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Published on: May 31, 2016
miR‑214 mediates vascular inflammation and apoptosis via PTEN expression
Mingliang Wang1, Min Liu1, Ting Ni1
1Department of Cardiology, Shanghai Putuo District People's Hospital, Shanghai 200060, P.R. China.
Abstract:
The present study aimed to investigate the role of miR‑214 on inflammation and apoptosis in the vascular system and to examine its potential mechanisms. Anti‑miR‑214 mimics were used to downregulate miR‑214 expression in HUVECs. Cell viability and the apoptosis rate were measured using MTT assay and flow cytometry. Tumor necrosis factor (TNF)‑α, interleukin (IL)‑1β, IL‑6 and IL‑18 levels were measured using ELISA kits. Following this, caspase‑3/9, Bax, phosphatase and tensin homolog (PTEN), nuclear factor (NF)‑κB and phosphorylated‑(p)‑protein kinase B (Akt) protein expression were analyzed using western blotting. The results demonstrated that anti‑miR‑214 mimics inhibited cell proliferation, increased apoptosis and inflammatory factors (TNF‑α, IL‑1β, IL‑6 and IL‑18 levels), inhibited cell proliferation, and induced Bax protein expression in TNF‑α‑induced vascular endothelial cells through induction of PTEN and NF‑κB protein expression and inhibition of Akt protein expression. The PTEN inhibitor inhibited the function of anti‑miR‑214 on apoptosis and inflammation in TNF‑α‑induced inflammation vascular endothelial cells through the PTEN/Akt signaling pathway. These results suggest that miR‑214 mediates vascular inflammation and apoptosis via PTEN expression.
Insights
MicroRNA-214 (miR-214) plays a key role in vascular inflammation and apoptosis. Downregulating miR-214 exacerbates these conditions by affecting the PTEN/Akt pathway.
Area of Science:
- Vascular Biology
- Molecular Biology
- Inflammation Research
Background:
- MicroRNAs (miRNAs) are crucial regulators of cellular processes.
- Vascular inflammation and apoptosis are key contributors to cardiovascular diseases.
- The specific role of miR-214 in vascular responses requires further elucidation.
Purpose of the Study:
- To investigate the function of miR-214 in vascular inflammation and apoptosis.
- To explore the underlying molecular mechanisms of miR-214's action.
- To determine the involvement of the PTEN/Akt signaling pathway.
Main Methods:
- Human Umbilical Vein Endothelial Cells (HUVECs) were treated with anti-miR-214 mimics.
- Cell viability and apoptosis were assessed using MTT assay and flow cytometry.
- Inflammatory cytokine levels (TNF-α, IL-1β, IL-6, IL-18) and protein expression (caspase-3/9, Bax, PTEN, NF-κB, p-Akt) were analyzed via ELISA and Western blotting.
Main Results:
- Downregulation of miR-214 increased apoptosis and inflammatory cytokine levels in TNF-α-induced HUVECs.
- Anti-miR-214 treatment elevated Bax, PTEN, and NF-κB expression while decreasing p-Akt.
- Inhibition of PTEN reversed the pro-apoptotic and pro-inflammatory effects of anti-miR-214.
Conclusions:
- miR-214 mediates vascular inflammation and apoptosis.
- The mechanism involves the regulation of PTEN expression and the PTEN/Akt signaling pathway.
- Targeting miR-214 could be a potential therapeutic strategy for vascular diseases.
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