A Novel Role for Tm7sf2 Gene in Regulating TNF alpha Expression

作者：Bellezza Ilaria^*; Roberti Rita; Gatticchi Leonardo; Del Sordo Rachele; Rambotti Maria Grazia; Marchetti Maria Cristina; Sidoni Angelo; Minelli Alba

来源：PLos One, 2013, 8(7): e68017.

DOI：10.1371/journal.pone.0068017

We have explored the role of Tm7sf2 gene, which codifies for 3 beta-hydroxysterol Delta 14-reductase, an endoplasmic reticulum resident protein, in the sensitivity to endoplasmic reticulum stress and in the resulting inflammatory response. We used mouse embryonic fibroblasts, derived from Tm7sf2(+/+) and Tm7sf2(-/-) mice, to determine the in vitro effects of thapsigargin on NF-kappa B activation. Our results show that the Tm7sf2 gene controls the launch of the unfolded protein response and presides an anti-inflammatory loop thus its absence correlates with NF-kappa B activation and TNF alpha up-regulation. Our data also show that Tm7sf2 gene regulates liver X receptor activation and its absence inhibits LXR signalling. By expressing the hTm7sf2 gene in KO MEFs and observing a reduced NF-kappa B activation, we have confirmed that Tm7sf2 gene is linked to NF-kappa B activation. Finally we used genetically modified mice in an in vivo model of ER stress and of inflammation. Our results show a significant increase in renal TNF alpha expression after tunicamycin exposure and in the oedematogenic response in Tm7sf2(-/-) mice. In conclusion, we have shown that the Tm7sf2 gene, to date involved only in cholesterol biosynthesis, also controls an anti-inflammatory loop thereby confirming the existence of cross talk between metabolic pathways and inflammatory response.