Qin Kang, Wang Fei, Simpson Russell M L, Zheng Xueni, Wang He, Hu Yanhua, Gao Zhixian, Xu Qingbo, Zhao Qiang
State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences, Nankai University, Tianjin, 300071, China; Tianjin Key Laboratory of Risk Assessment and Control Technology for Environment and Food Safety, Tianjin Institute of Environment and Operational Medicine, Tianjin, 300050, China.
State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences, Nankai University, Tianjin, 300071, China.
Biomaterials. 2020 Oct;257:120226. doi: 10.1016/j.biomaterials.2020.120226. Epub 2020 Jul 16.
The regeneration of smooth muscle with physiological functions has been a key challenge in vascular tissue engineering. Hyaluronan (HA), as a major component of the extracellular matrix, plays a vital role in regulating tissue injury and repair. In this study, a biomimetic vascular graft was prepared by co-electrospinning of synthetic degradable polymers and native ECM components including collagen type-I as well as low and high molecular weight HA (LMW HA and HMW HA). Upon implantation in the rat abdominal aorta, the grafts exhibited sustained HA release that effectively enhanced the regeneration of vascular smooth muscle. Besides, LMW HA loaded vascular grafts demonstrated rapid endothelialization compared to the other groups. More importantly, HA-loaded poly(L-lactide-co-caprolactone) grafts demonstrated an optimal vascular media layer accompanied by well-organized elastin fibers after long-term implantation (6 months), and they maintained potent physiological function up to 1/3 that of the native artery. In contrast, inadequate smooth muscle regeneration was observed in poly(ε-caprolactone) grafts due to slow degradation restricting the regeneration. The mechanism was further investigated and explained by the HA-induced migration of smooth muscle cell (SMC) via CD44-mediated signaling. Besides, low molecular weight HA can promote the migration of vascular progenitor cells that further differentiate into SMCs. These results highlight the importance of HA in the regeneration of functional vascular smooth muscle, and provide a new insight into the fabrication of tissue engineering vascular grafts (TEVGs) via combining rapidly degradable polymers and bioactive ECM components that hold great translational potential.
具有生理功能的平滑肌再生一直是血管组织工程中的关键挑战。透明质酸(HA)作为细胞外基质的主要成分,在调节组织损伤和修复中起着至关重要的作用。在本研究中,通过将合成可降解聚合物与天然细胞外基质成分(包括I型胶原蛋白以及低分子量和高分子量HA(LMW HA和HMW HA))共电纺制备了一种仿生血管移植物。植入大鼠腹主动脉后,移植物表现出持续的HA释放,有效促进了血管平滑肌的再生。此外,与其他组相比,负载LMW HA的血管移植物表现出快速的内皮化。更重要的是,负载HA的聚(L-丙交酯-共-己内酯)移植物在长期植入(6个月)后表现出最佳的血管中层,并伴有组织良好的弹性纤维,并且它们保持了高达天然动脉1/3的强大生理功能。相比之下,聚(ε-己内酯)移植物中观察到平滑肌再生不足,因为降解缓慢限制了再生。通过HA诱导的平滑肌细胞(SMC)通过CD44介导的信号迁移进一步研究并解释了其机制。此外,低分子量HA可以促进血管祖细胞的迁移,这些祖细胞进一步分化为SMC。这些结果突出了HA在功能性血管平滑肌再生中的重要性,并为通过结合具有巨大转化潜力的快速可降解聚合物和生物活性细胞外基质成分来制造组织工程血管移植物(TEVG)提供了新的见解。