AI Article Synopsis

  • γδ TCR-expressing intraepithelial lymphocytes (γδ IELs) are crucial for monitoring the intestinal epithelium, but how they move within this area hasn't been thoroughly studied.
  • Research shows that IL-15 significantly influences the migration and positioning of γδ IELs, with overexpression in the lamina propria leading to their mislocation away from the epithelium.
  • The study highlights that IL-15 helps maintain γδ IEL mobility and that disruptions in its signaling can lead to increased vulnerability to pathogen invasion, underscoring its importance in intestinal immune defense.

Article Abstract

Intraepithelial lymphocytes (IELs) expressing the γδ TCR (γδ IELs) provide continuous surveillance of the intestinal epithelium. However, the mechanisms regulating the basal motility of these cells within the epithelial compartment have not been well defined. We investigated whether IL-15 contributes to γδ IEL localization and migratory behavior in addition to its role in IEL differentiation and survival. Using advanced live cell imaging techniques in mice, we find that compartmentalized overexpression of IL-15 in the lamina propria shifts the distribution of γδ T cells from the epithelial compartment to the lamina propria. This mislocalization could be rescued by epithelial IL-15 overexpression, indicating that epithelial IL-15 is essential for γδ IEL migration into the epithelium. Furthermore, in vitro analyses demonstrated that exogenous IL-15 stimulates γδ IEL migration into cultured epithelial monolayers, and inhibition of IL-2Rβ significantly attenuates the basal motility of these cells. Intravital microscopy showed that impaired IL-2Rβ signaling induced γδ IEL idling within the lateral intercellular space, which resulted in increased early pathogen invasion. Similarly, the redistribution of γδ T cells to the lamina propria due to local IL-15 overproduction also enhanced bacterial translocation. These findings thus reveal a novel role for IL-15 in mediating γδ T cell localization within the intestinal mucosa and regulating γδ IEL motility and patrolling behavior as a critical component of host defense.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6075741PMC
http://dx.doi.org/10.4049/jimmunol.1701603DOI Listing

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