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http://purl.uniprot.org/citations/36253358http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/36253358http://www.w3.org/2000/01/rdf-schema#comment"Renal fibrosis is a common pathological feature and outcome of almost all chronic kidney diseases, and it is characterized by metabolic reprogramming toward aerobic glycolysis. Mesenchymal stem cell-derived exosomes (MSC-Exos) have been proposed as a promising therapeutic approach for renal fibrosis. In this study, we investigated the effect of MSC-Exos on glycolysis and the underlying mechanisms. We demonstrated that MSC-Exos significantly ameliorated unilateral ureter obstruction (UUO)-induced renal fibrosis by inhibiting glycolysis in tubular epithelial cells (TECs). miRNA sequencing showed that miR-21a-5p was highly enriched in MSC-Exos. Mechanistically, miR-21a-5p repressed the expression of phosphofructokinase muscle isoform (PFKM), a rate-limiting enzyme of glycolysis, thereby attenuating glycolysis in TECs. Additionally, knockdown of miR-21a-5p abolished the renoprotective effect of MSC-Exos. These findings revealed a novel role for MSC-Exos in the suppression of glycolysis, providing a new insight into the treatment of renal fibrosis."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.org/dc/terms/identifier"doi:10.1038/s41419-022-05305-7"xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Chen J."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Dong L."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Cao Y."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Chen T."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Guo J."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Jia Y."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Luo Y."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Shi Y."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Zhang Y."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Xu S."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Rong R."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/author"Cheuk Y.C."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/name"Cell Death Dis"xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/pages"876"xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/title"Bone marrow mesenchymal stem cell-derived exosomal miR-21a-5p alleviates renal fibrosis by attenuating glycolysis by targeting PFKM."xsd:string
http://purl.uniprot.org/citations/36253358http://purl.uniprot.org/core/volume"13"xsd:string
http://purl.uniprot.org/citations/36253358http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/36253358
http://purl.uniprot.org/citations/36253358http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/36253358
http://purl.uniprot.org/uniprot/#_A0A024R0Y5-mappedCitation-36253358http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36253358
http://purl.uniprot.org/uniprot/#_A0A2R8Y891-mappedCitation-36253358http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36253358
http://purl.uniprot.org/uniprot/#_A0A0S2Z4A1-mappedCitation-36253358http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36253358