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http://purl.uniprot.org/citations/36822364http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/36822364http://www.w3.org/2000/01/rdf-schema#comment"Cystatin C has been linked to inflammation in other diseases, such as epilepsy and Alzheimer's disease. These studies were designed to investigate whether Cystatin C regulates retinal inflammation and permeability. To address this question, we used Cystatin C knockout mice in a retinal ischemia/reperfusion model to determine whether Cystatin C regulated retinal damage, as well as inflammatory mediators and retinal permeability. To support the mouse work, we also used primary retinal endothelial cells cultured in normal and high glucose. Ischemia/reperfusion in Cystatin C knockout mice caused increased formation of degenerate capillaries. Loss of Cystatin C increased fluorescein leakage in the retina, which was accompanied by reduced levels of zonula occludin 1 (ZO-1) and occludin proteins. When REC were grown in high glucose, recombinant Cystatin C decreased retinal permeability, while Cystatin C siRNA increased dextran flux compared to high glucose alone. Recombinant Cystatin C decreased levels of interleukin-1-beta (IL-1β) and high mobility group box 1 (HMGB1) levels. In conclusion, loss of Cystatin C increased vascular damage in response to ischemia/reperfusion. Cystatin C regulated permeability and inflammatory mediators in the retina in response to stressors. Cystatin C offers a new target for retinal disease therapeutic development."xsd:string
http://purl.uniprot.org/citations/36822364http://purl.org/dc/terms/identifier"doi:10.1016/j.mvr.2023.104510"xsd:string
http://purl.uniprot.org/citations/36822364http://purl.uniprot.org/core/author"Jiang Y."xsd:string
http://purl.uniprot.org/citations/36822364http://purl.uniprot.org/core/author"Liu L."xsd:string
http://purl.uniprot.org/citations/36822364http://purl.uniprot.org/core/author"Steinle J.J."xsd:string
http://purl.uniprot.org/citations/36822364http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/36822364http://purl.uniprot.org/core/name"Microvasc Res"xsd:string
http://purl.uniprot.org/citations/36822364http://purl.uniprot.org/core/pages"104510"xsd:string
http://purl.uniprot.org/citations/36822364http://purl.uniprot.org/core/title"Loss of cystatin C regulates permeability and inflammatory pathways in retina."xsd:string
http://purl.uniprot.org/citations/36822364http://purl.uniprot.org/core/volume"148"xsd:string
http://purl.uniprot.org/citations/36822364http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/36822364
http://purl.uniprot.org/citations/36822364http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/36822364
http://purl.uniprot.org/uniprot/#_P21460-mappedCitation-36822364http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36822364
http://purl.uniprot.org/uniprot/#_Q3U5K7-mappedCitation-36822364http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36822364
http://purl.uniprot.org/uniprot/#_Q9EPX9-mappedCitation-36822364http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36822364
http://purl.uniprot.org/uniprot/Q3U5K7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/36822364
http://purl.uniprot.org/uniprot/Q9EPX9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/36822364
http://purl.uniprot.org/uniprot/P21460http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/36822364