Loading…

The mechanisms of NLRP3 inflammasome/pyroptosis activation and their role in diabetic retinopathy

In the working-age population worldwide, diabetic retinopathy (DR), a prevalent complication of diabetes, is the main cause of vision impairment. Chronic low-grade inflammation plays an essential role in DR development. Recently, concerning the pathogenesis of DR, the Nod-Like Receptor Family Pyrin...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in immunology 2023-04, Vol.14, p.1151185-1151185
Main Authors: Zheng, Xiaoqin, Wan, Jia, Tan, Gang
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c469t-ab966c3ff85f8f56508e7a33815a7e4ba85bb3c32d52ae6609e079d3add3c7763
cites cdi_FETCH-LOGICAL-c469t-ab966c3ff85f8f56508e7a33815a7e4ba85bb3c32d52ae6609e079d3add3c7763
container_end_page 1151185
container_issue
container_start_page 1151185
container_title Frontiers in immunology
container_volume 14
creator Zheng, Xiaoqin
Wan, Jia
Tan, Gang
description In the working-age population worldwide, diabetic retinopathy (DR), a prevalent complication of diabetes, is the main cause of vision impairment. Chronic low-grade inflammation plays an essential role in DR development. Recently, concerning the pathogenesis of DR, the Nod-Like Receptor Family Pyrin Domain Containing 3 (NLRP3) inflammasome in retinal cells has been determined as a causal factor. In the diabetic eye, the NLRP3 inflammasome is activated by several pathways (such as ROS and ATP). The activation of NPRP3 leads to the secretion of inflammatory cytokines interleukin-1β (IL-1β) and interleukin-18 (IL-18), and leads to pyroptosis, a rapid inflammatory form of lytic programmed cell death (PCD). Cells that undergo pyroptosis swell and rapture, releasing more inflammatory factors and accelerating DR progression. This review focuses on the mechanisms that activate NLRP3 inflammasome and pyroptosis leading to DR. The present research highlighted some inhibitors of NLRP3/pyroptosis pathways and novel therapeutic measures concerning DR treatment.
doi_str_mv 10.3389/fimmu.2023.1151185
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_e9fc2c12254945fbb61fcb3623a77b89</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_e9fc2c12254945fbb61fcb3623a77b89</doaj_id><sourcerecordid>2813560051</sourcerecordid><originalsourceid>FETCH-LOGICAL-c469t-ab966c3ff85f8f56508e7a33815a7e4ba85bb3c32d52ae6609e079d3add3c7763</originalsourceid><addsrcrecordid>eNpVkV1PHCEUhidNTTXqH-hFw2VvduVjgJmrpjH9MNnYxug1OTAHBzMMU5g12X_f0V2NcgEEzvtwyFNVnxldC9G0Fz7EuF1zysWaMclYIz9UJ0ypeiU4rz--2R9X56U80GXUrRBCfqqOhWYNZUydVHDbI4noehhDiYUkT643N38FCaMfIEYoKeLFtMtpmlMJhYCbwyPMIY0Exo7MPYZMchpwSZAugMU5OJKXeUwTzP3urDryMBQ8P6yn1d3PH7eXv1ebP7-uLr9vVq5W7bwC2yrlhPeN9I2XStIGNSxfZRI01hYaaa1wgneSAypFW6S67QR0nXBaK3FaXe25XYIHM-UQIe9MgmCeD1K-N5CX3gY02HrHHeNc1m0tvbWKeWeF4gK0tk27sL7tWdPWRuwcjnOG4R30_c0YenOfHg2jTGnK9UL4eiDk9G-LZTYxFIfDACOmbTG8YUIqSiVbSvm-1OVUSkb_-g6j5sm1eXZtnlybg-sl9OVth6-RF7PiP6P1p9M</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2813560051</pqid></control><display><type>article</type><title>The mechanisms of NLRP3 inflammasome/pyroptosis activation and their role in diabetic retinopathy</title><source>PubMed Central</source><creator>Zheng, Xiaoqin ; Wan, Jia ; Tan, Gang</creator><creatorcontrib>Zheng, Xiaoqin ; Wan, Jia ; Tan, Gang</creatorcontrib><description>In the working-age population worldwide, diabetic retinopathy (DR), a prevalent complication of diabetes, is the main cause of vision impairment. Chronic low-grade inflammation plays an essential role in DR development. Recently, concerning the pathogenesis of DR, the Nod-Like Receptor Family Pyrin Domain Containing 3 (NLRP3) inflammasome in retinal cells has been determined as a causal factor. In the diabetic eye, the NLRP3 inflammasome is activated by several pathways (such as ROS and ATP). The activation of NPRP3 leads to the secretion of inflammatory cytokines interleukin-1β (IL-1β) and interleukin-18 (IL-18), and leads to pyroptosis, a rapid inflammatory form of lytic programmed cell death (PCD). Cells that undergo pyroptosis swell and rapture, releasing more inflammatory factors and accelerating DR progression. This review focuses on the mechanisms that activate NLRP3 inflammasome and pyroptosis leading to DR. The present research highlighted some inhibitors of NLRP3/pyroptosis pathways and novel therapeutic measures concerning DR treatment.