[No authors listed]
Mesencephalic astrocyteâderived neurotrophic factor (MANF) is an endoplasmic reticulum stressâinducible protein, which has been suggested to be upregulated in inflammatory diseases; however, how inflammation regulates its transcription remains unclear. Activator proteinâ1 (APâ1), which is a transcription factor complex composed of câFos and câJun, is activated during the inflammatory process. The present study aimed to investigate whether the APâ1 complex regulates MANF transcription. The results of a luciferase reporter assay revealed that one of three putative APâ1 binding sites in the MANF promoter region is essential for enhancement of MANF transcription. Mechanistically, APâ1 was revealed to directly bind to the promoter region of the MANF gene by chromatin immunoprecipitation assay. Furthermore, MANF was strongly expressed in the liver tissues of patients with hepatitis B virus (HBV) infection, compared with in normal liver tissues from patients with hepatic hemangioma. Furthermore, câFos and câJun were also upregulated in the nuclei of hepatocytes from patients with HBV infection. In mice treated with carbon tetrachloride, the expression patterns of MANF, câFos and câJun were similar to those in patients with HBV. These results suggested that the APâ1 complex may be a novel regulator of MANF transcription, which may be involved in liver inflammation and fibrosis.
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