共 36 条
Enhancing trophic support of mesenchymal stem cells by ex vivo treatment with trophic factors
被引:32
作者:
Choi, Yun Jung
[2
]
Li, Wen Yu
[3
]
Moon, Gyeong Joon
Lee, Phil Hyu
[4
]
Ahn, Young Hwan
[5
]
Lee, Gwang
[2
]
Bang, Oh Young
[1
]
机构:
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Neurol,Neurosci Ctr, Seoul 135710, South Korea
[2] Ajou Univ, Sch Med, Brain Dis Res Ctr, Suwon 441749, South Korea
[3] Sir Run Run Shaw Hosp, Dept Neurol, Hangzhou, Zhejiang, Peoples R China
[4] Yonsei Univ, Sch Med, Dept Neurol, Seoul 120749, South Korea
[5] Ajou Univ, Sch Med, Dept Neurosurg, Suwon 441749, South Korea
基金:
新加坡国家研究基金会;
关键词:
Stroke;
ischemic;
Stem cells;
Mesenchymal stem cells;
Bone marrow;
Trophic factors;
MARROW STROMAL CELLS;
CEREBRAL-ARTERY OCCLUSION;
GROWTH-FACTOR PRODUCTION;
NEUROTROPHIC FACTOR;
NERVOUS-SYSTEM;
ISCHEMIA MODEL;
ADULT-RAT;
BRAIN;
STROKE;
TRANSPLANTATION;
D O I:
10.1016/j.jns.2010.09.003
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Background: Several studies have examined the enhanced efficacy of mesenchymal stem cells (MSCs) using neurotrophic factor transfection in ischemic rat models. However, gene therapy, e.g., the application of MSCs transfected with neurotrophic factors, is not feasible in clinical practice for ethical reasons. Therefore, we evaluated cultivation with specific trophic factors in an attempt to enhance the efficacy of human MSCs (hMSCs) in ischemic stroke. Methods: Using quantitative sandwich enzyme-linked immunosorbent assay (ELISA), we analyzed the levels of trophic factors released from hMSCs after treatment with ischemic brain extract. Trophic factors were pretreated under ex vivo culture conditions. The concentrations of each trophic factor produced by the trophic factor-pretreated and non-pretreated hMSCs were then measured and compared. Results: hMSCs cultured with ischemic rat brain extract showed increased production of BDNF (brain-derived neurotrophic factor), VEGF (vascular endothelial growth factor) and HGF (hepatocyte growth factor). Ex vivo treatment with trophic factors led to a further increase in the production of the trophic factor by hMSC, suggesting autocrine regulation of hMSCs. The morphology and expression of surface markers of hMSCs were not changed, but the cell viability and cell proliferation ability increased after treatment with trophic factors. Conclusions: Our data indicate that hMSCs provide trophic support to the ischemic brain, which can be enhanced by ex vivo treatment of trophic factors during cultivation of hMSCs. (C) 2010 Elsevier B.V. All rights reserved.
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页码:28 / 34
页数:7
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