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A single-pool inositol 1,4,5-trisphosphate-receptor-based model for agonist-stimulated oscillations in Ca2+ concentration.

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De Young, G W, Keizer, J·1992·Proceedings of the National Academy of Sciences

Abstract

Relying on quantitative measurements of Ca2+ activation and inhibition of the inositol 1,4,5-trisphosphate (IP3) receptor in the endoplasmic reticulum, we construct a simplified kinetic model to describe the properties of this channel. Selecting rate constants to fit key kinetic and equilibrium data, we find that the model reproduces a variety of in vivo and in vitro experiments. In combination with Ca(2+)-ATPase activity for Ca2+ uptake into the endoplasmic reticulum, the model leads to cytoplasmic oscillations in Ca2+ concentration at fixed IP3 concentration and only a single pool of releasable Ca2+, the endoplasmic reticulum. Incorporation of a positive-feedback mechanism of Ca2+ on IP3 production by phospholipase C enriches the properties of the oscillations and leads to oscillations in Ca2+ concentration accompanied by oscillations in IP3 concentration. We discuss the possible significance of these results for the interpretation of experiments.

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Metadata

Authors
De Young, G. W., & Keizer, J.
Venue
Proceedings of the National Academy of Sciences
Published
1992-10-15
Volume
89
Issue
20
Pages
9895-9899
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2171437709
Cited by
736
References
0
FWCI
6.36
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: A single-pool inositol 1,4,5-trisphosphate-receptor-based model for agonist-stimulated oscillations in Ca2+ concentration. https://app.cochat.ai/papers/10.1073/pnas.89.20.9895
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De Young, G. W., & Keizer, J. (1992). A single-pool inositol 1,4,5-trisphosphate-receptor-based model for agonist-stimulated oscillations in Ca2+ concentration. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.89.20.9895

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.