Dabravolski Siarhei A, Popov Mikhail A, Utkina Aleksandra S, Babayeva Gulalek A, Maksaeva Anastasia O, Sukhorukov Vasily N, Orekhov Alexander N
Department of Biotechnology Engineering, Braude Academic College of Engineering, Snunit 51P.O. Box 78, 2161002, Karmiel, Israel.
Institute of General Pathology and Pathophysiology, 8 Baltiyskaya Street, Moscow, 125315, Russia.
Mol Cell Biochem. 2025 Apr 16. doi: 10.1007/s11010-025-05285-0.
Adipose-derived mesenchymal stem cells (AD-MSCs) are a promising therapeutic modality for cardiovascular diseases due to their immunomodulatory, anti-inflammatory, and pro-angiogenic properties. This manuscript explores the current status, challenges, and future directions of AD-MSC therapies, focusing on their application in atherosclerosis (AS), myocardial infarction (MI), and heart failure (HF). Preclinical studies highlight AD-MSC's ability to stabilise atherosclerotic plaques, reduce inflammation, and enhance myocardial repair through mechanisms such as macrophage polarisation, endothelial protection, and angiogenesis. Genetically and pharmacologically modified AD-MSCs, including those overexpressing SIRT1, IGF-1, and PD-L1 or primed with bioactive compounds, exhibit superior efficacy compared to unmodified cells. These modifications enhance cell survival, immunopotency, and reparative capacity, showcasing the potential for tailored therapies. However, clinical translation faces significant hurdles. While recent clinical trials have confirmed the safety of AD-MSC therapy, their efficacy remains inconsistent, necessitating further optimisation of patient selection, dosing strategies, and delivery methods. Donor variability, particularly in patients with co-morbidities like type 2 diabetes (T2D) or obesity, impairs AD-MSC efficacy. Emerging research on extracellular vesicles (EVs) derived from AD-MSC offers a promising cell-free alternative, retaining the therapeutic benefits while mitigating risks. Future perspectives emphasise the need for multidisciplinary approaches to overcome these limitations. Strategies include refining genetic modifications, exploring EV-based therapies, and integrating personalised medicine and advanced diagnostic tools. By addressing these challenges, AD-MSC therapies hold the potential to revolutionise the treatment of cardiovascular diseases, providing innovative solutions to improve patient outcomes.
脂肪来源的间充质干细胞(AD-MSCs)因其免疫调节、抗炎和促血管生成特性,是治疗心血管疾病的一种有前景的治疗方式。本手稿探讨了AD-MSC疗法的现状、挑战和未来方向,重点关注其在动脉粥样硬化(AS)、心肌梗死(MI)和心力衰竭(HF)中的应用。临床前研究强调了AD-MSC通过巨噬细胞极化、内皮保护和血管生成等机制稳定动脉粥样硬化斑块、减轻炎症和增强心肌修复的能力。基因和药物修饰的AD-MSCs,包括那些过表达SIRT1、IGF-1和PD-L1或用生物活性化合物预处理的细胞,与未修饰的细胞相比表现出更高的疗效。这些修饰增强了细胞存活、免疫能力和修复能力,展示了定制疗法的潜力。然而,临床转化面临重大障碍。虽然最近的临床试验证实了AD-MSC疗法的安全性,但其疗效仍然不一致,需要进一步优化患者选择、给药策略和递送方法。供体变异性,特别是在患有2型糖尿病(T2D)或肥胖等合并症的患者中,会损害AD-MSC的疗效。对源自AD-MSC的细胞外囊泡(EVs)的新兴研究提供了一种有前景的无细胞替代方案,在降低风险的同时保留了治疗益处。未来展望强调需要多学科方法来克服这些限制。策略包括完善基因修饰、探索基于EV的疗法,以及整合个性化医学和先进诊断工具。通过应对这些挑战,AD-MSC疗法有可能彻底改变心血管疾病的治疗方式,提供创新解决方案以改善患者预后。