Porous nanofibrous PLLA scaffolds for vascular tissue engineering

被引:155
作者
Hu, Jiang [1 ]
Sun, Xuan [2 ,5 ,6 ]
Ma, Haiyun [1 ]
Xie, Changqing [2 ]
Chen, Y. Eugene [2 ]
Ma, Peter X. [1 ,3 ,4 ]
机构
[1] Univ Michigan, Dept Biol & Mat Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Ctr Cardiovasc, Med Ctr, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Ctr Macromol Sci & Engn, Ann Arbor, MI 48109 USA
[5] Cent S Univ, Inst Reprod & Stem Cell Engn, Changsha 410078, Hunan, Peoples R China
[6] Res Ctr Human Stem Cell, Changsha 410078, Hunan, Peoples R China
基金
美国国家卫生研究院;
关键词
Human aortic smooth muscle cells; Nanofibrous matrix; Porous scaffold; Differentiation; Vascular graft; MESENCHYMAL STEM-CELLS; SMOOTH-MUSCLE-CELLS; BLOOD-VESSEL; GROWTH-FACTOR; IN-VITRO; COLLAGEN; GRAFTS;
D O I
10.1016/j.biomaterials.2010.07.028
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Tissue-engineered small-diameter vascular grafts are needed for patients requiring replacement of their injured coronary and below-the-knee vessels. Understanding the interactions between the scaffolds and implanted cells and therefore the phenotype control of smooth muscle cells (SMCs) is critical for constructing functional vascular grafts. In this study, the effect of nanofibrous (NF) poly-L-lactide (PLLA) scaffolds on phenotype control of human aortic smooth muscle cells (HASMCs) was investigated. A tubular NF PLLA scaffold for blood vessel regeneration was fabricated and cell seeding studies showed cell distribution throughout the scaffold. It was found that NE PLLA scaffolds preferentially supported contractile phenotype of HASMCs under the in vitro culture conditions, as evidenced by elevated gene expression level of SMCs contractile markers including smooth muscle myosin heavy chain, smoothelin and myocardin. In vivo subcutaneous implantation studies confirmed HASMCs differentiation in the implants. Taken together, the results showed promising application of the porous NF PLLA scaffolds for reconstruction of tissue-engineered vascular grafts. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7971 / 7977
页数:7
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