Endothelial Gata5 transcription factor regulates blood pressure.
Smail MessaoudiYing HeAlex GutsolAndrew WightRichard L HébertRagnar O VilmundarsonAndrew P MakrigiannisJohn ChalmersPavel HametJohanne TremblayRuth McPhersonAlexandre F R StewartRhian M TouyzMona NemerPublished in: Nature communications (2015)
Despite its high prevalence and economic burden, the aetiology of human hypertension remains incompletely understood. Here we identify the transcription factor GATA5, as a new regulator of blood pressure (BP). GATA5 is expressed in microvascular endothelial cells and its genetic inactivation in mice (Gata5-null) leads to vascular endothelial dysfunction and hypertension. Endothelial-specific inactivation of Gata5 mimics the hypertensive phenotype of the Gata5-null mice, suggestive of an important role for GATA5 in endothelial homeostasis. Transcriptomic analysis of human microvascular endothelial cells with GATA5 knockdown reveals that GATA5 affects several genes and pathways critical for proper endothelial function, such as PKA and nitric oxide pathways. Consistent with a role in human hypertension, we report genetic association of variants at the GATA5 locus with hypertension traits in two large independent cohorts. Our results unveil an unsuspected link between GATA5 and a prominent human condition, and provide a new animal model for hypertension.
Keyphrases
- transcription factor
- endothelial cells
- blood pressure
- dna binding
- high glucose
- genome wide identification
- hypertensive patients
- nitric oxide
- heart rate
- genome wide
- vascular endothelial growth factor
- induced pluripotent stem cells
- type diabetes
- pluripotent stem cells
- copy number
- gene expression
- risk factors
- insulin resistance
- dna methylation
- hydrogen peroxide
- high fat diet induced
- weight loss