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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...
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Published in: | Frontiers in immunology 2023-04, Vol.14, p.1151185-1151185 |
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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. |
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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> |
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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 |
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