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A mathematical model of calcium dynamics in HSY cells

Saliva is an essential part of activities such as speaking, masticating and swallowing. Enzymes in salivary fluid protect teeth and gums from infectious diseases, and also initiate the digestion process. Intracellular calcium (Ca(2+)) plays a critical role in saliva secretion and regulation. Experim...

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Detalles Bibliográficos
Autores principales: Han, Jung Min, Tanimura, Akihiko, Kirk, Vivien, Sneyd, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310762/
https://www.ncbi.nlm.nih.gov/pubmed/28199326
http://dx.doi.org/10.1371/journal.pcbi.1005275
Descripción
Sumario:Saliva is an essential part of activities such as speaking, masticating and swallowing. Enzymes in salivary fluid protect teeth and gums from infectious diseases, and also initiate the digestion process. Intracellular calcium (Ca(2+)) plays a critical role in saliva secretion and regulation. Experimental measurements of Ca(2+) and inositol trisphosphate (IP(3)) concentrations in HSY cells, a human salivary duct cell line, show that when the cells are stimulated with adenosine triphosphate (ATP) or carbachol (CCh), they exhibit coupled oscillations with Ca(2+) spike peaks preceding IP(3) spike peaks. Based on these data, we construct a mathematical model of coupled Ca(2+) and IP(3) oscillations in HSY cells and perform model simulations of three different experimental settings to forecast Ca(2+) responses. The model predicts that when Ca(2+) influx from the extracellular space is removed, oscillations gradually slow down until they stop. The model simulation of applying a pulse of IP(3) predicts that photolysis of caged IP(3) causes a transient increase in the frequency of the Ca(2+) oscillations. Lastly, when Ca(2+)-dependent activation of PLC is inhibited, we see an increase in the oscillation frequency and a decrease in the amplitude. These model predictions are confirmed by experimental data. We conclude that, although concentrations of Ca(2+) and IP(3) oscillate, Ca(2+) oscillations in HSY cells are the result of modulation of the IP(3) receptor by intracellular Ca(2+), and that the period is modulated by the accompanying IP(3) oscillations.