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在体共培养平滑肌细胞与内皮细胞促进组织工程血管快速血管化。

Rapid vascularization of tissue-engineered vascular grafts in vivo by endothelial cells in co-culture with smooth muscle cells.

机构信息

Department of Pediatric Thoracic and Cardiovascular Surgery, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

出版信息

J Mater Sci Mater Med. 2012 Apr;23(4):1109-17. doi: 10.1007/s10856-012-4576-8. Epub 2012 Feb 14.

Abstract

A major challenge facing the development of tissue-engineered vascular grafts (TEVGs), promising living replacements for diseased vascular structures, is enhancing angiogenesis. To promote rapid vascularization, endothelial cells (ECs) were co-cultured with smooth muscle cells (SMCs) in decellularized small intestinal submucosa scaffolds to regenerate angiogenic-TEVGs (A-TEVGs). Observation of the A-TEVGs at 1 month post-implantation revealed that a rich network of neocapillaries lining the blood vessel wall had developed; that the ECs of the neovasculatures had been derived from previously seeded ECs and later invading ECs of the host's vascular bed; that tissue vascularization had not significantly impaired mechanical properties; and that the maximal tensile strength of the A-TEVGs was of the same order of magnitude as that of native porcine femoral arteries. These results indicate that of the co-culturing of ECs with SMCs could enhance vascularization of TEVGs in vivo, possibly increasing graft perfusion and host integration.

摘要

组织工程血管移植物(TEVGs)的发展面临着一个主要挑战,即增强血管生成,以提供有希望的患病血管结构的活体替代品。为了促进快速血管化,将内皮细胞(ECs)与平滑肌细胞(SMCs)共培养在脱细胞的小肠黏膜下层支架中,以再生血管生成 TEVGs(A-TEVGs)。在植入后 1 个月观察 A-TEVGs 时发现,血管壁上已经形成了丰富的新毛细血管网络;新生血管的 ECs 来源于先前接种的 ECs 和后来入侵宿主血管床的 ECs;组织血管化并没有显著损害机械性能;A-TEVGs 的最大拉伸强度与天然猪股动脉处于同一数量级。这些结果表明,ECs 与 SMCs 的共培养可以增强体内 TEVGs 的血管生成,可能增加移植物灌注和宿主整合。

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