A computational framework for the investigation of phosphoinositide regulation

Hilaire Yam Fung Cheung, Chukiat Tantiwong, Dipali Kale, Jonathan M Gibbins, Steve P Watson, Johan W M Heemskerk, Albert Sickmann, Robert Ahrends and Joanne L Dunster

PLOS Computational Biology, 2025, vol. 21, issue 9, 1-25

Abstract: Phosphoinositides are a group of interconvertible lipids that are located in the membrane of eukaryotic cells. They turnover via complex network of reactions (called the phosphoinositide pathway) that respond rapidly to regulate many aspects of a cell’s response to their environment. Given their low-abundance they are difficult to characterise experimentally. Here we utilise a new experimental method to generate an unusually large dataset that characterises the time-dependent changes in five membrane bound phospoinositides and a soluble inositide in platelet, downstream of its GPVI receptor, where we know the phosphoinositide pathway is particularly active. To shed light on regulatotory steps that are often opaque to experimentation we use this data within a mathematical and computational framework. We construct and assess eleven mathematical models that represent competing interpretations of the dominant mechanisms that regulate the pathway. We find that while four of the models can generate the available data only one model, that incorporates an additional pool of PtdIns, is consistent with the data and is able to successfully predict the effects of an inhibitor. We publish all models openly in a form that is easily usable and adaptable for other researchers to use alongside our or their own data. We studied how changes in the shape and magnitude of events that stimulate the phosphoinositide pathway affect its dynamics. Despite these perturbations, the abundance of Phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) remained stable, consistent with findings reported in the literature.Author summary: Cells use signalling molecules called phosphoinositides to control essential functions like movement, shape, and communication. These molecules are present in very small amounts and change rapidly, making them difficult to study. Here, we focused on platelets, blood cells where phosphoinositide signalling is especially active, using data generated by a new experimental method that describes how six different phosphoinositides change over time after stimulation.

Date: 2025
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Persistent link: https://EconPapers.repec.org/RePEc:plo:pcbi00:1013477

DOI: 10.1371/journal.pcbi.1013477

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