Role of Porphyromonas gingivalis in the downregulation of NLRp3 inflammasome in periodontitis

The innate immune response is the body's first line of defense against pathogens. The innate immune system recognizes pathogens, including bacteria and viruses by engagement of the germline-encoded pattern recognition receptors (PRRs). There are five families of PRRs which are able to sense vas...

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Main Authors: Neelam Gavali, Amit Chaudhari, Pramod Waghmare, Yogesh Khadtare, Pooja Shendge, Shubhangi Wadgounkar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Journal of International Clinical Dental Research Organization
Subjects:
Online Access:http://www.jicdro.org/article.asp?issn=2231-0754;year=2022;volume=14;issue=2;spage=91;epage=95;aulast=Gavali
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author Neelam Gavali
Amit Chaudhari
Pramod Waghmare
Yogesh Khadtare
Pooja Shendge
Shubhangi Wadgounkar
author_facet Neelam Gavali
Amit Chaudhari
Pramod Waghmare
Yogesh Khadtare
Pooja Shendge
Shubhangi Wadgounkar
author_sort Neelam Gavali
collection DOAJ
description The innate immune response is the body's first line of defense against pathogens. The innate immune system recognizes pathogens, including bacteria and viruses by engagement of the germline-encoded pattern recognition receptors (PRRs). There are five families of PRRs which are able to sense vast families of microbial components, referred to as pathogen-associated molecular patterns and damage-associated molecular patterns (DAMPs), they are host cell components produced during inflammation or environmentally derived. Although PRRs are predominately expressed by innate immune cells, many of the PRRs are also found on other cells including epithelial, endothelial, and cells of the adaptive immune system. PRR engagement by its ligand induces downstream signaling cascades that induce multiple effects, including activation of innate immune cells and cytokine/chemokine production for the recruitment of immune cells to the site of infection or tissue damage. There are multiple inflammasomes that are formed, which are named for their sensor PRR that induces its activation. It is still not clear how many sensors are capable of forming inflammasomes, with strong literature support for over 10 different inflammasomes, including NLRP1, NLRP3, NLRP6, NLRP12, pyrin, NAIP/NLRC4, RIG-I AIM2, IFI16, NLRC3, and NLP6 5,7 which are recently reviewed. The study of periodontal disease thus represents an excellent model to study the role of inflammasomes due to the abundance of Microbe Associated Molecular Patterns (MAMP) and DAMPs and the elevated proportion of macrophages in the tissue microenvironment.
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spelling doaj.art-470235f991c94057b641d3b03a3a0c8b2023-01-12T12:42:45ZengWolters Kluwer Medknow PublicationsJournal of International Clinical Dental Research Organization2231-07542022-01-01142919510.4103/jicdro.jicdro_37_21Role of Porphyromonas gingivalis in the downregulation of NLRp3 inflammasome in periodontitisNeelam GavaliAmit ChaudhariPramod WaghmareYogesh KhadtarePooja ShendgeShubhangi WadgounkarThe innate immune response is the body's first line of defense against pathogens. The innate immune system recognizes pathogens, including bacteria and viruses by engagement of the germline-encoded pattern recognition receptors (PRRs). There are five families of PRRs which are able to sense vast families of microbial components, referred to as pathogen-associated molecular patterns and damage-associated molecular patterns (DAMPs), they are host cell components produced during inflammation or environmentally derived. Although PRRs are predominately expressed by innate immune cells, many of the PRRs are also found on other cells including epithelial, endothelial, and cells of the adaptive immune system. PRR engagement by its ligand induces downstream signaling cascades that induce multiple effects, including activation of innate immune cells and cytokine/chemokine production for the recruitment of immune cells to the site of infection or tissue damage. There are multiple inflammasomes that are formed, which are named for their sensor PRR that induces its activation. It is still not clear how many sensors are capable of forming inflammasomes, with strong literature support for over 10 different inflammasomes, including NLRP1, NLRP3, NLRP6, NLRP12, pyrin, NAIP/NLRC4, RIG-I AIM2, IFI16, NLRC3, and NLP6 5,7 which are recently reviewed. The study of periodontal disease thus represents an excellent model to study the role of inflammasomes due to the abundance of Microbe Associated Molecular Patterns (MAMP) and DAMPs and the elevated proportion of macrophages in the tissue microenvironment.http://www.jicdro.org/article.asp?issn=2231-0754;year=2022;volume=14;issue=2;spage=91;epage=95;aulast=Gavaliinflammasomenlrp3 inflammasomeporphyromonas gingivalis
spellingShingle Neelam Gavali
Amit Chaudhari
Pramod Waghmare
Yogesh Khadtare
Pooja Shendge
Shubhangi Wadgounkar
Role of Porphyromonas gingivalis in the downregulation of NLRp3 inflammasome in periodontitis
Journal of International Clinical Dental Research Organization
inflammasome
nlrp3 inflammasome
porphyromonas gingivalis
title Role of Porphyromonas gingivalis in the downregulation of NLRp3 inflammasome in periodontitis
title_full Role of Porphyromonas gingivalis in the downregulation of NLRp3 inflammasome in periodontitis
title_fullStr Role of Porphyromonas gingivalis in the downregulation of NLRp3 inflammasome in periodontitis
title_full_unstemmed Role of Porphyromonas gingivalis in the downregulation of NLRp3 inflammasome in periodontitis
title_short Role of Porphyromonas gingivalis in the downregulation of NLRp3 inflammasome in periodontitis
title_sort role of porphyromonas gingivalis in the downregulation of nlrp3 inflammasome in periodontitis
topic inflammasome
nlrp3 inflammasome
porphyromonas gingivalis
url http://www.jicdro.org/article.asp?issn=2231-0754;year=2022;volume=14;issue=2;spage=91;epage=95;aulast=Gavali
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