Mousso Thomas, Rice Kalina, Tumenbayar Bat-Ider, Pham Khanh, Heo Yuna, Heo Su Chin, Lee Kwonmoo, Lombardo Andrew T, Bae Yongho
Department of Pathology and Anatomical Sciences, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York 14203, USA.
Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York 14203, USA.
APL Bioeng. 2025 Jun 4;9(2):026120. doi: 10.1063/5.0252766. eCollection 2025 Jun.
Arterial stiffness is a contributor to cardiovascular diseases (CVDs) and is associated with the aberrant migration of vascular smooth muscle cells (VSMCs). However, the mechanisms driving VSMC migration in stiff environments remain unclear. We recently demonstrated that survivin is upregulated in mouse and human VSMCs cultured on stiff hydrogels, where it modulates stiffness-mediated cell proliferation. However, its role in stiffness-dependent VSMC migration remains unknown. To assess its impact on migration, we performed time-lapse microscopy on VSMCs seeded on fibronectin-coated soft and stiff hydrogels, mimicking the physiological stiffness of normal and diseased arteries. We observed that VSMC motility increased under stiff conditions, while pharmacologic or siRNA-mediated inhibition of survivin reduced stiffness-stimulated migration to rates similar to those observed under soft conditions. Further investigation revealed that cells on stiff hydrogels exhibited greater directional movement and robust lamellipodial protrusion compared to those on soft hydrogels. Interestingly, survivin-inhibited cells on stiff hydrogels showed reduced directional persistence and lamellipodial protrusion. We also found that survivin overexpression modestly increased cell motility and partially rescued the lack of directional persistence compared to green fluorescent protein (GFP)-expressing VSMCs on soft hydrogels. Mechanistically, stiffness- and survivin-dependent cell migration involves focal adhesion kinase (FAK) and actin dynamics, as stiffness increases phosphorylated FAK recruitment to focal adhesions and promotes actin organization and stress fiber formation-effects that are disrupted by survivin inhibition. In conclusion, our findings establish that mechanotransduction through a survivin-FAK-actin cascade converts extracellular matrix stiffness into stiffness-sensitive motility, suggesting that targeting this pathway may offer therapeutic strategies for CVD.
动脉僵硬度是心血管疾病(CVD)的一个促成因素,并且与血管平滑肌细胞(VSMC)的异常迁移有关。然而,在僵硬环境中驱动VSMC迁移的机制仍不清楚。我们最近证明,在僵硬水凝胶上培养的小鼠和人类VSMC中,生存素上调,在那里它调节硬度介导的细胞增殖。然而,其在硬度依赖性VSMC迁移中的作用仍然未知。为了评估其对迁移的影响,我们对接种在纤连蛋白包被的软质和硬质水凝胶上的VSMC进行了延时显微镜观察,模拟正常和患病动脉的生理硬度。我们观察到,在僵硬条件下VSMC的运动性增加,而药物或siRNA介导的生存素抑制将硬度刺激的迁移降低到与在软质条件下观察到的速率相似。进一步的研究表明,与软质水凝胶上的细胞相比,硬质水凝胶上的细胞表现出更大的定向运动和强大的片状伪足突出。有趣的是,硬质水凝胶上生存素抑制的细胞显示出定向持久性和片状伪足突出减少。我们还发现,与软质水凝胶上表达绿色荧光蛋白(GFP)的VSMC相比,生存素过表达适度增加了细胞运动性,并部分挽救了定向持久性的缺乏。从机制上讲,硬度和生存素依赖性细胞迁移涉及粘着斑激酶(FAK)和肌动蛋白动力学,因为硬度增加了磷酸化FAK募集到粘着斑,并促进肌动蛋白组织和应力纤维形成,而这些效应被生存素抑制所破坏。总之,我们的研究结果表明,通过生存素-FAK-肌动蛋白级联的机械转导将细胞外基质硬度转化为硬度敏感的运动性,这表明靶向该途径可能为CVD提供治疗策略。