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http://purl.uniprot.org/citations/37903776http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/37903776http://www.w3.org/2000/01/rdf-schema#comment"Insufficient pancreatic β-cell mass and reduced insulin expression are key events in the pathogenesis of diabetes mellitus (DM). Here we demonstrate the high expression of Talin-1 in β-cells and that deficiency of Talin-1 reduces β-cell proliferation, which leads to reduced β-cell mass and insulin expression, thus causing glucose intolerance without affecting peripheral insulin sensitivity in mice. High-fat diet fed exerbates these phenotypes. Mechanistically, Talin-1 interacts with the E3 ligase smad ubiquitination regulatory factor 1 (Smurf1), which prohibits ubiquitination of the signal transducer and activator of transcription 3 (Stat3) mediated by Smurf1, and ablation of Talin-1 enhances Smurf1-mediated ubiquitination of Stat3, leading to decreased β-cell proliferation and mass. Furthermore, haploinsufficiency of Talin-1 and Stat3 genes, but not that of either gene, in β-cell in mice significantly impairs glucose tolerance and insulin expression, indicating that both factors indeed function in the same genetic pathway. Finally, inducible deletion Talin-1 in β-cell causes glucose intolerance in adult mice. Collectively, our findings reveal that Talin-1 functions as a crucial regulator of β-cell mass, and highlight its potential as a therapeutic target for DM patients."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.org/dc/terms/identifier"doi:10.1038/s41419-023-06235-8"xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Cao H."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Chen L."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Chen Y."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Wu Y."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Tang W."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Yang H."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Yang D."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Zhou B."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Ding Z."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Hou X."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Ma G."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/author"Du C."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/name"Cell Death Dis"xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/pages"709"xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/title"Talin-1 inhibits Smurf1-mediated Stat3 degradation to modulate beta-cell proliferation and mass in mice."xsd:string
http://purl.uniprot.org/citations/37903776http://purl.uniprot.org/core/volume"14"xsd:string
http://purl.uniprot.org/citations/37903776http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/37903776
http://purl.uniprot.org/citations/37903776http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/37903776
http://purl.uniprot.org/uniprot/#_A0A0G2JEN5-mappedCitation-37903776http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37903776
http://purl.uniprot.org/uniprot/#_A2AIM2-mappedCitation-37903776http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37903776
http://purl.uniprot.org/uniprot/#_B7ZC18-mappedCitation-37903776http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37903776