GSDMD-mediated pyroptosis in retinal vascular inflammatory diseases: a review
Purpose Pyroptosis is a newly discovered form of programmed pro-inflammatory cell death. The main signaling pathways include the classical scorch death pathway that depends on NLRP3 inflammatory vesicles and other activation caspase-1 and the non-classical scorch death pathway that depends on caspas...
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| Veröffentlicht in: | International ophthalmology 2023-04, Vol.43 (4), p.1405-1411 |
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| creator | Xiaodong, Li Xuejun, Xie |
| description | Purpose
Pyroptosis is a newly discovered form of programmed pro-inflammatory cell death. The main signaling pathways include the classical scorch death pathway that depends on NLRP3 inflammatory vesicles and other activation caspase-1 and the non-classical scorch death pathway that depends on caspase-4 /5/11. The substrate of all inflammatory caspases is GSDMD; a large number of studies have confirmed that pyroptosis is associated with certain infectious diseases, atherosclerotic diseases, metabolic diseases, and aseptic inflammatory diseases of important organs. In recent years, pyroptosis has been studied partially in the ocular field. So, this article reviews the recent literature intending to help readers understand the main mechanisms of cellular scorch death and the progress of GSDMD-mediated cellular scorch death in retinal vascular inflammatory diseases.
Method
A detailed review of the literature related to pyroptosis and inflammatory diseases of the retinal vasculature is presented. The following 6 electronic databases were searched: CNKI, Wanfang, VIP, PubMed, The Cochrane Library, and Embase Databases, and the search period was from the database to May 2022. The main search keywords include “Pyroptosis,” “ GSDMD,” “Retinal Vascular Inflammatory Disease,” “Diabetic retinopathy,” “Retinal vasculitis.” The discovery of pyroptosis, the main molecular mechanisms, key proteins, and their pathogenesis and therapeutic prospects in retinal vasculitis diseases are extensively studied and summarized.
Result
The mechanisms of gasdermin D-mediated pyroptosis are elaborated and analyzed, with particular emphasis on their key role and potential in the pathogenesis and treatment of inflammatory retinal vascular lesions.
Conclusion
Gasdermin D-mediated pyroptosis is a well-studied form of programmed pro-inflammatory cell death, which has a bidirectional regulatory effect on a variety of immune and inflammatory diseases. The literature reveals that pyroptosis is closely related to the pathogenesis of retinal vascular inflammatory diseases, and it may be an important therapeutic target for diabetic retinopathy and other retinal vasculitis eye diseases in the future. |
| doi_str_mv | 10.1007/s10792-022-02506-z |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2711308044</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2711308044</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-7154c2aa12ed967d062a46c22eaeb367df9f0a2e1e9e14ba708a6f87a40b7f603</originalsourceid><addsrcrecordid>eNp9kD1PwzAQhi0E4vsPMKBILCyBs53YMRtqoSBRMQCzdU0uKFXSFDsBlV-PS8uHGBiss-6eey0_jB1xOOMA-txz0EbEIJYnBRW_b7BdnmoZCyVh89d9h-15PwUAo43aZjtSgcqkMbtsPHoYjodxQ0WFHRXRfOHaedf6ykfVLHLUVTOso1f0eV-jC72yxqbBrnWLqKg8oSd_EWEgXyt6O2BbJdaeDtd1nz1dXz0ObuK7-9Ht4PIuzqVOu1jzNMkFIhdUGKULUAITlQtBSBMZGqUpAQVxMsSTCWrIUJWZxgQmulQg99npKnfu2peefGebyudU1zijtvdWaM4lZJAkAT35g07b3oVPBSoDoVKTJiZQYkXlrvXeUWnnrmrQLSwHu5RtV7JtkG0_Zdv3sHS8ju4nQeD3ypfdAMgV4MNo9kzu5-1_Yj8AHWaKVA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2802659549</pqid></control><display><type>article</type><title>GSDMD-mediated pyroptosis in retinal vascular inflammatory diseases: a review</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Xiaodong, Li ; Xuejun, Xie</creator><creatorcontrib>Xiaodong, Li ; Xuejun, Xie</creatorcontrib><description>Purpose
Pyroptosis is a newly discovered form of programmed pro-inflammatory cell death. The main signaling pathways include the classical scorch death pathway that depends on NLRP3 inflammatory vesicles and other activation caspase-1 and the non-classical scorch death pathway that depends on caspase-4 /5/11. The substrate of all inflammatory caspases is GSDMD; a large number of studies have confirmed that pyroptosis is associated with certain infectious diseases, atherosclerotic diseases, metabolic diseases, and aseptic inflammatory diseases of important organs. In recent years, pyroptosis has been studied partially in the ocular field. So, this article reviews the recent literature intending to help readers understand the main mechanisms of cellular scorch death and the progress of GSDMD-mediated cellular scorch death in retinal vascular inflammatory diseases.
