Paracrine cellular senescence exacerbates biliary injury and impairs regeneration.

ABSTRACT: Cellular senescence is a mechanism that provides an irreversible barrier to cell cycle progression to prevent undesired proliferation. However, under pathological circumstances, senescence can adversely affect organ function, viability and regeneration. We have developed a mouse model of biliary senescence, based on the conditional deletion of Mdm2 in bile ducts under the control of the Krt19 promoter, that exhibits features of biliary disease. Here we report that senescent cholangiocytes induce profound alterations in the cellular and signalling microenvironment, with recruitment of myofibroblasts and macrophages causing collagen deposition, TGF? production and induction of senescence in surrounding cholangiocytes and hepatocytes. Finally, we study how inhibition of TGF?-signalling disrupts the transmission of senescence and restores liver function. We identify cellular senescence as a detrimental mechanism in the development of biliary injury. Our results identify TGF? as a potential therapeutic target to limit senescence-dependent aggravation in human cholangiopathies.

SUBMITTER: Ferreira-Gonzalez S 

PROVIDER: S-EPMC5844882 | biostudies-other | 2018 Mar

REPOSITORIES: biostudies-other