Previous studies on the development of the parotid gland in various mammals have demonstrated that terminal clusters and acini contain mucous cells during the early postnatal period. However, little information has been available concerning the exact fate of the secretory granules in the mucous cells, specifically as to whether or not the mucous cells differentiate into serous cells. The present study aimed to determine the time of appearance of the mucous cells in the rat parotid gland as well as the morphological and histochemical changes of their granules. Light microscopy showed that cells positively stained with periodic-acid Schiff and alcian blue were sparsely distributed in the terminal clusters and acini on day 1 but had multiplied to a maximal level by day 5. They decreased in number on day 8 and were not recognizable at all by day 10. Electron microscopy revealed that the mucous cells initially contained granules of homogeneous low electron density, and then bipartite and tripartite granules with electron-dense cores were detected. By day 8 granules showing bipartite and tripartite structures and granules of homogeneous high electron density were seen to coexist in single cells. These observations suggest that mucous cells exist in parotid glands for a limited period of time and that, as the gland develops, the mucous granules come to resemble serous granules. Lectin histochemistry indicated that the secretory granules in the mucous cells were positive for peanut agglutinin, soybean agglutinin and wheat germ agglutinin, suggesting the occurrence of beta -D-galactose, alpha -D-N-acetyl galactosamine and beta -D-N-acetyl glucosamine which are the same sugar residues as those found in the granules of mature parotid serous cells. Immunostaining showed that even the low electron-dense granules in the mucous cells were weakly reactive for anti-rat parotid gland amylase; this reactivity gradually increased with development. These results suggest that mucous cell secretory granules which contain abundant glycoconjugate for a limited period during the development of the gland may change into serous granules.
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http://dx.doi.org/10.1679/aohc.60.185 | DOI Listing |
Front Allergy
January 2025
Research Institute of Biomedical Sciences, University Center of Health Sciences, University of Guadalajara, Guadalajara, Mexico.
Allergies are closely associated with sex-related hormonal variations that influence immune function, leading to distinct symptom profiles. Similar sex-based differences are observed in other immune disorders, such as autoimmune diseases. In allergies, women exhibit a higher prevalence of atopic conditions, such as allergic asthma and eczema, in comparison to men.
View Article and Find Full Text PDFOxf Med Case Reports
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Department of Pathology, Okayama Saiseikai General Hospital, 1-17-18 Ifuku-Cho, Kita-Ku, Okayama-shi, Okayama 700-8551, Japan.
Autoimmune gastritis (AIG) is a chronic condition in which the body's immune system mistakenly attacks the stomach lining, specifically targeting parietal cells that produce stomach acid and intrinsic factors. After the infection was eradicated, AIG developed in an elderly woman with symptoms of the disease. 1.
View Article and Find Full Text PDFJ Cell Sci
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Institute of Anatomy and Experimental Morphology, Center for Experimental Medicine, University Cancer Center Hamburg, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Desmosomes are adhesive cell contacts abundant in tissues exposed to mechanical strain, such as the stratified and simple epithelia of the epidermis and mucous membranes, as well as the myocardium. Besides their role in mechanical cell cohesion, desmosomes also modulate pathways important for tissue differentiation, wound healing and immune responses. Dysfunctional desmosomes, resulting from pathogenic variants in genes encoding desmosomal components, autoantibodies targeting desmosomal adhesion molecules or inflammation, cause the life-threatening diseases arrhythmogenic cardiomyopathy and pemphigus and contribute to the pathogenesis of inflammatory bowel diseases.
View Article and Find Full Text PDFInt Med Case Rep J
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Department of Pediatric Ophthalmology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Introduction: Rhabdomyosarcoma (RMS) originates from undifferentiated mesenchymal cells that give rise to striated muscles. The symptoms of para-meningeal RMS often resemble those of allergic rhinosinusitis, including nasal congestion, mucus discharge, headache, and occasional nosebleeds. We report a child with atypical clinical presentation of ocular hypertropia secondary to para-meningeal RMS.
View Article and Find Full Text PDFThe Aim Of The Study: To study the expression of NOD receptors of immunotropic periodontal tissue cells in patients with aggressive periodontitis before and after complex treatment.
Materials And Methods: 15 patients aged 22 to 36 years with aggressive periodontitis were examined before and 21 days after the start of complex treatment. 15 patients with fibroids of the oral mucosa without signs of inflammation served as controls.
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