Method
A detailed review of the literature related to pyroptosis and inflammatory diseases of the retinal vasculature is presented. The following 6 electronic databases were searched: CNKI, Wanfang, VIP, PubMed, The Cochrane Library, and Embase Databases, and the search period was from the database to May 2022. The main search keywords include “Pyroptosis,” “ GSDMD,” “Retinal Vascular Inflammatory Disease,” “Diabetic retinopathy,” “Retinal vasculitis.” The discovery of pyroptosis, the main molecular mechanisms, key proteins, and their pathogenesis and therapeutic prospects in retinal vasculitis diseases are extensively studied and summarized.
Result
The mechanisms of gasdermin D-mediated pyroptosis are elaborated and analyzed, with particular emphasis on their key role and potential in the pathogenesis and treatment of inflammatory retinal vascular lesions.
Conclusion
Gasdermin D-mediated pyroptosis is a well-studied form of programmed pro-inflammatory cell death, which has a bidirectional regulatory effect on a variety of immune and inflammatory diseases. The literature reveals that pyroptosis is closely related to the pathogenesis of retinal vascular inflammatory diseases, and it may be an important therapeutic target for diabetic retinopathy and other retinal vasculitis eye diseases in the future.</description><identifier>ISSN: 1573-2630</identifier><identifier>ISSN: 0165-5701</identifier><identifier>EISSN: 1573-2630</identifier><identifier>DOI: 10.1007/s10792-022-02506-z</identifier><identifier>PMID: 36068399</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Apoptosis ; Arteriosclerosis ; Atherosclerosis ; Caspase-1 ; Caspase-4 ; Caspases - metabolism ; Cell death ; Diabetes ; Diabetes mellitus ; Diabetic Retinopathy ; Eye diseases ; Gasdermins ; Humans ; Infectious diseases ; Inflammatory diseases ; Intracellular Signaling Peptides and Proteins - metabolism ; Literature reviews ; Medicine ; Medicine & Public Health ; Metabolic disorders ; Molecular modelling ; Mortality ; Neoplasm Proteins ; New Treatments for Keratoconus ; Ophthalmology ; Pathogenesis ; Phosphate-Binding Proteins - metabolism ; Pore Forming Cytotoxic Proteins - metabolism ; Pyroptosis ; Retina ; Retinal Vasculitis ; Retinopathy ; Review ; Scorch ; Substrates ; Therapeutic targets ; Vasculitis</subject><ispartof>International ophthalmology, 2023-04, Vol.43 (4), p.1405-1411</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2022. The Author(s), under exclusive licence to Springer Nature B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-7154c2aa12ed967d062a46c22eaeb367df9f0a2e1e9e14ba708a6f87a40b7f603</citedby><cites>FETCH-LOGICAL-c375t-7154c2aa12ed967d062a46c22eaeb367df9f0a2e1e9e14ba708a6f87a40b7f603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10792-022-02506-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10792-022-02506-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36068399$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xiaodong, Li</creatorcontrib><creatorcontrib>Xuejun, Xie</creatorcontrib><title>GSDMD-mediated pyroptosis in retinal vascular inflammatory diseases: a review</title><title>International ophthalmology</title><addtitle>Int Ophthalmol</addtitle><addtitle>Int Ophthalmol</addtitle><description>Purpose
Pyroptosis is a newly discovered form of programmed pro-inflammatory cell death. The main signaling pathways include the classical scorch death pathway that depends on NLRP3 inflammatory vesicles and other activation caspase-1 and the non-classical scorch death pathway that depends on caspase-4 /5/11. The substrate of all inflammatory caspases is GSDMD; a large number of studies have confirmed that pyroptosis is associated with certain infectious diseases, atherosclerotic diseases, metabolic diseases, and aseptic inflammatory diseases of important organs. In recent years, pyroptosis has been studied partially in the ocular field. So, this article reviews the recent literature intending to help readers understand the main mechanisms of cellular scorch death and the progress of GSDMD-mediated cellular scorch death in retinal vascular inflammatory diseases.
