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Record W4407285299 · doi:10.1093/jcag/gwae059.014

A14 INVESTIGATING THE IMPACT OF PARKINSON’S DISEASE-ASSOCIATED GENE <i>PINK1</i> ON INTESTINAL HOMEOSTASIS AND RESPONSE TO INFECTION

2025· article· en· W4407285299 on OpenAlexaff
Jessica Pei, Sherilyn Junelle Recinto, Alexandra Kazanova, Lindsay Burns, Adam MacDonald, C Gavino, Michel Desjardins, Jo Anne Stratton, Samantha Gruenheid

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2025
Typearticle
Languageen
FieldMedicine
TopicChild Nutrition and Feeding Issues
Canadian institutionsUniversité de MontréalMcGill University
Fundersnot available
KeywordsPINK1Parkinson's diseaseHomeostasisDiseaseGeneNeuroscienceBiologyMedicineGeneticsParkinCell biologyInternal medicine

Abstract

fetched live from OpenAlex

Abstract Background Intestinal epithelial cells (IECs) provide an essential physical barrier between luminal contents and host tissue. Dysregulation of IECs leads to barrier dysfunction, causing pathologies in both intestinal and extra-intestinal diseases. While Parkinson’s Disease (PD) is primarily a neurodegenerative disorder, increasing evidence links PD progression and gastrointestinal dysfunction. Our group developed a model to investigate the role of the gut in PD, demonstrating that mice with genetic ablation of the PD-associated gene Pink1 exhibited motor phenotypes only when previously infected with gram-negative Citrobacter rodentium intestinal bacteria. As Pink1 is expressed in IECs and the colonic lamina propria, we hypothesize that PD-associated gene mutations directly affect the epithelium and impact early PD pathophysiology. Aims 1. To characterize the transcriptional profiles of Pink1 WT and KO IECs at baseline and following in vivo C. rodentium infection. 2. Use in vitro cell line and colonic organoid systems to study the effect of Pink1 on epithelial activity in an isolated system. Methods Single-cell RNA sequencing was performed on colonic IECs isolated from Pink1 WT and KO mice, at steady state and following in vivo C. rodentium infection. Mice were sacrificed at D6 post infection to elucidate transcriptional differences between IEC lineages of each genotype. To validate scRNAseq findings, we derived ex vivo colonoids from Pink1 WT and KO mouse crypts and used a Pink1 KO CMT-93 epithelial cell line with WT clone as control. The cultures were treated with lipopolysaccharide (LPS), or infected with gram-negative pathogens to determine how PINK1 loss-of-function affects the inflammatory response of the epithelium. Results At baseline, our data revealed upregulation of interferon (IFN)-signaling genes (ISGs) in Pink1 KO enterocytes (ECs) compared to WT; whereby more than 70% of upregulated differentially expressed genes were linked to type I or II IFN signaling. In vitro stimulation of Pink1 KO epithelial cell line with IFN resulted in stark upregulation of ISGs compared to WT. During infection, Pink1 KO ECs demonstrated significant alterations in actin-cytoskeleton-related GO term pathways compared to WT. Infection of Pink1 KO CMT-93 epithelial cells revealed morphological changes in F-actin structures. Conclusions Using in vivo and in vitro models encompassing PD-genetic susceptibility and environmental stimuli, we identified dysregulation in Pink1 KO epithelium, suggesting altered inflammatory responses at baseline and infection. By investigating PD-associated genes in IECs, we will contribute to better understanding the role of the intestine in PD initiation, progression, and pathogenesis. Funding Agencies CAG, CIHR

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.009

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0030.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.013
GPT teacher head0.272
Teacher spread0.260 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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