Adult Stem Cells from the Hyaluronic Acid-Rich Node and Duct System Differentiate into Neuronal Cells and Repair Brain Injury

被引:32
作者
Lee, Seung J. [1 ,2 ]
Park, Sang H. [1 ,3 ]
Kim, Yu I. [1 ]
Hwang, Sunhee [1 ]
Kwon, Patrick M. [4 ]
Han, In S. [2 ]
Kwon, Byoung S. [1 ,5 ]
机构
[1] Natl Canc Ctr, Canc Immunol Branch, Ilsan, Gyeonggi, South Korea
[2] Univ Ulsan, Dept Biol Sci, Ulsan 680749, South Korea
[3] Sungkyunkwan Univ, Dept Biol Sci, Suwon, Gyeonggi, South Korea
[4] Icahn Sch Med Mt Sinai, Dept Neurol, New York, NY 10029 USA
[5] Tulane Univ, Dept Med, Hlth Sci Ctr, Clin Immunol Sect, New Orleans, LA 70118 USA
基金
新加坡国家研究基金会;
关键词
BONE-MARROW; PROGENITOR CELLS; ISCHEMIC BRAIN; NEURAL STEM; POPULATION; ORGANS; MICE; EXPRESSION; TISSUES; BLOOD;
D O I
10.1089/scd.2014.0142
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The existence of a hyaluronic acid-rich node and duct system (HAR-NDS) within the lymphatic and blood vessels was demonstrated previously. The HAR-NDS was enriched with small (3.0-5.0 mu m in diameter), adult stem cells with properties similar to those of the very small embryonic-like stem cells (VSELs). Sca-1(+)Lin(-)CD45(-) cells were enriched approximately 100-fold in the intravascular HAR-NDS compared with the bone marrow. We named these adult stem cells "node and duct stem cells (NDSCs)." NDSCs formed colonies on C2C12 feeder layers, were positive for fetal alkaline phosphatase, and could be subcultured on the feeder layers. NDSCs were Oct4(+)Nanog(+)SSEA-1(+)Sox2(+), while VSELs were Oct4(+)Nanog(+)SSEA-1(+)Sox2(-). NDSCs had higher sphere-forming efficiency and proliferative potential than VSELs, and they were found to differentiate into neuronal cells in vitro. Injection of NDSCs into mice partially repaired ischemic brain damage. Thus, we report the discovery of potential adult stem cells that may be involved in tissue regeneration. The intravascular HAR-NDS may serve as a route that delivers these stem cells to their target tissues.
引用
收藏
页码:2831 / 2840
页数:10
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