The Transcription Factor IRF6 Co-Represses PPAR?-Mediated Cytoprotection in Ischemic Cerebrovascular Endothelial Cells.

ABSTRACT: Activation of peroxisome proliferator-activated receptor gamma (PPAR?) in the cerebrovascular endothelium is a key suppressor of post-stroke brain damage. However, the role of PPAR?'s co-regulators during cerebral ischemia remains largely unknown. Here, we show that the transcription factor IRF6 is a novel PPAR? co-regulator that directly binds to and suppresses PPAR? activity in murine cerebrovascular endothelial cells. Moreover, IRF6 was also revealed to be a transcriptional target of PPAR? suppression, with PPAR? silencing significantly promoting IRF6 expression in cerebrovascular endothelial cells. In addition, IRF6 silencing significantly promoted pioglitazone's cytoprotective effects in ischemic murine cerebrovascular endothelial cells. Mechanistically, IRF6 significantly suppressed PPAR?'s transcriptional inhibition of the ischemia-induced, pro-apoptotic microRNA miR-106a. In conclusion, we identified IRF6 as a novel PPAR? co-suppressor that serves a key role in suppressing PPAR?-mediated cerebrovascular endothelial cytoprotection following ischemia. Further investigation into IRF6 and other PPAR? co-regulators should provide additional insights into PPAR?'s cytoprotective role in the cerebrovascular endothelium following stroke.

SUBMITTER: Huang R 

PROVIDER: S-EPMC5438409 | biostudies-literature | 2017 May

REPOSITORIES: biostudies-literature