2022
DOI: 10.1007/s00281-022-00909-9
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Cellular senescence in the cholangiopathies: a driver of immunopathology and a novel therapeutic target

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Cited by 21 publications
(22 citation statements)
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“…During chronic senescence, the surrounding tissues are susceptible to senescence associated secretory phenotype (SASP) related damage, resulting in persistent inflammatory and fibrosis responses. Moreover, destructive SASP not only maintains the inflammatory response, but can also activate the senescent phenotype in surrounding non-senescent cells [ 201 ].…”
Section: Primary Sclerosing Cholangitismentioning
confidence: 99%
“…During chronic senescence, the surrounding tissues are susceptible to senescence associated secretory phenotype (SASP) related damage, resulting in persistent inflammatory and fibrosis responses. Moreover, destructive SASP not only maintains the inflammatory response, but can also activate the senescent phenotype in surrounding non-senescent cells [ 201 ].…”
Section: Primary Sclerosing Cholangitismentioning
confidence: 99%
“…Overactivation of the Notch signaling pathway was found in both diseases, further indicating aberrant biliary repair conditions ( 142 , 143 ). As immune-mediated diseases, the immune cells recruited by cholangiocyte secretion significantly altered the composition of intrahepatic immune cells and are involved in disease pathogenesis and regulation of biliary repair ( 144 ). ScRNA-seq of liver of PBC patients indicated that ORMDL3 + cholangiocytes displayed higher interaction with immune cells such as macrophages and monocytes, which might play a role in the pathogenesis of PBC ( 145 ).…”
Section: Role Of Immune Cells In Biliary Repair In Cholangiopathiesmentioning
confidence: 99%
“…58 In some mouse models of liver damage, senescent cells were shown to help reduce liver tissue injury and support a homeostatic environment while supporting the immune system. 58 However, when this phenotype persists, the cell experiences a chronic senescent state characterized by high levels of inflammation leading to fibrosis and cirrhosis. 57,58 This pathology is demonstrated in the proinflammatory environments of the PBC and PSC pathology.…”
Section: Heterogeneity In Response To Tissue Injurymentioning
confidence: 99%