizes to the bronchoalveolar duct junction.. Am J Pathol 2002 Jul;161(1):173-82.
- Palmer KC. Clara cell adenomas of the mouse lung. Interaction with alveolar type 2 cells.. Am J Pathol 1985 Sep;120(3):455-63.
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