Abad-Contreras David E, Martínez-Ortiz Ana K, Martínez-López Valentín, Laparra-Escareño Hugo, Martínez-García Francisco Drusso, Pérez-Calixto Daniel, Vazquez-Victorio Genaro, Sepúlveda-Robles Omar, Rosas-Vargas Haydeé, Piña-Barba Cristina, Rodríguez-López Leonardo A, Giraldo-Gomez David M, Hinojosa Carlos A
Laboratory for Biomaterials, Materials Research Institute, National Autonomous University of Mexico (UNAM), Circuito Exterior, Ciudad Universitaria, Avenida Universidad 3000, Coyoacán, Ciudad de México 04510, Mexico.
Laboratory for Biomaterials, Materials Research Institute, National Autonomous University of Mexico (UNAM), Circuito Exterior, Ciudad Universitaria, Avenida Universidad 3000, Coyoacán, Ciudad de México 04510, Mexico; Faculty of Chemistry, National Autonomous University of Mexico (UNAM), Circuito Exterior, Ciudad Universitaria, Avenida Universidad 3000, Coyoacán, Ciudad de México 04510, Mexico.
Tissue Cell. 2025 Apr;93:102686. doi: 10.1016/j.tice.2024.102686. Epub 2024 Dec 19.
This work presents strong evidence supporting the use of decellularized human iliac arteries combined with adipose tissue-derived stem cells (hASCs) as a promising alternative for vascular tissue engineering, opening the path to future treatments for peripheral artery disease (PAD). PAD is a progressive condition with high rates of amputation and mortality due to ischemic damage and limited graft options. Traditional synthetic grafts often fail due to poor integration, while autologous grafts may be unsuitable for patients with compromised vascular health. This study explores the potential of decellularized human iliac arteries as scaffolds for vascular grafts, focusing on preserving extracellular matrix (ECM) ultrastructure while minimizing immunogenic response. A perfusion-based protocol with enzymatic and detergent agents effectively removed cellular material, resulting in scaffolds with preserved ECM architecture, including organized collagen and elastin fibers. To assess scaffold bioactivity, hASCs were seeded onto the decellularized ECM, demonstrating high viability. Structural assessments, including histological staining and mechanical testing, confirmed that decellularized arteries retained their hierarchical structure and exhibited increased stiffness, suggesting an adaptive realignment of ECM fibers. Thermal and ultrastructural analyses further showed that decellularized scaffolds maintained stability and integrity comparable to native tissue, underscoring their durability for clinical applications. The human iliac artery shows potential as a vascular scaffold due to its accessibility and the ability to support the viability of hASC. Future research will emphasize in vivo validation and strategies for functional recellularization to evaluate the clinical viability of these engineered vascular grafts.
这项工作提供了有力证据,支持使用脱细胞人髂动脉与脂肪组织衍生干细胞(hASC)相结合,作为血管组织工程的一种有前景的替代方案,为外周动脉疾病(PAD)的未来治疗开辟了道路。PAD是一种进行性疾病,由于缺血性损伤和有限的移植选择,截肢率和死亡率很高。传统的合成移植物往往因整合不良而失败,而自体移植物可能不适用于血管健康受损的患者。本研究探索了脱细胞人髂动脉作为血管移植物支架的潜力,重点是保留细胞外基质(ECM)超微结构,同时将免疫原性反应降至最低。一种基于灌注的方案结合酶和去污剂有效地去除了细胞物质,产生了保留ECM结构的支架,包括有组织的胶原纤维和弹性纤维。为了评估支架的生物活性,将hASC接种到脱细胞ECM上,显示出高存活率。包括组织学染色和力学测试在内的结构评估证实,脱细胞动脉保留了其分层结构,并表现出硬度增加,表明ECM纤维发生了适应性重新排列。热分析和超微结构分析进一步表明,脱细胞支架保持了与天然组织相当的稳定性和完整性,强调了它们在临床应用中的耐久性。人髂动脉因其可及性和支持hASC存活的能力而显示出作为血管支架的潜力。未来的研究将强调体内验证和功能再细胞化策略,以评估这些工程血管移植物的临床可行性。