| Literature DB >> 24411941 |
Sebastian C Hasenfuss1, Latifa Bakiri2, Martin K Thomsen2, Evan G Williams3, Johan Auwerx3, Erwin F Wagner4.
Abstract
Nonalcoholic fatty liver disease (NAFLD) affects up to 30% of the adult population in Western societies, yet the underlying molecular pathways remain poorly understood. Here, we identify the dimeric Activator Protein 1 as a regulator of NAFLD. Fos-related antigen 1 (Fra-1) and Fos-related antigen 2 (Fra-2) prevent dietary NAFLD by inhibiting prosteatotic PPARγ signaling. Moreover, established NAFLD and the associated liver damage can be efficiently reversed by hepatocyte-specific Fra-1 expression. In contrast, c-Fos promotes PPARγ expression, while c-Jun exerts opposing, dimer-dependent functions. Interestingly, JunD was found to be essential for PPARγ signaling and NAFLD development. This unique antagonistic regulation of PPARγ by distinct AP-1 dimers occurs at the transcriptional level and establishes AP-1 as a link between obesity, hepatic lipid metabolism, and NAFLD.Entities:
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Year: 2014 PMID: 24411941 PMCID: PMC4023468 DOI: 10.1016/j.cmet.2013.11.018
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287