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Physical attributes of salivary calcium particles and their interaction with gingival epithelium
BACKGROUND: The formation of dental plaque and its involvement in the pathogenesis of periodontitis is a topic of intense interest given the high prevalence of periodontitis in humans. Even though calcium-based particles play an active role in both dental plaque formation and periodontitis, few publ...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chang Gung University
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847823/ https://www.ncbi.nlm.nih.gov/pubmed/35166207 http://dx.doi.org/10.1016/j.bj.2020.05.008 |
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author | Peng, Hsin-Hsin Huang, Pei-Rong Young, John D. Ojcius, David M. |
author_facet | Peng, Hsin-Hsin Huang, Pei-Rong Young, John D. Ojcius, David M. |
author_sort | Peng, Hsin-Hsin |
collection | PubMed |
description | BACKGROUND: The formation of dental plaque and its involvement in the pathogenesis of periodontitis is a topic of intense interest given the high prevalence of periodontitis in humans. Even though calcium-based particles play an active role in both dental plaque formation and periodontitis, few publications describe the physical-chemical properties of these particles. METHODS: Saliva samples were collected from healthy volunteers. From these samples, saliva-derived particles were isolated and stained for calcium using calcein or Fluo-4. The salivary particles were also subjected to characterization by flow cytometry and immunoblotting. Internalization of calcein-labeled salivary particles by gingival epithelial cells was visualized by confocal microscopy. RESULTS: We found that calcium-based salivary particles from healthy volunteers varied greatly in size but were enriched in particles of sizes at or greater than 1.5 μm. Immunoblotting analysis of the salivary particles identified several proteins including albumin, fetuin-A, and statherin, which have been found in calcium phosphate particles from other tissues or are known to modulate calcium homeostasis in saliva. In addition, calcium particles were internalized by both gingival epithelial cells and monocyte-derived macrophages. CONCLUSION: Salivary calcium particles were enriched in the micrometer range, internalized by gingival epithelial cells, and contain albumin, fetuin-A and statherin, regulators of particle formation. These characteristics of the calcium-based salivary particles and their biological activities provide a basis for further studies to understand the molecular basis for pathogenesis of periodontitis. |
format | Online Article Text |
id | pubmed-8847823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Chang Gung University |
record_format | MEDLINE/PubMed |
spelling | pubmed-88478232022-02-25 Physical attributes of salivary calcium particles and their interaction with gingival epithelium Peng, Hsin-Hsin Huang, Pei-Rong Young, John D. Ojcius, David M. Biomed J Original Article BACKGROUND: The formation of dental plaque and its involvement in the pathogenesis of periodontitis is a topic of intense interest given the high prevalence of periodontitis in humans. Even though calcium-based particles play an active role in both dental plaque formation and periodontitis, few publications describe the physical-chemical properties of these particles. METHODS: Saliva samples were collected from healthy volunteers. From these samples, saliva-derived particles were isolated and stained for calcium using calcein or Fluo-4. The salivary particles were also subjected to characterization by flow cytometry and immunoblotting. Internalization of calcein-labeled salivary particles by gingival epithelial cells was visualized by confocal microscopy. RESULTS: We found that calcium-based salivary particles from healthy volunteers varied greatly in size but were enriched in particles of sizes at or greater than 1.5 μm. Immunoblotting analysis of the salivary particles identified several proteins including albumin, fetuin-A, and statherin, which have been found in calcium phosphate particles from other tissues or are known to modulate calcium homeostasis in saliva. In addition, calcium particles were internalized by both gingival epithelial cells and monocyte-derived macrophages. CONCLUSION: Salivary calcium particles were enriched in the micrometer range, internalized by gingival epithelial cells, and contain albumin, fetuin-A and statherin, regulators of particle formation. These characteristics of the calcium-based salivary particles and their biological activities provide a basis for further studies to understand the molecular basis for pathogenesis of periodontitis. Chang Gung University 2021-12 2020-05-23 /pmc/articles/PMC8847823/ /pubmed/35166207 http://dx.doi.org/10.1016/j.bj.2020.05.008 Text en © 2020 Chang Gung University. Publishing services by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Peng, Hsin-Hsin Huang, Pei-Rong Young, John D. Ojcius, David M. Physical attributes of salivary calcium particles and their interaction with gingival epithelium |
title | Physical attributes of salivary calcium particles and their interaction with gingival epithelium |
title_full | Physical attributes of salivary calcium particles and their interaction with gingival epithelium |
title_fullStr | Physical attributes of salivary calcium particles and their interaction with gingival epithelium |
title_full_unstemmed | Physical attributes of salivary calcium particles and their interaction with gingival epithelium |
title_short | Physical attributes of salivary calcium particles and their interaction with gingival epithelium |
title_sort | physical attributes of salivary calcium particles and their interaction with gingival epithelium |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847823/ https://www.ncbi.nlm.nih.gov/pubmed/35166207 http://dx.doi.org/10.1016/j.bj.2020.05.008 |
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