کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6263504 1613907 2013 13 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Genetically engineered bone marrow mesenchymal stem cells improve functional outcome in a rat model of epilepsy
ترجمه فارسی عنوان
سلول های بنیادی مزانشیمی مغز استخوان تولید شده توسط ژنتیک باعث بهبود عملکرد در مدل موش های صرعی می شود
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
چکیده انگلیسی


• Hes1 silencing can initiate GABAergic differentiation of BMSCs.
• GABAergic differentiation of Hesl silencing BMSCs contributes to the functional improvement.
• Genetically engineered BMSCs may be new strategy for the treatment of epilepsy.

Bone marrow mesenchymal stem cells (BMSCs) hold a great promising approach for the treatment of epilepsy owing to their distinctive characteristics and multi-potency. However, there is little research focusing on the multi-potency of BMSCs in the treatment of epilepsy, the present study was designed to examine the influence of genetically engineered BMSCs (GE-BMSCs) on the functional outcome in a rat model of epilepsy. First, Hes1 gene of BMSCs was genetically engineered by RNA interference (RNAi), and then the GABAergic differentiation of GE-BMSCs was tested in vitro. Second, the lithium chloride–pilocarpine induced epileptic rats were administrated with the GE-BMSCs, the behavioral observation and electroencephalography (EEG) monitoring was employed to analyze the functional outcome on the epileptic model at different time points (day 7, day 14, day 21 and day 28), followed by histological verification. In vitro test showed that Hes1 silencing could promote BMSCs to differentiate into GABAergic neuron-like cells. In vivo test showed that GE-BMSCs graft could further improve the functional recovery of the epileptic rats, and the GABAergic differentiation of grafted GE-BMSCs was correlated with the functional recovery. Taken together, these data suggest that GE-BMSCs can improve the functional outcome in a rat model of epilepsy.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research - Volume 1532, 26 September 2013, Pages 1–13