Meng Luke, Quezada Morgan, Levine Phillip, Han Yuyan, McDaniel Kelly, Zhou Tianhao, Lin Emily, Glaser Shannon, Meng Fanyin, Francis Heather, Alpini Gianfranco
Department of Research, Central Texas Veterans Health Care System, Temple, Texas; Department of Medicine, Digestive Disease Research Center, Scott & White Healthcare, Texas A&M Health Science Center, College of Medicine, Baylor Scott & White Health, Temple, Texas; Doctor of Medicine Program, University of Texas Southwestern Medical Center, Dallas, Texas.
Department of Medicine, Digestive Disease Research Center, Scott & White Healthcare, Texas A&M Health Science Center, College of Medicine, Baylor Scott & White Health, Temple, Texas.
Am J Pathol. 2015 Mar;185(3):602-9. doi: 10.1016/j.ajpath.2014.10.027. Epub 2015 Jan 22.
Cellular senescence is a state of irreversible cell cycle arrest that has been involved in many gastrointestinal diseases, including human cholestatic liver disorders. Senescence may play a role in biliary atresia, primary sclerosing cholangitis, cellular rejection, and primary biliary cirrhosis, four liver diseases affecting cholangiocytes and the biliary system. In this review, we examine proposed mechanisms of senescence-related biliary diseases, including hypotheses associated with the senescence-associated phenotype, induction of senescence in nearby cells, and the depletion of stem cell subpopulations. Current evidence for the molecular mechanisms of senescence in the previously mentioned diseases is discussed in detail, with attention to recent advances on the role of pathways associated with senescence-associated phenotype, stress-induced senescence, telomere dysfunction, and autophagy.
细胞衰老一种不可逆的细胞周期停滞状态,它与许多胃肠道疾病有关,包括人类胆汁淤积性肝病。衰老可能在胆道闭锁、原发性硬化性胆管炎、细胞排斥反应和原发性胆汁性肝硬化这四种影响胆管细胞和胆道系统的肝脏疾病中起作用。在这篇综述中,我们研究了衰老相关胆道疾病的潜在机制,包括与衰老相关表型、邻近细胞衰老的诱导以及干细胞亚群耗竭相关的假说。详细讨论了上述疾病中衰老分子机制的现有证据,重点关注与衰老相关表型、应激诱导衰老、端粒功能障碍和自噬相关途径作用的最新进展。