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Updated: Jan 20, 2026

Measuring Proliferation of Vascular Smooth Muscle Cells Using Click Chemistry
Published on: October 30, 2019
Inhibitory effects of herbal decoction Ojeoksan on proliferation and migration in vascular smooth muscle cells
Abstract:
The proliferation of vascular smooth muscle cells plays a crucial role in pathogenesis of cardiovascular disease. The principal objective of this study was to determine the effects of Ojeoksan (OJS) on human aortic smooth muscle cell (HASMC) proliferation induced by tumor necrosis factor α (TNF-aα). Thymidine incorporation after TNF-α treatment was increased and this effect was inhibited significantly by OJS treatment. HASMC proliferation and migration by kinetic live cell imaging were also reduced by treatment with OJS. TNF-α induced the expression of cyclins/cyclin-dependent kinases (CDKs) and reduced the expression of p21waf1/cip1/p27kip1. However, OJS also attenuated the expression of TNF-α-induced cell-cycle regulatory proteins. The results of Western blot analysis demonstrated that the TNF-α treated HASMC secreted gelatinases, probably including MMP-2/-9, which may be involved in the invasion and migration of HASMC. Additionally, OJS suppressed the mRNA expression levels of matrix metalloproteinase-2/-9 (MMP-2/-9) in a dose-dependent manner. OJS inhibited the production of TNF-α-induced hydrogen peroxide (H2O2) and the formation of DCF-sensitive intracellular reactive oxygen species (ROS). Further, OJS suppressed the nuclear translocation and phosphorylation of inhibitor of kappa B-α (IκB-α) of nuclear factor κB (NF-κB) under TNF-α conditions. Our results demonstrate that OJS exerts inhibitory effects on TNF-α-induced HASMC proliferation and migration, suggesting the involvement of the inhibition of both MMP-2 and MMP-9 expressions, and the downregulation of ROS/NF-κB signaling. Thus, herbal decoction OJS may be a possible therapeutic approach to the inhibition of cardiovascular disease including atherosclerosis.
Insights
Ojeoksan (OJS) significantly inhibits human aortic smooth muscle cell proliferation and migration induced by tumor necrosis factor-alpha (TNF-α). This herbal treatment downregulates reactive oxygen species (ROS) and nuclear factor-kappa B (NF-κB) signaling pathways, offering potential for cardiovascular disease therapy.
Area of Science:
- Cardiovascular Biology
- Pharmacology
- Cell Biology
Background:
- Vascular smooth muscle cell proliferation is a key factor in cardiovascular disease development.
- Tumor necrosis factor-alpha (TNF-α) is a pro-inflammatory cytokine that stimulates HASMC proliferation.
Purpose of the Study:
- To investigate the inhibitory effects of Ojeoksan (OJS) on TNF-α-induced human aortic smooth muscle cell (HASMC) proliferation and migration.
- To elucidate the underlying molecular mechanisms of OJS action.
Main Methods:
- Assessed thymidine incorporation and live cell imaging for HASMC proliferation and migration.
- Analyzed cell-cycle regulatory proteins (cyclins, CDKs, p21, p27) using Western blot.
- Quantified matrix metalloproteinase (MMP-2/-9) mRNA expression via RT-PCR.
- Measured hydrogen peroxide (H₂O₂) and reactive oxygen species (ROS) production.
- Investigated nuclear factor-kappa B (NF-κB) signaling pathway activation (IκB-α phosphorylation and translocation).
Main Results:
- OJS significantly inhibited TNF-α-induced thymidine incorporation, proliferation, and migration in HASMCs.
- OJS attenuated the expression of TNF-α-induced cyclins/CDKs and modulated p21/p27 levels.
- OJS suppressed TNF-α-induced mRNA expression of MMP-2/-9, ROS production, and NF-κB pathway activation.
- OJS inhibited the phosphorylation and nuclear translocation of IκB-α.
Conclusions:
- OJS demonstrates significant inhibitory effects on TNF-α-induced HASMC proliferation and migration.
- The mechanisms involve the downregulation of MMP-2/-9 expression and the ROS/NF-κB signaling pathway.
- OJS presents a potential therapeutic strategy for cardiovascular diseases like atherosclerosis.
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