Method
A detailed review of the literature related to pyroptosis and inflammatory diseases of the retinal vasculature is presented. The following 6 electronic databases were searched: CNKI, Wanfang, VIP, PubMed, The Cochrane Library, and Embase Databases, and the search period was from the database to May 2022. The main search keywords include “Pyroptosis,” “ GSDMD,” “Retinal Vascular Inflammatory Disease,” “Diabetic retinopathy,” “Retinal vasculitis.” The discovery of pyroptosis, the main molecular mechanisms, key proteins, and their pathogenesis and therapeutic prospects in retinal vasculitis diseases are extensively studied and summarized.
Result
The mechanisms of gasdermin D-mediated pyroptosis are elaborated and analyzed, with particular emphasis on their key role and potential in the pathogenesis and treatment of inflammatory retinal vascular lesions.
Conclusion
Gasdermin D-mediated pyroptosis is a well-studied form of programmed pro-inflammatory cell death, which has a bidirectional regulatory effect on a variety of immune and inflammatory diseases. The literature reveals that pyroptosis is closely related to the pathogenesis of retinal vascular inflammatory diseases, and it may be an important therapeutic target for diabetic retinopathy and other retinal vasculitis eye diseases in the future.</description><subject>Apoptosis</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Caspase-1</subject><subject>Caspase-4</subject><subject>Caspases - metabolism</subject><subject>Cell death</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetic Retinopathy</subject><subject>Eye diseases</subject><subject>Gasdermins</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Inflammatory diseases</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Literature reviews</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic disorders</subject><subject>Molecular modelling</subject><subject>Mortality</subject><subject>Neoplasm Proteins</subject><subject>New Treatments for Keratoconus</subject><subject>Ophthalmology</subject><subject>Pathogenesis</subject><subject>Phosphate-Binding Proteins - metabolism</subject><subject>Pore Forming Cytotoxic Proteins - metabolism</subject><subject>Pyroptosis</subject><subject>Retina</subject><subject>Retinal Vasculitis</subject><subject>Retinopathy</subject><subject>Review</subject><subject>Scorch</subject><subject>Substrates</subject><subject>Therapeutic targets</subject><subject>Vasculitis</subject><issn>1573-2630</issn><issn>0165-5701</issn><issn>1573-2630</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kD1PwzAQhi0E4vsPMKBILCyBs53YMRtqoSBRMQCzdU0uKFXSFDsBlV-PS8uHGBiss-6eey0_jB1xOOMA-txz0EbEIJYnBRW_b7BdnmoZCyVh89d9h-15PwUAo43aZjtSgcqkMbtsPHoYjodxQ0WFHRXRfOHaedf6ykfVLHLUVTOso1f0eV-jC72yxqbBrnWLqKg8oSd_EWEgXyt6O2BbJdaeDtd1nz1dXz0ObuK7-9Ht4PIuzqVOu1jzNMkFIhdUGKULUAITlQtBSBMZGqUpAQVxMsSTCWrIUJWZxgQmulQg99npKnfu2peefGebyudU1zijtvdWaM4lZJAkAT35g07b3oVPBSoDoVKTJiZQYkXlrvXeUWnnrmrQLSwHu5RtV7JtkG0_Zdv3sHS8ju4nQeD3ypfdAMgV4MNo9kzu5-1_Yj8AHWaKVA</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Xiaodong, Li</creator><creator>Xuejun, Xie</creator><general>Springer Netherlands</general><general>Springer Nature B.V</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>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20230401</creationdate><title>GSDMD-mediated pyroptosis in retinal vascular inflammatory diseases: a review</title><author>Xiaodong, Li ; Xuejun, Xie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-7154c2aa12ed967d062a46c22eaeb367df9f0a2e1e9e14ba708a6f87a40b7f603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Apoptosis</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Caspase-1</topic><topic>Caspase-4</topic><topic>Caspases - metabolism</topic><topic>Cell death</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetic Retinopathy</topic><topic>Eye diseases</topic><topic>Gasdermins</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Inflammatory diseases</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Literature reviews</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic disorders</topic><topic>Molecular modelling</topic><topic>Mortality</topic><topic>Neoplasm Proteins</topic><topic>New Treatments for