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Kleiber, T.

Publications and source records attributed to Kleiber, T..

2 recordsLinked to original sources

A Bayesian Neural Ordinary Differential Equations Framework to Study the Effects of Chemical Mixtures on Survival

In the field of Plant Protection Products (PPP), the combination of multiple active ingredients is a common strategy to improve the efficacy against target species. However, these mixtures may expose non-target species to untested chemical combinations due to varied application and degradation pathways. Developing a method to predict the effects of such mixtures without extensive testing is crucial for enhancing risk assessment for non-target organisms. Toxicokinetic (TK) and toxicodynamic (TD) models currently provide predictive power for the toxicity of mixture over time, utilizing the concentration addition and independent action principles. However, their capacity to capture complex, non-linear interactions -- such as synergistic and antagonistic effects -- remains limited. To overcome these limitations, we introduce a new methodology that integrates TKTD models using Ordinary Differential Equations (ODE) with neural networks (NN), offering a robust framework for modeling complex substance interactions. The ODE component encodes fundamental biological principles that constrain the neural network to biologically plausible solutions. Bayesian inference further refines the model by addressing uncertainties in data, model parameters, and biological processes, while also allowing quantification of prediction uncertainty, highlighting gaps in experimental data that warrant further investigation. This hybrid model was evaluated across 99 acute toxicity studies that included various PPP mixtures, testing its ability to identify and forecast deviations from expected mixture behaviors. Our findings highlight the potential of combining mechanistic models with machine learning techniques to advance predictive accuracy in environmental toxicology, providing a framework to anticipate the combined effects of untested chemical mixtures and inform risk assessment practices.

pharmacology and toxicology↗

The TFIID subunit Taf4 is required for pancreatic beta cell function and identity.

We selectively inactivated the Taf4 subunit of general transcription factor TFIID in adult murine pancreatic beta cells (BCs). Taf4 inactivation rapidly diminishes expression of critical genes involved in BC function leading to increased glycaemia, lowered plasma insulin levels, defective glucose-stimulated insulin secretion and in the longer term reduced BC mass through apoptosis of a subpopulation of BCs. Nevertheless, glycaemia and blood insulin levels are stabilised after 11 weeks with mutant animals showing long term survival. Bulk RNA-seq and ATAC-seq together with single cell RNA-seq on isolated Langerhans islets show that Taf4 loss leads to a remodelling of chromatin accessibility and gene expression not only in targeted BCs, but also alpha and delta cells. One week after Taf4-loss, cells with mixed BC, alpha and/or delta cell identities were observed as well as a BC population trans-differentiating into alpha-like cells. Computational analysis defines how known critical BC and alpha cell determinants may act in combination with additional transcription factors and the NuRF chromatin remodelling complex to promote BC trans-differentiation.

cell biology↗