Helmholtz Gemeinschaft


An integrate-and-fire approach to Ca(2+) signaling. Part II: Cumulative refractoriness

Item Type:Article
Title:An integrate-and-fire approach to Ca(2+) signaling. Part II: Cumulative refractoriness
Creators Name:Ramlow, L. and Falcke, M. and Lindner, B.
Abstract:Inositol 1,4,5-trisphosphate-induced Ca(2+) signaling is a second messenger system used by almost all eukaryotic cells. The agonist concentration stimulating Ca(2+) signals is encoded in the frequency of a Ca(2+) concentration spike sequence. When a cell is stimulated, the interspike intervals (ISIs) often show a distinct transient during which they gradually increase, a system property we refer to as cumulative refractoriness. We extend a previously published stochastic model to include the Ca(2+) concentration in the intracellular Ca(2+) store as a slow adaptation variable. This model can reproduce both stationary and transient statistics of experimentally observed ISI sequences. We derive approximate expressions for the mean and coefficient of variation of the stationary ISIs. We also consider the response to the onset of a constant stimulus and estimate the length of the transient and the strength of the adaptation of the ISI. We show that the adaptation sets the coefficient of variation in agreement with current ideas derived from experiments. Moreover, we explain why, despite a pronounced transient behavior, ISI correlations can be weak, as often observed in experiments. Finally, we fit our model to reproduce the transient statistics of experimentally observed ISI sequences in stimulated HEK cells. The fitted model is able to qualitatively reproduce the relationship between the stationary interval correlations and the number of transient intervals, as well as the strength of the ISI adaptation. We also find positive correlations in the experimental sequence that cannot be explained by our model.
Keywords:Action Potentials, Neurological Models, Neurons, Signal Transduction
Source:Biophysical Journal
Publisher:Biophysical Society
Page Range:4710-4729
Date:19 December 2023
Official Publication:https://doi.org/10.1016/j.bpj.2023.11.015
PubMed:View item in PubMed

Repository Staff Only: item control page

Open Access
MDC Library