Format

Send to

Choose Destination
J Exp Med. 2019 Aug 16. pii: jem.20190679. doi: 10.1084/jem.20190679. [Epub ahead of print]

The Nlrp6 inflammasome is not required for baseline colonic inner mucus layer formation or function.

Author information

1
Department of Medical Biochemistry, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.
2
Wallenberg Laboratory and Sahlgrenska Center for Cardiovascular and Metabolic Research, Department of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
3
Department of Medical Biochemistry, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden george.birchenough@gu.se.

Abstract

The inner mucus layer (IML) is a critical barrier that protects the colonic epithelium from luminal threats and inflammatory bowel disease. Innate immune signaling is thought to regulate IML formation via goblet cell Nlrp6 inflammasome activity that controls secretion of the mucus structural component Muc2. We report that isolated colonic goblet cells express components of several inflammasomes; however, analysis of IML properties in multiple inflammasome-deficient mice, including littermate-controlled Nlrp6-/- , detect a functional IML barrier in all strains. Analysis of mice lacking inflammasome substrate cytokines identifies a defective IML in Il18-/- mice, but this phenotype is ultimately traced to a microbiota-driven, Il18-independent effect. Analysis of phenotypic transfer between IML-deficient and IML-intact mice finds that the Bacteroidales family S24-7 (Muribaculaceae) and genus Adlercrutzia consistently positively covary with IML barrier function. Together, our results demonstrate that baseline IML formation and function is independent of inflammasome activity and highlights the role of the microbiota in determining IML barrier function.

PMID:
31420376
DOI:
10.1084/jem.20190679

Supplemental Content

Full text links

Icon for HighWire
Loading ...
Support Center