Ricci Alessia, Cataldi Amelia, Gallorini Marialucia, di Giacomo Viviana, Rapino Monica, Di Pietro Natalia, Mantarro Marco, Piattelli Adriano, Zara Susi
Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, 66100 Chieti, Italy.
Ud'A Techlab, "G. d'Annunzio" University of Chieti-Pescara, 66100 Chieti, Italy.
Cells. 2025 Feb 24;14(5):332. doi: 10.3390/cells14050332.
The vascular system is primarily responsible for orchestrating the underlying healing processes to achieve tissue regeneration, thus the promotion of angiogenic events could be a useful strategy to repair injured tissues. Among several approaches to stimulate tissue regeneration, non-invasive devices are currently widely diffused. Complex Magnetic Fields (CMFs) are innovative pulsed multifrequency electromagnetic fields used for their promising results in clinical applications, such as diabetic foot treatment or edema resorption. Nevertheless, few papers are available demonstrating the biological mechanisms involved. In this paper, in order to understand CMFs' capability to promote angiogenic events, Regenerative Tissue Program (RTP) was applied to an in vitro Endothelial Cells (ECs) model. ECs were stimulated with (I) 2 RTP consecutive cycles, (II) with an interval of 8 h (T0 + T8), or (III) 24 h (T0 + T24) from one cycle to another. Results demonstrate that (I) extracellular matrix degradation is promoted through matrix metalloproteinases 2 and 9 modulation, leading to an increased cell migratory capability; (II) CMFs support EC growth, activating Integrin β1-Erk-Cdk2 pathway and sustaining G1/S transition; (III) vessel morphogenesis is promoted when CMFs are applied. In conclusion, the promising clinical results are supported by in vitro analyses which evidence that main angiogenic events are stimulated by CMFs.
血管系统主要负责协调潜在的愈合过程以实现组织再生,因此促进血管生成事件可能是修复受损组织的一种有效策略。在几种刺激组织再生的方法中,非侵入性设备目前广泛应用。复合磁场(CMFs)是一种创新的脉冲多频电磁场,因其在临床应用(如糖尿病足治疗或水肿吸收)中取得的良好效果而被使用。然而,很少有论文证明其中涉及的生物学机制。在本文中,为了了解CMFs促进血管生成事件的能力,将再生组织程序(RTP)应用于体外内皮细胞(ECs)模型。用(I)连续2个RTP周期、(II)周期之间间隔8小时(T0 + T8)或(III)周期之间间隔24小时(T0 + T24)刺激ECs。结果表明,(I)通过基质金属蛋白酶2和9的调节促进细胞外基质降解,导致细胞迁移能力增强;(II)CMFs支持EC生长,激活整合素β1-Erk-Cdk2通路并维持G1/S期转换;(III)应用CMFs时促进血管形态发生。总之,体外分析支持了CMFs刺激主要血管生成事件这一有前景的临床结果。