Internal medicine

Protein kinase R

Liver disease

Alcoholic liver disease

ATF6

Disease

Biology

Endoplasmic reticulum

Unfolded protein response

Kinase

Immunology

Cirrhosis

EIF-2 kinase

Fatty liver

Signal transduction

Activating transcription factor

Mitogen-activated protein kinase kinase

Cell biology

Protein kinase A

Cancer research

Medicine

Cyclin-dependent kinase 2

Liver Research

Endoplasmic reticulum (ER) stress occurs when ER homeostasis is perturbed with accumulation of unfolded/misfolded protein or calcium depletion. The unfolded protein response (UPR), comprising of inositol-requiring enzyme 1α (IRE1α), PKR-like ER kinase (PERK) and activating transcription factor 6 (ATF6) signaling pathways, is a protective cellular response activated by ER stress. However, UPR activation can also induce cell death upon persistent ER stress. The liver is susceptible to ER stress given its synthetic and other biological functions. Numerous studies from human liver samples and animal disease models have indicated a crucial role of ER stress and UPR signaling pathways in the pathogenesis of liver diseases, including non-alcoholic fatty liver disease, alcoholic liver disease, alpha-1 antitrypsin deficiency, cholestatic liver disease, drug-induced liver injury, ischemia/reperfusion injury, viral hepatitis and hepatocellular carcinoma. Extensive investigations have demonstrated the potential underlying mechanisms of the induction of ER stress and the contribution of UPR pathways during the development of the diseases. Moreover ER stress and the UPR proteins and genes have become emerging therapeutic targets to treat liver diseases.

Endoplasmic reticulum stress and liver diseases