</description><identifier>ISSN: 1664-3224</identifier><identifier>EISSN: 1664-3224</identifier><identifier>DOI: 10.3389/fimmu.2023.1151185</identifier><identifier>PMID: 37180116</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>Apoptosis ; Diabetes Mellitus ; diabetic retinopathy ; Diabetic Retinopathy - etiology ; Diabetic Retinopathy - metabolism ; Humans ; Immunology ; Inflammasomes - metabolism ; Inflammation ; NLR Family, Pyrin Domain-Containing 3 Protein - metabolism ; NLRP3 ; pyroptosis ; Pyroptosis - physiology ; treatments</subject><ispartof>Frontiers in immunology, 2023-04, Vol.14, p.1151185-1151185</ispartof><rights>Copyright © 2023 Zheng, Wan and Tan.</rights><rights>Copyright © 2023 Zheng, Wan and Tan 2023 Zheng, Wan and Tan</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-ab966c3ff85f8f56508e7a33815a7e4ba85bb3c32d52ae6609e079d3add3c7763</citedby><cites>FETCH-LOGICAL-c469t-ab966c3ff85f8f56508e7a33815a7e4ba85bb3c32d52ae6609e079d3add3c7763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167027/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167027/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37180116$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zheng, Xiaoqin</creatorcontrib><creatorcontrib>Wan, Jia</creatorcontrib><creatorcontrib>Tan, Gang</creatorcontrib><title>The mechanisms of NLRP3 inflammasome/pyroptosis activation and their role in diabetic retinopathy</title><title>Frontiers in immunology</title><addtitle>Front Immunol</addtitle><description>In the working-age population worldwide, diabetic retinopathy (DR), a prevalent complication of diabetes, is the main cause of vision impairment. Chronic low-grade inflammation plays an essential role in DR development. Recently, concerning the pathogenesis of DR, the Nod-Like Receptor Family Pyrin Domain Containing 3 (NLRP3) inflammasome in retinal cells has been determined as a causal factor. In the diabetic eye, the NLRP3 inflammasome is activated by several pathways (such as ROS and ATP). The activation of NPRP3 leads to the secretion of inflammatory cytokines interleukin-1β (IL-1β) and interleukin-18 (IL-18), and leads to pyroptosis, a rapid inflammatory form of lytic programmed cell death (PCD). Cells that undergo pyroptosis swell and rapture, releasing more inflammatory factors and accelerating DR progression. This review focuses on the mechanisms that activate NLRP3 inflammasome and pyroptosis leading to DR. The present research highlighted some inhibitors of NLRP3/pyroptosis pathways and novel therapeutic measures concerning DR treatment.</description><subject>Apoptosis</subject><subject>Diabetes Mellitus</subject><subject>diabetic retinopathy</subject><subject>Diabetic Retinopathy - etiology</subject><subject>Diabetic Retinopathy - metabolism</subject><subject>Humans</subject><subject>Immunology</subject><subject>Inflammasomes - metabolism</subject><subject>Inflammation</subject><subject>NLR Family, Pyrin Domain-Containing 3 Protein - metabolism</subject><subject>NLRP3</subject><subject>pyroptosis</subject><subject>Pyroptosis - physiology</subject><subject>treatments</subject><issn>1664-3224</issn><issn>1664-3224</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkV1PHCEUhidNTTXqH-hFw2VvduVjgJmrpjH9MNnYxug1OTAHBzMMU5g12X_f0V2NcgEEzvtwyFNVnxldC9G0Fz7EuF1zysWaMclYIz9UJ0ypeiU4rz--2R9X56U80GXUrRBCfqqOhWYNZUydVHDbI4noehhDiYUkT643N38FCaMfIEYoKeLFtMtpmlMJhYCbwyPMIY0Exo7MPYZMchpwSZAugMU5OJKXeUwTzP3urDryMBQ8P6yn1d3PH7eXv1ebP7-uLr9vVq5W7bwC2yrlhPeN9I2XStIGNSxfZRI01hYaaa1wgneSAypFW6S67QR0nXBaK3FaXe25XYIHM-UQIe9MgmCeD1K-N5CX3gY02HrHHeNc1m0tvbWKeWeF4gK0tk27sL7tWdPWRuwcjnOG4R30_c0YenOfHg2jTGnK9UL4eiDk9G-LZTYxFIfDACOmbTG8YUIqSiVbSvm-1OVUSkb_-g6j5sm1eXZtnlybg-sl9OVth6-RF7PiP6P1p9M</recordid><startdate>20230425</startdate><enddate>20230425</enddate><creator>Zheng, Xiaoqin</creator><creator>Wan, Jia</creator><creator>Tan, Gang</creator><general>Frontiers