Therapeutic Potential of a Combination of Electroacupuncture and TrkB-Expressing Mesenchymal Stem Cells for Ischemic Stroke

被引:32
作者
Ahn, Sung Min [1 ]
Kim, Yu Ri [1 ,2 ]
Shin, Yong-Il [3 ]
Ha, Ki Tae [1 ,2 ,4 ]
Lee, Seo-Yeon [1 ,4 ]
Shin, Hwa Kyoung [1 ,2 ,4 ]
Choi, Byung Tae [1 ,2 ,4 ]
机构
[1] Pusan Natl Univ, Korean Med Sci Res Ctr Hlth Aging, Yangsan 50612, South Korea
[2] Pusan Natl Univ, Dept Korean Med Sci, Sch Korean Med, Yangsan 50612, South Korea
[3] Pusan Natl Univ, Sch Med, Dept Rehabil Med, Yangsan 50612, South Korea
[4] Pusan Natl Univ, Grad Training Program Korean Med Hlth Aging, Yangsan 50612, South Korea
基金
新加坡国家研究基金会;
关键词
Brain-derived neurotrophic factor; Electroacupuncture; Ischemic stroke; Mesenchymal stem cells; Neurotrophin-4; Tropomyosin receptor kinase B; MARROW STROMAL CELLS; CEREBRAL-ARTERY OCCLUSION; BONE-MARROW; NEUROTROPHIC FACTORS; FUNCTIONAL RECOVERY; NT4; GENE; BRAIN; NEUROGENESIS; PROLIFERATION; MECHANISMS;
D O I
10.1007/s12035-018-1067-z
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We prepared and grafted tropomyosin receptor kinase B (TrkB) gene-transfected mesenchymal stem cells (TrkB-MSCs) into the ischemic penumbra and investigated whether electroacupuncture (EA) treatment could promote functional recovery from ischemic stroke. For the behavioral test, TrkB-MSCs+EA resulted in significantly improved motor function compared to that obtained with MSCs+EA or TrkB-MSCs alone. At 30days after middle cerebral artery occlusion (MCAO), the largest number of grafted MSCs was detected in the TrkB-MSC+EA group. Some differentiation into immature neuroblasts and astrocytes was detected; however, only a few mature neuron-like cells were found. Compared to other treatments, TrkB-MSCs+EA upregulated the expression of mature brain-derived neurotrophic factor (BDNF) and neurotrophin-4/5 (NT4) and induced the activation of TrkB receptor and its transcription factor cAMP response element-binding protein (CREB). At 60days after MCAO, EA highly promoted the differentiation of TrkB-MSCs into mature neuron-like cells compared to the effect in MSCs. A selective TrkB antagonist, ANA-12, reverted the effect of TrkB-MSCs+EA in motor function recovery and survival of grafted MSCs. Our results suggest that EA combined with grafted TrkB-MSCs promotes the expression of BDNF and NT4, induces the differentiation of TrkB-MSCs, and improves motor function. TrkB-MSCs could serve as effective therapeutic agents for ischemic stroke if used in combination with BDNF/NT4-inducing therapeutic approaches.
引用
收藏
页码:157 / 173
页数:17
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