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Record W2790119699 · doi:10.1093/jcag/gwy009.095

A95 INFLAMMATORY PROTEASES DRIVE A MIGRATORY INTESTINAL EPITHELIAL PHENOTYPE THROUGH THE GENERATION OF BIOACTIVE PEPTIDE FRAGMENTS OF E-CADHERIN

2018· article· en· W2790119699 on OpenAlexaffabout
Marilyn Gordon, Anaïs Chauvin, François‐Michel Boisvert, Wallace K. MacNaughton

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2018
Typearticle
Languageen
FieldMedicine
TopicPeptidase Inhibition and Analysis
Canadian institutionsUniversité de SherbrookeUniversity of Calgary
Fundersnot available
KeywordsProteasesWound healingCell biologyNeutrophil elastaseChemistryBiologyBiochemistryMolecular biologyInflammationImmunologyEnzyme

Abstract

fetched live from OpenAlex

The inflammatory microenvironment in the gut contains a variety of proteases which are known to be increased in patient samples in both IBD and CRC. How these proteases and their proteolytic peptide products contribute to wound resolution has been poorly elucidated. A cellular switch from a “barrier” to a “migration/repair” phenotype is required for healing in IBD, but is also a hallmark of tumorigenesis. Proteolytic degradation of epithelial E-cadherin (Ecad) is necessary for this process, we have been studying the biological activity small peptide fragments of Ecad generated by neutrophil elastase, an inflammatory protease elevated in IBD. We have been studying the ability of proteases to induce a switch in the colonic epithelium from a barrier to a repair phenotype (epithelial to mesenchymal transition [EMT]) characterized by increased migration and disrupted homeostasis. To test the hypothesis that inflammatory proteases process Ecad into small bioactive peptides that contribute to wound resolution. Recombinant Ecad was incubated with neutrophil elastase (NE) in vitro to produce NE-dependent Ecad peptides. Six of these peptides shared partial homology with Ecad peptides identified by mass spectrometry in IBD patient samples, and were chosen for further characterization. Peptides were synthesized and assayed for their ability to alter wound healing capacity, proliferation, cell spreading, and cytotoxicity in Caco-2 cells using the IncuCyte™ live-cell imaging system for 48 hours following exposure to 1, 10, and 100 mg/mL concentrations of peptides. All analysis was done using the IncuCyte™ ZOOM platform in conjunction with ImageJ software. We have identified 6 Ecad peptides produced by neutrophil elastase activity that appear to be increased in IBD patient tissue. We have characterized these peptides to have novel biological roles in altering wound resolution and proliferation rates, with 3 peptides showing significantly increased wound healing capacity at at least one concentration. These 3 peptides (KAADTDPTAPPYD, NRNTGVISVV, and LPPEDDTRDNV) showed improved wound closures of approximately 7–10% under serum free conditions and 5–10% under full serum conditions compared to controls. Preliminary data also suggests that these peptides appear to have a positive effect on proliferation rates, and appear to alter cellular morphology of cells to that of a more flattened cell type, typical of repair programming of cells to cover a denuded area. Our data reveal a novel role for proteolytic processing of Ecad under inflammatory conditions, producing bioactive peptides that drive a wound-healing phenotype in epithelial cells in response to damage. CIHRUniversity of Calgary Faculty Seed Grants

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: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.008

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 integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

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 head0.016
GPT teacher head0.247
Teacher spread0.232 · 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".

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Citations0
Published2018
Admission routes2
Has abstractyes

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