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Record W2921128101 · doi:10.1093/jcag/gwz006.157

A158 ENTEROPATHOGEN CYSTEINE PROTEASES ALTER INTESTINAL MUCUS PRODUCTION VIA PROTEASE-ACTIVATED RECEPTOR-2: EFFECTS OF GIARDIA DUODENALIS

2019· article· en· W2921128101 on OpenAlexaff
Elena Fekete, Christina Amat, Thibault Allain, Morley D. Hollenberg, Kris Chadee, André G. Buret

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2019
Typearticle
Languageen
FieldImmunology and Microbiology
TopicParasitic Infections and Diagnostics
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsProteasesBiologyMucusMicrobiologyMucinGiardiaCysteine proteaseProteaseProtease-activated receptor 2Chinese hamster ovary cellReceptorBiochemistryEnzyme

Abstract

fetched live from OpenAlex

Disruption of the intestinal mucus barrier can impair host innate immunity and has been implicated in many GI disorders. We recently showed that the intestinal protozoan parasite Giardia duodenalis alters host intestinal mucus layers via obscure mechanisms. Giardia offers a powerful model system to study regulatory mechanisms governing intestinal mucus production and secretion in health and disease. As Giardia is known to secrete proteases, we hypothesized that goblet cell mucus production may be regulated via protease-activated receptor-2 (PAR2). To characterize mechanisms responsible for Giardia-mediated alterations of mucus production, including the roles of PAR2 and Giardia proteases. LS174T, a human mucus-producing colon cell line, was infected with Giardia trophozoites (isolates NF, WB, S2, and GSM). Before infection, trophozoites were treated with E64, a broad-spectrum cysteine protease inhibitor, and LS174T were treated with a pepducin PAR2 antagonist, or BAPTA, a calcium chelator. Quantitative PCR (qPCR) was performed for the MUC2 mucin gene. Chinese hamster ovary cells transfected with nano-luciferase tagged PAR2 were incubated with Giardia NF or GSM trophozoites, which cleaved receptors to release enzymes. Luminescence was measured as an indicator of PAR cleavage and therefore potential of Giardia to activate PAR2. Wild-type (WT) and PAR2 deficient (PAR2-/-) mice were infected with Giardia trophozoites. Colonic mucus was stained using fluorescein-coupled wheat-germ agglutinin and qPCR was performed for Muc2 and Muc5ac. Giardia NF, S2, and WB, but not GSM, increased MUC2 gene expression in LS714T. Increases were attenuated by inhibition of Giardia cysteine protease activity and by antagonism of PAR2 or inhibition of calcium release in LS174T. Giardia trophozoites cleaved PAR2 at the N-terminus suggesting they may activate PAR2. Cleavage efficiency was isolate dependent and reflected differences in protease activity between isolates. Cysteine protease inhibition significantly reduced cleavage. Giardia infected WT mice show increased colonic expression of Muc2 and Muc5ac, and increased Muc5ac but decreased Muc2 expression in the jejunum. These changes were not demonstrated in PAR2-/- mice. WT infected and PAR2-/- noninfected mice showed thinning of the colonic mucus layer compared to WT controls. There was some recovery in thickness in PAR2-/- infected mice. Results show that PAR2 plays a significant role in the regulation of mucin gene expression in mice and a human colon cell line. Results suggest that Giardia cysteine proteases cleave and activate PAR2 on intestinal goblet cells, leading to calcium release and ultimately altered mucin gene expression. Findings identify a novel regulatory pathway for goblet cell mucus production in the gut. CCC

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 score0.006

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)0.0020.000

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 head0.004
GPT teacher head0.196
Teacher spread0.192 · 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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Citations1
Published2019
Admission routes1
Has abstractyes

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