Media S.A</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230425</creationdate><title>The mechanisms of NLRP3 inflammasome/pyroptosis activation and their role in diabetic retinopathy</title><author>Zheng, Xiaoqin ; Wan, Jia ; Tan, Gang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-ab966c3ff85f8f56508e7a33815a7e4ba85bb3c32d52ae6609e079d3add3c7763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Apoptosis</topic><topic>Diabetes Mellitus</topic><topic>diabetic retinopathy</topic><topic>Diabetic Retinopathy - etiology</topic><topic>Diabetic Retinopathy - metabolism</topic><topic>Humans</topic><topic>Immunology</topic><topic>Inflammasomes - metabolism</topic><topic>Inflammation</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein - metabolism</topic><topic>NLRP3</topic><topic>pyroptosis</topic><topic>Pyroptosis - physiology</topic><topic>treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Xiaoqin</creatorcontrib><creatorcontrib>Wan, Jia</creatorcontrib><creatorcontrib>Tan, Gang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Xiaoqin</au><au>Wan, Jia</au><au>Tan, Gang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The mechanisms of NLRP3 inflammasome/pyroptosis activation and their role in diabetic retinopathy</atitle><jtitle>Frontiers in immunology</jtitle><addtitle>Front Immunol</addtitle><date>2023-04-25</date><risdate>2023</risdate><volume>14</volume><spage>1151185</spage><epage>1151185</epage><pages>1151185-1151185</pages><issn>1664-3224</issn><eissn>1664-3224</eissn><abstract>In the working-age population worldwide, diabetic retinopathy (DR), a prevalent complication of diabetes, is the main cause of vision impairment. Chronic low-grade inflammation plays an essential role in DR development. Recently, concerning the pathogenesis of DR, the Nod-Like Receptor Family Pyrin Domain Containing 3 (NLRP3) inflammasome in retinal cells has been determined as a causal factor. In the diabetic eye, the NLRP3 inflammasome is activated by several pathways (such as ROS and ATP). The activation of NPRP3 leads to the secretion of inflammatory cytokines interleukin-1β (IL-1β) and interleukin-18 (IL-18), and leads to pyroptosis, a rapid inflammatory form of lytic programmed cell death (PCD). Cells that undergo pyroptosis swell and rapture, releasing more inflammatory factors and accelerating DR progression. This review focuses on the mechanisms that activate NLRP3 inflammasome and pyroptosis leading to DR. The present research highlighted some inhibitors of NLRP3/pyroptosis pathways and novel therapeutic measures concerning DR treatment.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>37180116</pmid><doi>10.3389/fimmu.2023.1151185</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1664-3224
ispartof Frontiers in immunology, 2023-04, Vol.14, p.1151185-1151185
issn 1664-3224
1664-3224
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_e9fc2c12254945fbb61fcb3623a77b89
source PubMed Central
subjects Apoptosis
Diabetes Mellitus
diabetic retinopathy
Diabetic Retinopathy - etiology
Diabetic Retinopathy - metabolism
Humans
Immunology
Inflammasomes - metabolism
Inflammation
NLR Family, Pyrin Domain-Containing 3 Protein - metabolism
NLRP3
pyroptosis
Pyroptosis - physiology
treatments
title The mechanisms of NLRP3 inflammasome/pyroptosis activation and their role in diabetic retinopathy
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T22%3A35%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20mechanisms%20of%20NLRP3%20inflammasome/pyroptosis%20activation%20and%20their%20role%20in%20diabetic%20retinopathy&rft.jtitle=Frontiers%20in%20immunology&rft.au=Zheng,%20Xiaoqin&rft.date=2023-04-25&rft.volume=14&rft.spage=1151185&rft.epage=1151185&rft.pages=1151185-1151185&rft.issn=1664-3224&rft.eissn=1664-3224&rft_id=info:doi/10.3389/fimmu.2023.1151185&rft_dat=%3Cproquest_doaj_%3E2813560051%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c469t-ab966c3ff85f8f56508e7a33815a7e4ba85bb3c32d52ae6609e079d3add3c7763%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2813560051&rft_id=info:pmid/37180116&rfr_iscdi=true