Enhancing neuronal growth from human endometrial stem cells derived neuron-like cells in three-dimensional fibrin gel for nerve tissue engineering

被引:44
|
作者
Navaei-Nigjeh, Mona [1 ,2 ]
Amoabedini, Ghasem [1 ,3 ,4 ]
Noroozi, Abbas [5 ]
Azami, Mahmoud [2 ]
Asmani, Mohammad N. [1 ]
Ebrahimi-Barough, Somayeh [2 ,5 ]
Saberi, Hooshang [5 ]
Ai, Armin [6 ]
Ai, Jafar [2 ,5 ]
机构
[1] Univ Tehran, Fac New Sci & Technol, Tehran, Iran
[2] Univ Tehran Med Sci, Sch Adv Technol Med, Dept Tissue Engn, Tehran, Iran
[3] Univ Tehran, Sch Engn, Dept Chem Engn, Tehran, Iran
[4] Univ Tehran, Res Ctr New Technol Life Sci Engn, Tehran, Iran
[5] Univ Tehran Med Sci, Brain & Spinal Injury Res Ctr, Tehran, Iran
[6] Univ Tehran Med Sci, Fac Dent, Tehran, Iran
关键词
neuronal growth; human endometrial stem cell; fibrin gel; nerve tissue engineering; CULTURE; SCAFFOLDS; DIFFERENTIATION; THROMBIN; SURVIVAL; DESIGN; SYSTEM;
D O I
10.1002/jbm.a.34921
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Nerve tissue engineering (NTE) is one of the most promising methods to restore central nerve systems in human health care. Three-dimensional (3D) distribution and growth of cells within the porous scaffold composed of nano-fibers are of clinical significance for NTE. In this study, an attempt was made to develop and characterize the use of fibrin gel and human endometrial stem cells (hEnSCs)-derived neuron-like cells simultaneously to support cell behavior especially neuron outgrowth. The structural and mechanical characteristics of fibrin gel scaffold were examined with SEM and rheometer. Also, hEnSCs-derived neuron-like cells were cultured in fibrin gel and were subsequently analyzed with immunofluorescent staining against neuronal markers. In parallel, the survival and growth rates of the cells were determined by MTT assay and neurite extension. At the end, cell-matrix interactions were investigated with SEM and TEM micrographs. Mechanical properties of fabricated scaf-fold were studied and results indicated appropriate choice of material, SEM and TEM showed excellent integration of cells with nanofibers regarding the relation between cells and fibrin gel. Immunofluorescent staining of fibrin gel after 6 days of cell seeding and culture demonstrated well expanded and incorporated network of neurons. In addition, viability, proliferation, and neuronal growth of seeded cells were analyzed at days 1, 3, and 6. Comparing those results with 2D culture of seeded cells showed positive effect of 3D culture. Taken together, the results suggest that fibrin can provide a suitable, three-dimensional scaffold for neuronal survival and outgrowth for regeneration of the central nervous system. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:2533 / 2543
页数:11
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