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Inflammasome-independent functions of NAIPs and NLRs in the intestinal epithelium
- Source :
- Biochemical Society Transactions
- Publication Year :
- 2021
- Publisher :
- Portland Press Ltd., 2021.
-
Abstract
- The gut relies on the complex interaction between epithelial, stromal and immune cells to maintain gut health in the face of food particles and pathogens. Innate sensing by the intestinal epithelium is critical for maintaining epithelial barrier function and also orchestrating mucosal immune responses. Numerous innate pattern recognition receptors (PRRs) are involved in such sensing. In recent years, several Nucleotide-binding-domain and Leucine-rich repeat-containing receptors (NLRs) have been found to partake in pathogen or damage sensing while also being implicated in gut pathologies, such as colitis and colorectal cancer (CRC). Here, we discuss the current literature focusing on NLR family apoptosis inhibitory proteins (NAIPs) and other NLRs that have non-inflammasome roles in the gut. The mechanisms behind NLR-mediated protection often converges on similar signalling pathways, such as STAT3, MAPK and NFκB. Further understanding of how these NLRs contribute to the maintenance of gut homeostasis will be important for understanding gut pathologies and developing new therapies.
- Subjects :
- MAPK/ERK pathway
Immunology & Inflammation
Stromal cell
Inflammasomes
NLR Proteins
Biology
Biochemistry
Immune system
inflammasome
Host-Microbe Interactions
medicine
Animals
Humans
Intestinal Mucosa
Receptor
Review Articles
innate immunity
Cancer
Innate immune system
Pattern recognition receptor
nod-like receptors
Inflammasome
Gastrointestinal, Renal & Hepatic Systems
Intestinal epithelium
Neuronal Apoptosis-Inhibitory Protein
epithelial cells
Cell biology
Colorectal Neoplasms
host–pathogen interactions
medicine.drug
Subjects
Details
- ISSN :
- 14708752 and 03005127
- Volume :
- 49
- Database :
- OpenAIRE
- Journal :
- Biochemical Society Transactions
- Accession number :
- edsair.doi.dedup.....3e37795ebd4d71c7990e571ba712e810
- Full Text :
- https://doi.org/10.1042/bst20210365