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Enhancing trophic support of mesenchymal stem cells by ex vivo treatment with trophic factors

Authors
 Yun Jung Choi  ;  Wen Yu Li  ;  Gyeong Joon Moon  ;  Phil Hyu Lee  ;  Young Hwan Ahn  ;  Gwang Lee  ;  Oh Young Ban 
Citation
 JOURNAL OF THE NEUROLOGICAL SCIENCES, Vol.298(1-2) : 28-34, 2010 
Journal Title
JOURNAL OF THE NEUROLOGICAL SCIENCES
ISSN
 0022-510X 
Issue Date
2010
MeSH
Animals ; Brain Ischemia/complications ; Brain Ischemia/therapy* ; Brain-Derived Neurotrophic Factor/therapeutic use ; Cell Separation ; Cell Survival ; Cells, Cultured ; Dose-Response Relationship, Drug ; Enzyme-Linked Immunosorbent Assay ; Hepatocyte Growth Factor/therapeutic use ; Humans ; Intercellular Signaling Peptides and Proteins/administration & dosage ; Intercellular Signaling Peptides and Proteins/therapeutic use* ; Male ; Mesenchymal Stem Cell Transplantation/methods* ; Rats ; Rats, Sprague-Dawley ; Rats, Wistar ; Stroke/etiology ; Stroke/therapy* ; Vascular Endothelial Growth Factor A/therapeutic use
Keywords
Stroke, ischemic ; Stem cells ; Mesenchymal stem cells ; Bone marrow ; Trophic factors
Abstract
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.
Full Text
http://www.sciencedirect.com/science/article/pii/S0022510X10004399
DOI
10.1016/j.jns.2010.09.003
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
Yonsei Authors
Lee, Phil Hyu(이필휴) ORCID logo https://orcid.org/0000-0001-9931-8462
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/102744
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