Dynamics of Computational Islet Simulations: Islets with Majority Mutated Open K_ATP Channels Retain Bursting
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Gearhart, Gemma, Shuai Jiang, Thomas J. May, et al. “Dynamics of Computational Islet Simulations: Islets with Majority Mutated Open K_ATP Channels Retain Bursting.” Letters in Biomathematics 1, no. 1 (2014): 1. https://doi.org/10.30707/LiB1.1Gearhart.
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This work was written as part of one of the author's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
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Abstract
The study of pancreatic beta-cells comprises a crucial part of the study of the group of diseases known as diabetes. These cells exist in groups known as islets of Langerhans and are responsible for storing and producing insulin. They exhibit electrical bursting behavior during insulin production that correlates with the rate at which insulin is secreted into the bloodstream. Coupling is a natural process within islets that enables the cells to communicate with one another and transfer various ions and electrical currents; coupling of both voltage and metabolites can occur. We model multicellular islets using an existing system of seven ordinary differential equations to model beta cell function. We simulate cells with mutated KATP channels that remain open indefinitely, which have been described in experimental studies but not yet modeled. Simulations run with these mutations reveal the existence of a bursting death threshold, described by the least percentage of cells in the islet that must be mutated for electrical bursts to completely disappear. We determine that this threshold is independent of coupling strengths, cell distribution, and possibly islet dimension; however, we also determined that this threshold is dependent on the glucose influx rate.