间充质干细胞
碱性成纤维细胞生长因子
祖细胞
间质细胞
神经干细胞
移植
新生血管
骨髓
干细胞
细胞生物学
血管生成
化学
生物医学工程
免疫学
病理
医学
生长因子
癌症研究
生物
外科
内科学
受体
作者
Dai Matsuse,Masaaki Kitada,Fumitaka Ogura,Shohei Wakao,Misaki Kohama,Jun‐ichi Kira,Yasuhiko Tabata,Mari Dezawa
出处
期刊:Tissue Engineering Part A
[Mary Ann Liebert, Inc.]
日期:2011-04-02
卷期号:17 (15-16): 1993-2004
被引量:44
标识
DOI:10.1089/ten.tea.2010.0585
摘要
Bone marrow stromal cells (MSCs) are a useful source of cells because of their abundant supply and few associated ethical problems. We have previously reported that neural progenitor cells (NS-MSCs) can be effectively induced from MSCs and differentiate into neurons to contribute to functional recovery when transplanted into the rat stroke model. In this study, we attempted to enhance the therapeutic effects of NS-MSCs with a collagen sponge and basic fibroblast growth factor (bFGF) releasing microspheres. NS-MSCs were generated from MSCs by transfection of Notch-1 intracellular domain followed by culturing the cells in a free-floating culture system. The resulting NS-MSCs were transplanted into the rats with induced brain ischemia by using collagen sponges as scaffolds for transplanted cells, and with bFGF incorporated into gelatin microspheres to aid neovascularization around the transplanted region and proliferation of neural stem cells/neural progenitor cells. In culture, NS-MSCs successfully formed spheres containing cells highly expressing neural progenitor markers. Cell survival, neovascularization, and proliferation of host neural stem cells/neural progenitor cells were improved in animals that received NS-MSCs together with these biomaterials. Behavioral analysis also revealed significant functional recovery. These observations demonstrate that transplantation of NS-MSCs in combination with a collagen sponge and bFGF releasing microspheres significantly improves histological and functional recovery in the rat stroke model. When used with these biomaterials, NS-MSCs would be a promising cell source for treating stroke and neurodegenerative diseases.
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