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Record W3006879776 · doi:10.1093/jcag/gwz047.043

A44 NOVEL AND HIGHLY SENSITIVE FLOW CYTOMETRIC BASED METHOD FOR CONTINUOUS TRACKING OF INTESTINAL PERMEABILTIY

2020· article· en· W3006879776 on OpenAlexaff
Kuo-Ting Tsai, C Ma, Shauna M. Crowley, John J. Priatel, Bruce A. Vallance

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2020
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGut microbiota and health
Canadian institutionsBurnaby Hospital
Fundersnot available
KeywordsDextranIntestinal permeabilityFlow cytometryOvalbuminPermeability (electromagnetism)Inflammatory Bowel DiseasesChemistryPharmacologyChromatographyImmunologyMolecular biologyBiologyInflammatory bowel diseaseMedicineBiochemistryPathologyMembrane

Abstract

fetched live from OpenAlex

Abstract Background Inflammatory bowel diseases (IBD) are chronic, inflammatory conditions of the intestinal tract. In addition to a complex mixture of genetic, and environmental factors, increased intestinal permeability is also thought to be involved. Despite its diagnostic importance, there is no reliable yet minimally invasive way to measure intestinal permeability in patients and animal models. Currently, most assays involve the detection of orally given sugar molecules in either the urine (MLR method) or the plasma (FITC-dextran). These methods offer only limited accuracy, and do not allow continual tracking of intestinal permeability within the same animal due to the requirement of euthanization. Herein, we describe a novel cytometric-based method using an ingested dietary protein (ovalbumin (OVA)) and flow cytometry. We show our method is reliable, highly sensitive, minimally invasive and allows for the continuous tracking of intestinal permeability within the same individual using small blood volumes. Aims To compare the utility of our bead-based method of intestinal permeability measurement to the FITC-Dextran method. Methods Wildtype (WT) C57BL/6 mice, and mucin 2-deficient (Muc2-/-) mice (known to suffer a leaky gut) at baseline, or mice given chemical or infection-induced colitis were gavaged with a solution containing OVA protein and FITC-Dextran. After 6 hours, mice were euthanized to collect plasma for spectrophotometry (FITC-Dextran), or for flow cytometry (bead-based ELISA) analyses. Results We found that both OVA and FITC-dextran were detectable in plasma samples of the Muc2-/- mice, but not the WT mice, 6 hours after oral co-administration, however the bead-based method produced more consistent readings. Immunostaining of tissue sections with the same antibodies also showed that OVA can readily diffuse through the gut epithelium of Muc2-/- mice but not the WT mice, validating the specificity of the antibodies. We also tested our assay on WT mice undergoing dextran sodium sulfate (DSS) colitis, or infected with Citrobacter rodentium. We found that our method could detect statically significant changes in intestinal permeability 2 to 3 days earlier than the FITC-dextran method, while providing greatly reduced variability between technical repeats. More importantly, we were able to use a small volume (5 μL) of whole blood collected via tail poke, to measure intestinal permeability without requiring euthanization of the mice. This allowed the continuous tracking of permeability changes within the same animal. Conclusions We conclude that the bead-based method is more sensitive and reliable than the FITC-Dextran method as tested in several murine colitis models. More importantly, we showed that the bead-based method allows continual tracking of intestinal permeability within the same animal, enabling time course measurements. Funding Agencies CAG, CCC, CIHR, NRCBC Children’s Research Institute

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)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.002
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0000.001
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0020.002
Insufficient payload (model declined to judge)0.0020.001

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 head0.014
GPT teacher head0.253
Teacher spread0.239 · 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 designBench or experimental
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
Published2020
Admission routes1
Has abstractyes

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