Evidence map›Paper›PMID 41103154›Full record

ArticleEnvironmental science & technology2025

Acrolein-Induced Alterations in Morphology and Stress Resilience in hiPSC-Derived Cortical Neurons.

Junkai Xie, Shichen Wu, Xihui Zhao, Anke M Tukker, Han Zhao, Sehong Min, Oscar F Sanchez, Jean-Christophe Rochet, Aaron B Bowman, Riyi Shi and 1 more

Abstract read
In one paragraph

Article in Environmental science & technology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Junkai XieDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Shichen WuDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Xihui ZhaoWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Anke M TukkerSchool of Health Sciences, Purdue University, West Lafayette, Indiana 47907, United States.ORCID 0000-0001-8973-4809
Han ZhaoDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Sehong MinBorch Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana 47907, United States.
Oscar F SanchezDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Jean-Christophe RochetBorch Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana 47907, United States.ORCID 0000-0002-6484-1541
Aaron B BowmanSchool of Health Sciences, Purdue University, West Lafayette, Indiana 47907, United States.
Riyi ShiWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Chongli YuanDavidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.ORCID 0000-0003-3765-0931

Funding

Modeling functional genomics of susceptibility to the persistent effects of environmental toxins in an elderly rural Indiana neurodegenerative cohortR01AG080917 · NIA · PURDUE UNIVERSITY · PI Aaron B Bowman, Chongli Yuan · 2022 to 2026
$4.1M
NIA NIH HHS R01 AG080917
6 · The paper itself

Abstract

Acrolein, an α,β-unsaturated aldehyde and reactive oxygen species (ROS), originates from both endogenous mechanisms, such as lipid peroxidation, and exogenous sources, including the decomposition of organic matter. Elevated levels of acrolein are detected in the brains of individuals with Alzheimer's and Parkinson's diseases, as well as those with traumatic brain or spinal cord injuries. Environmental exposure, including smoking and industrial emissions, further contribute to acrolein accumulation. Despite their recognized immediate neurotoxic effects, the chronic implications on neurodegeneration remain elusive. To elucidate these effects, human induced pluripotent stem cell (hiPSC)-derived human cortical neurons (∼Day 60 postdifferentiation) were subjected to 0, 1, and 10 μM concentrations of acrolein for 2 days following a nonexposure relaxation period (7 days) to assess the persistence of the resulting phenotypes. Immunofluorescence and calcium imaging demonstrated sustained alterations in the synaptic density and neuronal activity in acrolein-exposed differentiated neurons. Moreover, a persistent and dose-dependent neuronal hyperactivity was identified through microelectrode array analysis. Acrolein exposure also precipitated sustained elevations in Alzheimer's Disease-related phosphorylated Tau (p-tau) pathology and mitochondrial stress, along with diminished cellular resilience to subsequent stressors. Collectively, these findings support a persistent neurotoxic effect of acrolein, highlighting its potential implications for neurodegenerative disorders.

Indexed as

AcroleinReactive Oxygen SpeciesAlzheimer DiseaseCerebral CortexEnvironmental ExposureHumansInduced Pluripotent Stem CellsNeuronsParkinson DiseaseAcroleinReactive Oxygen Speciesacrolein exposureneurodegenerationreactive oxygen speciesspontaneous neuronal activitytau

Identifiers

PMID41103154
PMCPMC13036998

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.