A Novel Non-invasive Method to Detect RELM Beta Transcript in Gut Barrier Related Changes During a Gastrointestinal Nematode Infection.
Animals
Biomarkers
/ analysis
Cytokines
/ analysis
Epithelial Cells
/ physiology
Female
Gastrointestinal Diseases
/ parasitology
Intercellular Signaling Peptides and Proteins
/ metabolism
Intestinal Mucosa
/ parasitology
Mice
Mice, Inbred BALB C
Nematospiroides dubius
/ immunology
Strongylida Infections
/ immunology
Tight Junctions
/ physiology
RELM-β
feces
gut barrier
intestinal nematode
non-invasive method
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2019
2019
Historique:
received:
14
12
2018
accepted:
19
02
2019
entrez:
28
3
2019
pubmed:
28
3
2019
medline:
8
9
2020
Statut:
epublish
Résumé
Currently, methods for monitoring changes of gut barrier integrity and the associated immune response via non-invasive means are limited. Therefore, we aimed to develop a novel non-invasive technique to investigate immunological host responses representing gut barrier changes in response to infection. We identified the mucous layer on feces from mice to be mainly composed of exfoliated intestinal epithelial cells. Expression of RELM-β, a gene prominently expressed in intestinal nematode infections, was used as an indicator of intestinal cellular barrier changes to infection. RELM-β was detected as early as 6 days post-infection (dpi) in exfoliated epithelial cells. Interestingly, RELM-β expression also mirrored the quality of the immune response, with higher amounts being detectable in a secondary infection and in high dose nematode infection in laboratory mice. This technique was also applicable to captured worm-infected wild house mice. We have therefore developed a novel non-invasive method reflecting gut barrier changes associated with alterations in cellular responses to a gastrointestinal nematode infection.
Identifiants
pubmed: 30915083
doi: 10.3389/fimmu.2019.00445
pmc: PMC6423163
doi:
Substances chimiques
Biomarkers
0
Cytokines
0
Intercellular Signaling Peptides and Proteins
0
Retnlb protein, mouse
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
445Références
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