4.5 Article

Asymmetric distribution of TLR3 leads to a polarized immune response in human intestinal epithelial cells

Journal

NATURE MICROBIOLOGY
Volume 5, Issue 1, Pages 181-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41564-019-0594-3

Keywords

-

Categories

Funding

  1. Chica and Heinz Schaller Foundation
  2. Deutsche Forschungsgemeinschaft [240245660, SFB 1129, 278001972, TRR186]
  3. European Union's Seventh Framework Programme [334336]
  4. Olympia Morata Fellowship from the Heidelberg University Hospital
  5. Brigitte-Schlieben Lange Program from the state of Baden Wurttemberg, Germany
  6. CellNetworks
  7. NIH [5R01AI093589]

Ask authors/readers for more resources

Intestinal epithelial cells (IECs) act as a physical barrier separating the commensal-containing intestinal tract from the sterile interior. These cells have found a complex balance allowing them to be prepared for pathogen attacks while still tolerating the presence of bacterial or viral stimuli present in the lumen of the gut. Using primary human IECs, we probed the mechanisms that allow for such a tolerance. We discovered that viral infections emanating from the basolateral side of IECs elicit a stronger intrinsic immune response in comparison to lumenal apical infections. We determined that this asymmetric immune response is driven by the clathrin-sorting adaptor AP-1B, which mediates the polarized sorting of Toll-like receptor 3 (TLR3) towards the basolateral side of IECs. Mice and human IECs lacking AP-1B showed an exacerbated immune response following apical stimulation. Together, these results suggest a model where the cellular polarity program plays an integral role in the ability of IECs to partially tolerate apical commensals while remaining fully responsive to invasive basolateral pathogens.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available