Abstract

BackgroundLiver has the unique ability to regenerate following injury, with a wide range of variability of the regenerative response across individuals. Existing computational models of the liver regeneration are largely tuned based on rodent data and hence it is not clear how well these models capture the dynamics of human liver regeneration. Recent availability of human liver volumetry time series data has enabled new opportunities to tune the computational models for human-relevant time scales, and to predict factors that can significantly alter the dynamics of liver regeneration following a resection.MethodsWe utilized a mathematical model that integrates signaling mechanisms and cellular functional state transitions. We tuned the model parameters to match the time scale of human liver regeneration using an elastic net based regularization approach for identifying optimal parameter values. We initially examined the effect of each parameter individually on the response mode (normal, suppressed, failure) and extent of recovery to identify critical parameters. We employed phase plane analysis to compute the threshold of resection. We mapped the distribution of the response modes and threshold of resection in a virtual patient cohort generated in silico via simultaneous variations in two most critical parameters.ResultsAnalysis of the responses to resection with individual parameter variations showed that the response mode and extent of recovery following resection were most sensitive to variations in two perioperative factors, metabolic load and cell death post partial hepatectomy. Phase plane analysis identified two steady states corresponding to recovery and failure, with a threshold of resection separating the two basins of attraction. The size of the basin of attraction for the recovery mode varied as a function of metabolic load and cell death sensitivity, leading to a change in the multiplicity of the system in response to changes in these two parameters.ConclusionsOur results suggest that the response mode and threshold of failure are critically dependent on the metabolic load and cell death sensitivity parameters that are likely to be patient-specific. Interventions that modulate these critical perioperative factors may be helpful to drive the liver regenerative response process towards a complete recovery mode.

Highlights

  • Liver has the unique ability to regenerate following injury, with a wide range of variability of the regenerative response across individuals

  • Activated Kupffer cells release IL-6 which activates JAK-STAT pathway in hepatocytes. This results in the production of immediate early genes (IE) which regulates the priming of hepatocytes

  • We considered a cohort of 1000 virtual patients based on simultaneous variations in both metabolic load and cell death sensitivity parameters, for different levels of resection: 10, 33.3, 66.7, 75 and 90% (Fig. 5a-e), while holding the remaining 31 model parameters fixed at the optimized parameter values

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Summary

Introduction

Liver has the unique ability to regenerate following injury, with a wide range of variability of the regenerative response across individuals. Liver has the ability to fully regenerate post liver injury or surgical resection [1] This process of regeneration takes place via a unique mechanism in which differentiated hepatocytes re-enter the cell cycle to replenish lost cells [2]. This is followed by proliferation of non-parenchymal cells to eventually reconstitute the cell types in the liver tissue, and tissue remodeling to re-establish the lobular scale morphology [3]. This unique regenerative capacity enables majority of clinical interventions into liver disease via surgical resection, as well as live donor transplants and smallfor-size liver transplants. These studies demonstrate that a unified set of cellular and molecular mechanisms, with associated parameters, can account for differences in the regenerative response to varying levels of resection [15], with failure above a threshold [16]

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