Combined treatment of vascular endothelial growth factor and human neural stem cells in experimental focal cerebral ischemia

被引:79
作者
Chu, K
Park, KI
Lee, ST
Jung, KH
Ko, SY
Kang, L
Sinn, DI
Lee, YS
Kim, SU
Kim, M
Roh, JK
机构
[1] Seoul Natl Univ Hosp, Dept Neurol, Clin Res Inst, Stroke & Neural Stem Cell Lab, Seoul 110744, South Korea
[2] Seoul Natl Univ, SNUMRC, Neurosci Res Inst, Program Neurosci, Seoul, South Korea
[3] Seoul Natl Univ Hosp, Ctr Alcohol & Drug Addict Res, Seoul 110744, South Korea
[4] Korea Ctr Dis Control & Prevent, Dept Dis Invest & Surveillance, Seoul, South Korea
[5] Seoul Municipal Boramae Hosp, Dept Neurol, Seoul, South Korea
[6] Ajou Univ, Brain Dis Res Ctr, Suwon 441749, South Korea
[7] Univ British Columbia, Univ British Columbia Hosp, Dept Med, Div Neurol, Vancouver, BC V5Z 1M9, Canada
关键词
neural stem cell; focal ischemia; recovery; transplantation; VEGF;
D O I
10.1016/j.neures.2005.08.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent studies have indicated the beneficial effects of vascular endothelial growth factor (VEGF), and transplanted neural stem cells (NSCs) in cerebral ischemia. We investigated the effects of the combined administration of NSCs and VEGF on focal cerebral ischemia in adult rats. Four groups (n = 12, respectively) - group 1 (ischemia-only), group 2 (ischemia + VEGF), group 3 (ischemia + NSCs) and group 4 (ischemia + NSCs + VEGF) - were compared. Human NSCs (HB 1.F3), labeled with Lac Z(+) or PKH26, were given intravenously 24 h after surgery (5 x 106 cells). At 48 h after surgery, recombinant human VEGF (50 mu g/kg) was infused intravenously (1 mu g/(kg min)). Behavioral tests using the modified limb placing and rotarod tests were performed every week following ischemia. Immunohistochemistry for endothelial barrier antigen (EBA), VEGF and Nissl staining were performed at day 35 after ischemia. Group 4 showed better behavioral recovery at 7, 14 and 28 days than group 3 (p = 0.020, 0.005 and 0.043, respectively). These functional recoveries were correlated with enhanced EBA immunoreactivities at day 35 after ischemia, especially in the ipsilesional striatum. Group 4 showed lesser degree of brain atrophy in cortex and striatum, when compared with other groups. The distribution of VEGF was not co-localized with NSCs. Our results suggest that VEGF may act synergistically on NSC-transplanted, ischemic brain via a pro-angiogenic effect. (c) 2005 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:384 / 390
页数:7
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