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NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection
The innate immune system relies on families of pattern recognition receptors (PRRs) that detect distinct conserved molecular motifs from microbes to initiate antimicrobial responses. Activation of PRRs triggers a series of signaling cascades, leading to the release of pro-inflammatory cytokines, che...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268748/ https://www.ncbi.nlm.nih.gov/pubmed/34201509 http://dx.doi.org/10.3390/ijms22136714 |
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author | Pei, Gang Dorhoi, Anca |
author_facet | Pei, Gang Dorhoi, Anca |
author_sort | Pei, Gang |
collection | PubMed |
description | The innate immune system relies on families of pattern recognition receptors (PRRs) that detect distinct conserved molecular motifs from microbes to initiate antimicrobial responses. Activation of PRRs triggers a series of signaling cascades, leading to the release of pro-inflammatory cytokines, chemokines and antimicrobials, thereby contributing to the early host defense against microbes and regulating adaptive immunity. Additionally, PRRs can detect perturbation of cellular homeostasis caused by pathogens and fine-tune the immune responses. Among PRRs, nucleotide binding oligomerization domain (NOD)-like receptors (NLRs) have attracted particular interest in the context of cellular stress-induced inflammation during infection. Recently, mechanistic insights into the monitoring of cellular homeostasis perturbation by NLRs have been provided. We summarize the current knowledge about the disruption of cellular homeostasis by pathogens and focus on NLRs as innate immune sensors for its detection. We highlight the mechanisms employed by various pathogens to elicit cytoskeleton disruption, organelle stress as well as protein translation block, point out exemplary NLRs that guard cellular homeostasis during infection and introduce the concept of stress-associated molecular patterns (SAMPs). We postulate that integration of information about microbial patterns, danger signals, and SAMPs enables the innate immune system with adequate plasticity and precision in elaborating responses to microbes of variable virulence. |
format | Online Article Text |
id | pubmed-8268748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82687482021-07-10 NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection Pei, Gang Dorhoi, Anca Int J Mol Sci Review The innate immune system relies on families of pattern recognition receptors (PRRs) that detect distinct conserved molecular motifs from microbes to initiate antimicrobial responses. Activation of PRRs triggers a series of signaling cascades, leading to the release of pro-inflammatory cytokines, chemokines and antimicrobials, thereby contributing to the early host defense against microbes and regulating adaptive immunity. Additionally, PRRs can detect perturbation of cellular homeostasis caused by pathogens and fine-tune the immune responses. Among PRRs, nucleotide binding oligomerization domain (NOD)-like receptors (NLRs) have attracted particular interest in the context of cellular stress-induced inflammation during infection. Recently, mechanistic insights into the monitoring of cellular homeostasis perturbation by NLRs have been provided. We summarize the current knowledge about the disruption of cellular homeostasis by pathogens and focus on NLRs as innate immune sensors for its detection. We highlight the mechanisms employed by various pathogens to elicit cytoskeleton disruption, organelle stress as well as protein translation block, point out exemplary NLRs that guard cellular homeostasis during infection and introduce the concept of stress-associated molecular patterns (SAMPs). We postulate that integration of information about microbial patterns, danger signals, and SAMPs enables the innate immune system with adequate plasticity and precision in elaborating responses to microbes of variable virulence. MDPI 2021-06-23 /pmc/articles/PMC8268748/ /pubmed/34201509 http://dx.doi.org/10.3390/ijms22136714 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Pei, Gang Dorhoi, Anca NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection |
title | NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection |
title_full | NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection |
title_fullStr | NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection |
title_full_unstemmed | NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection |
title_short | NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection |
title_sort | nod-like receptors: guards of cellular homeostasis perturbation during infection |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268748/ https://www.ncbi.nlm.nih.gov/pubmed/34201509 http://dx.doi.org/10.3390/ijms22136714 |
work_keys_str_mv | AT peigang nodlikereceptorsguardsofcellularhomeostasisperturbationduringinfection AT dorhoianca nodlikereceptorsguardsofcellularhomeostasisperturbationduringinfection |