Keratoconus</topic><topic>Ophthalmology</topic><topic>Pathogenesis</topic><topic>Phosphate-Binding Proteins - metabolism</topic><topic>Pore Forming Cytotoxic Proteins - metabolism</topic><topic>Pyroptosis</topic><topic>Retina</topic><topic>Retinal Vasculitis</topic><topic>Retinopathy</topic><topic>Review</topic><topic>Scorch</topic><topic>Substrates</topic><topic>Therapeutic targets</topic><topic>Vasculitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiaodong, Li</creatorcontrib><creatorcontrib>Xuejun, Xie</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>International ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiaodong, Li</au><au>Xuejun, Xie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GSDMD-mediated pyroptosis in retinal vascular inflammatory diseases: a review</atitle><jtitle>International ophthalmology</jtitle><stitle>Int Ophthalmol</stitle><addtitle>Int Ophthalmol</addtitle><date>2023-04-01</date><risdate>2023</risdate><volume>43</volume><issue>4</issue><spage>1405</spage><epage>1411</epage><pages>1405-1411</pages><issn>1573-2630</issn><issn>0165-5701</issn><eissn>1573-2630</eissn><abstract>Purpose
Pyroptosis is a newly discovered form of programmed pro-inflammatory cell death. The main signaling pathways include the classical scorch death pathway that depends on NLRP3 inflammatory vesicles and other activation caspase-1 and the non-classical scorch death pathway that depends on caspase-4 /5/11. The substrate of all inflammatory caspases is GSDMD; a large number of studies have confirmed that pyroptosis is associated with certain infectious diseases, atherosclerotic diseases, metabolic diseases, and aseptic inflammatory diseases of important organs. In recent years, pyroptosis has been studied partially in the ocular field. So, this article reviews the recent literature intending to help readers understand the main mechanisms of cellular scorch death and the progress of GSDMD-mediated cellular scorch death in retinal vascular inflammatory diseases.
Method
A detailed review of the literature related to pyroptosis and inflammatory diseases of the retinal vasculature is presented. The following 6 electronic databases were searched: CNKI, Wanfang, VIP, PubMed, The Cochrane Library, and Embase Databases, and the search period was from the database to May 2022. The main search keywords include “Pyroptosis,” “ GSDMD,” “Retinal Vascular Inflammatory Disease,” “Diabetic retinopathy,” “Retinal vasculitis.” The discovery of pyroptosis, the main molecular mechanisms, key proteins, and their pathogenesis and therapeutic prospects in retinal vasculitis diseases are extensively studied and summarized.
Result
The mechanisms of gasdermin D-mediated pyroptosis are elaborated and analyzed, with particular emphasis on their key role and potential in the pathogenesis and treatment of inflammatory retinal vascular lesions.
Conclusion
Gasdermin D-mediated pyroptosis is a well-studied form of programmed pro-inflammatory cell death, which has a bidirectional regulatory effect on a variety of immune and inflammatory diseases. The literature reveals that pyroptosis is closely related to the pathogenesis of retinal vascular inflammatory diseases, and it may be an important therapeutic target for diabetic retinopathy and other retinal vasculitis eye diseases in the future.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>36068399</pmid><doi>10.1007/s10792-022-02506-z</doi><tpages>7</tpages></addata></record> |
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| subjects | Apoptosis Arteriosclerosis Atherosclerosis Caspase-1 Caspase-4 Caspases - metabolism Cell death Diabetes Diabetes mellitus Diabetic Retinopathy Eye diseases Gasdermins Humans Infectious diseases Inflammatory diseases Intracellular Signaling Peptides and Proteins - metabolism Literature reviews Medicine Medicine & Public Health Metabolic disorders Molecular modelling Mortality Neoplasm Proteins New Treatments for Keratoconus Ophthalmology Pathogenesis Phosphate-Binding Proteins - metabolism Pore Forming Cytotoxic Proteins - metabolism Pyroptosis Retina Retinal Vasculitis Retinopathy Review Scorch Substrates Therapeutic targets Vasculitis |
| title | GSDMD-mediated pyroptosis in retinal vascular inflammatory diseases: a review |
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