Skip to main navigation Skip to search Skip to main content

Mapping Signaling Mechanisms in Neurotoxic Injury from Sparsely Sampled Data Using a Constraint Satisfaction Framework

  • Jeffery Page
  • , Kimberly A. Kelly
  • , Lindsay T. Michalovicz
  • , James P. O’Callahghan
  • , Shichen Shen
  • , Xiaoyu Zhu
  • , Jun Qu
  • , Jonathan Boyd
  • , Gordon Broderick
  • Rochester General Hospital
  • National Institute for Occupational Safety and Health
  • SUNY Buffalo
  • Virginia Commonwealth University

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

Abstract

Gulf War Illness (GWI) is a poorly understood exposure-induced neuroinflammatory disorder where complexity and the high cost of animal exposure studies has led to fragmented and sparse data sets incompatible with conventional data mining. We propose a numerical approach for generating hypotheses from sparse data to describe dysregulation of phosphoproteomic signaling in GWI brain. In an established animal model, hippocampus, and prefrontal cortex (PFC) samples were collected in mice exposed to corticosterone (CORT) to mimic high physiological stress, sarin surrogate diisopropyl fluorophosphate (DFP), CORT and DFP (CORT+DFP), as well as controls. IonStar liquid chromatography/ mass spectrometry (LC/MS) profiling produced a network of 93 undirected interactions (Pearson correlation Bonferroni<1%) linking 12 hippocampal and 5 PFC phosphoproteins. With only one pre-treatment resting state and one post-treatment transient observation, conventional rate models were infeasible. Instead, a simple discrete state transition logic was applied to each network node requiring baseline be a steady state from which the network could evolve through the transient 6-h post-treatment state. Solving this as a Constraint Satisfaction (SAT) problem produced 3 competing network models where DFP directly targeted phosphorylated subspecies of sodium channel protein type 1 subunit alpha (Scn1a), protein kinase C gamma (Prkcg), sacsin molecular chaperone (Sacs), in PFC and R3H domain containing 2 (R3hdm2) in hippocampus potentiated by corticosteroids. In simulation-based searches for intervention targets inhibition of Prkcg was disproportionately represented in rescuing the model-predicted persistent illness state, though companion targets were also necessary. Results such as these suggest that a dynamically constrained model-informed design can be highly useful in the initial phases of investigation into complex poorly understood illness where detailed data is largely unavailable.

Original languageEnglish
Title of host publicationAugmented Cognition - 18th International Conference, AC 2024, Held as Part of the 26th HCI International Conference, HCII 2024, Proceedings
EditorsDylan D. Schmorrow, Cali M. Fidopiastis
PublisherSpringer Science and Business Media Deutschland GmbH
Pages95-110
Number of pages16
ISBN (Print)9783031615689
DOIs
StatePublished - 2024
Event18th International Conference on Augmented Cognition, AC 2024, held as part of the 26th HCI International Conference, HCII 2024 - Washington, United States
Duration: Jun 29 2024Jul 4 2024

Publication series

NameLecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
Volume14694 LNAI
ISSN (Print)0302-9743
ISSN (Electronic)1611-3349

Conference

Conference18th International Conference on Augmented Cognition, AC 2024, held as part of the 26th HCI International Conference, HCII 2024
Country/TerritoryUnited States
CityWashington
Period06/29/2407/4/24

Keywords

  • animal model
  • network regulatory dynamics
  • Neurotoxic insult

Fingerprint

Dive into the research topics of 'Mapping Signaling Mechanisms in Neurotoxic Injury from Sparsely Sampled Data Using a Constraint Satisfaction Framework'. Together they form a unique fingerprint.

Cite this