miR579-3p is an inhibitory modulator of neointimal hyperplasia and transcription factors c-MYB and KLF4.
Xiujie XieTakuro ShirasuJing LiLian-Wang GuoCraig K KentPublished in: Cell death discovery (2023)
Neointimal hyperplasia (IH) is a common vascular pathology that typically manifests in in-stent restenosis and bypass vein graft failure. Smooth muscle cell (SMC) phenotypic switching is central to IH, both regulated by some microRNAs, yet the role of miR579-3p, a scarcely studied microRNA, is not known. Unbiased bioinformatic analysis suggested that miR579-3p was repressed in human primary SMCs treated with different pro-IH cytokines. Moreover, miR579-3p was software-predicted to target both c-MYB and KLF4 - two master transcription factors known to promote SMC phenotypic switching. Interestingly, treating injured rat carotid arteries via local infusion of miR579-3p-expressing lentivirus reduced IH 14 days after injury. In cultured human SMCs, transfection with miR579-3p inhibited SMC phenotypic switching, as indicated by decreased proliferation/migration and increased SMC contractile proteins. miR579-3p transfection downregulated c-MYB and KLF4, and luciferase assays indicated miR579-3p's targeting of the 3'UTRs of the c-MYB and KLF4 mRNAs. In vivo, immunohistochemistry showed that treatment of injured rat arteries with the miR579-3p lentivirus reduced c-MYB and KLF4 and increased SMC contractile proteins. Thus, this study identifies miR579-3p as a previously unrecognized small-RNA inhibitor of IH and SMC phenotypic switch involving its targeting of c-MYB and KLF4. Further studies on miR579-3p may provide an opportunity for translation to develop IH-mitigating new therapeutics.
Keyphrases
- transcription factor
- smooth muscle
- endothelial cells
- dna binding
- genome wide identification
- skeletal muscle
- oxidative stress
- single cell
- induced pluripotent stem cells
- cancer therapy
- low dose
- pluripotent stem cells
- blood flow
- dna methylation
- cell therapy
- anti inflammatory
- bone marrow
- combination therapy
- data analysis
- replacement therapy
- cell fate