Transplantation of differentiated bone marrow stromal cells promotes motor functional recovery in rats with stroke

被引:46
作者
Huang, Wen [1 ]
Mo, Xuean [1 ]
Qin, Chao [1 ]
Zheng, Jinou [1 ]
Liang, Zhijian [1 ]
Zhang, Cheng [2 ]
机构
[1] Guangxi Med Univ, Dept Neurol, Affiliated Hosp 1, Nanning 530021, Peoples R China
[2] Sun Yat Sen Univ, Dept Neurol, Guangzhou 510275, Guangdong, Peoples R China
关键词
Bone marrow stromal cells; Brain-derived neurotrophic factor; Middle cerebral artery occlusion; Transplantation; NEURON-SPECIFIC ENOLASE; MIDDLE CEREBRAL-ARTERY; REDUCES INFARCT SIZE; NEUROTROPHIC FACTOR; BRAIN; OCCLUSION; ISCHEMIA; BLOOD; BDNF; PROLIFERATION;
D O I
10.1179/1743132812Y.0000000151
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To investigate the effects of transplantation into rats with stroke of bone marrow-derived mesenchymal stem cells (MSCs) induced by brain-derived neurotrophic factor (BDNF). Materials and methods: MSCs were harvested from 6-week-old Sprague-Dawley male rats, and transplanted into adult Sprague-Dawley male rats with transient middle cerebral artery occlusion. At 48 hours after stroke, the adult rats, weighing 250-280 g, were injected via the tail vein with 1 x 10(7) MSCs or MSCs induced by BDNF (BDNF-MSCs) suspended in 1 ml phosphate-buffered saline. All animals underwent the neurological function test for 14 days. Infarct volume and blood-brain barrier permeability assay were assessed on day 14 post-middle cerebral artery occlusion. Western blotting and immunohistochemical staining were used to detect the protein expression of neuron-specific enolase (NSE). Results: Both BDNF-MSCs and MSCs produced improvement in neurological deficits compared with vehicle controls on day 14 (P<0.05). In particular, the group transplanted with BDNF-MSCs exhibited significant recovery of motor function compared with the group transplanted with MSCs alone (P<0.05). Both BDNF-MSCs and MSCs, but particularly the former, reduced infarct volume, improved blood-brain barrier dysfunction, reduced serum NSE levels, activated the NSE activity, and inhibited neuronal apoptosis in the ischemic boundary zone. Conclusions: BDNF-MSCs might contribute to the motor function improvement partly by reducing neuronal damage via upregulating the NSE expression level and inhibiting neuronal apoptosis.
引用
收藏
页码:320 / 328
页数:9
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