The BET Protein Inhibitor Apabetalone Rescues Diabetes-Induced Impairment of Angiogenic Response by Epigenetic Regulation of Thrombospondin-1.
Shafeeq A MohammedMattia AlbieroSamuele AmbrosiniEra GoricaGergely KarsaiCarlo M CaravaggiStefano MasiGiovanni G CamiciFlorian A WenzlVincenzo CalderonePaolo MadedduSebastiano SciarrettaChristian M MatterGaia SpinettiThomas F LüscherFrank RuschitzkaSarah CostantinoGian Poalo FadiniFrancesco PaneniPublished in: Antioxidants & redox signaling (2022)
Aims: Therapeutic modulation of blood vessel growth holds promise for the prevention of limb ischemia in diabetic (DM) patients with peripheral artery disease (PAD). Epigenetic changes, namely, posttranslational histone modifications, participate in angiogenic response suggesting that chromatin-modifying drugs could be beneficial in this setting. Apabetalone (APA), a selective inhibitor of bromodomain (BRD) and bromodomain and extraterminal containing protein family (BET) proteins, prevents bromodomain-containing protein 4 (BRD4) interactions with chromatin thus modulating transcriptional programs in different organs. We sought to investigate whether APA affects angiogenic response in diabetes. Results: Compared with vehicle, APA restored tube formation and migration in human aortic endothelial cells (HAECs) exposed to high-glucose (HG) levels. Expression profiling of angiogenesis genes showed that APA prevents HG-induced upregulation of the antiangiogenic molecule thrombospondin-1 (THBS1). ChIP-seq and chromatin immunoprecipitation (ChIP) assays in HG-treated HAECs showed the enrichment of both BRD4 and active marks (H3K27ac) on THBS1 promoter, whereas BRD4 inhibition by APA prevented chromatin accessibility and THBS1 transcription. Mechanistically, we show that THBS1 inhibits angiogenesis by suppressing vascular endothelial growth factor A (VEGFA) signaling, while APA prevents these detrimental changes. In diabetic mice with hind limb ischemia, epigenetic editing by APA restored the THBS1/VEGFA axis, thus improving limb vascularization and perfusion, compared with vehicle-treated animals. Finally, epigenetic regulation of THBS1 by BRD4/H3K27ac was also reported in DM patients with PAD compared with nondiabetic controls. Innovation: This is the first study showing that BET protein inhibition by APA restores angiogenic response in experimental diabetes. Conclusions: Our findings set the stage for preclinical studies and exploratory clinical trials testing APA in diabetic PAD. Antioxid. Redox Signal. 36, 667-684.
Keyphrases
- endothelial cells
- high glucose
- vascular endothelial growth factor
- gene expression
- genome wide
- transcription factor
- dna methylation
- type diabetes
- glycemic control
- dna damage
- clinical trial
- cardiovascular disease
- protein protein
- amino acid
- high throughput
- peripheral artery disease
- mouse model
- public health
- circulating tumor cells
- heart failure
- crispr cas
- wound healing
- randomized controlled trial
- binding protein
- signaling pathway
- rna seq
- single cell
- stem cells
- oxidative stress
- aortic valve
- fluorescent probe
- atrial fibrillation
- diabetic rats
- insulin resistance
- mesenchymal stem cells
- cell therapy
- left ventricular
- long non coding rna
- heat shock
- stress induced
- small molecule