{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Jalan-Sakrikar N"],"funding":["NCATS","NCATS NIH HHS","NIDDK NIH HHS","National Institutes of Health","NIDDK"],"pagination":["e170320"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10619490"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["8(20)"],"pubmed_abstract":["Cellular senescence and biliary fibrosis are prototypical features of obliterative cholangiopathies, such as primary sclerosing cholangitis (PSC). Telomere dysfunction can lead to senescence either through telomere erosion or damaged telomeres. Our goal was to investigate a mechanistic relationship between telomere damage and biliary fibrosis in PSC. Telomere attrition was observed in the bile ducts of patients with PSC along with a reduction in telomerase reverse transcriptase (TERT) expression, compared with that in normal livers. Similarly, liver tissue from mouse models of biliary fibrosis showed telomere attrition with increased damage at telomeres measured as telomere-associated foci (TAF). Cellular models of senescence induction increased the TAF in cholangiocytes. This coincided wi"],"journal":["JCI insight"],"pubmed_title":["Telomere dysfunction promotes cholangiocyte senescence and biliary fibrosis in primary sclerosing cholangitis."],"pmcid":["PMC10619490"],"funding_grant_id":["R01 DK117861","P30DK084567","P30 DK084567","KL2 TR002379","NIDDK","DK117861"],"pubmed_authors":["Gan C","Wixom AQ","Jurk D","Yaqoob U","Anwar A","Huebert RC","Jalan-Sakrikar N","Lagnado AB"],"additional_accession":[]},"is_claimable":false,"name":"Telomere dysfunction promotes cholangiocyte senescence and biliary fibrosis in primary sclerosing cholangitis.","description":"Cellular senescence and biliary fibrosis are prototypical features of obliterative cholangiopathies, such as primary sclerosing cholangitis (PSC). Telomere dysfunction can lead to senescence either through telomere erosion or damaged telomeres. Our goal was to investigate a mechanistic relationship between telomere damage and biliary fibrosis in PSC. Telomere attrition was observed in the bile ducts of patients with PSC along with a reduction in telomerase reverse transcriptase (TERT) expression, compared with that in normal livers. Similarly, liver tissue from mouse models of biliary fibrosis showed telomere attrition with increased damage at telomeres measured as telomere-associated foci (TAF). Cellular models of senescence induction increased the TAF in cholangiocytes. This coincided wi","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Oct","modification":"2026-05-29T12:18:17.509Z","creation":"2025-04-20T01:32:21.533Z"},"accession":"S-EPMC10619490","cross_references":{"pubmed":["37707950"],"doi":["10.1172/jci.insight.170320"]}}