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MiR-124 regulates neural stem cells in the treatment of spinal cord injury

机译:MiR-124调节神经干细胞治疗脊髓损伤

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Several studies demonstrated that the overexpression of miR-124 in neural stem cells (NSCs) could lead the NSCs to differentiate into neurons and astrocytes, which may be important for functional recovery in spinal cord injury. The present study attempted to explore the potential repairing effect of the NSCs transfected with miR-124 for the rats with spinal cord injury (SCI). NSCs transfected with miR-124 were transplanted into rats by intravenous injection after SCI. The effects of miR-124 on the differentiation of NSCs and the treatment for the SCI-model rats were experimentally investigated. The reduction of cavity volume in focal lesions and Basso-Beattie-Bresnahan (BBB) scores were used as the criteria of functional recovery of the SCI-model rats. Up-regulation of miR-124 promoted the differentiation of NSCs. Transfection of miR-124 in NSCs dramatically increased the percentage of NeuN-positive cells, and reduced the percentage of GFAP-positive cells in vitro and in vivo respectively. All of the rats treated with NSCs transfected with miR-124 achieved the better functional recovery than the ones in NSCs and sham control groups. Furthermore, the systemic delivery of the NSCs transfected with miR-124 resulted in a reduction of lesion cavity volume of SCI-model rats. Thus, Overexpression of miR-124 can promote the differentiation of NSCs and play an important role in the repair of SCI. The utility of intravenous delivery of stem cells regulated with miR-124 to target lesion areas as a prospective therapeutic approach in acute spinal cord injury is very promising in the future.
机译:多项研究表明,miR-124在神经干细胞(NSC)中的过表达可能导致NSC分化为神经元和星形胶质细胞,这可能对脊髓损伤中的功能恢复很重要。本研究试图探讨用miR-124转染的NSC对脊髓损伤(SCI)大鼠的潜在修复作用。 SCI后通过静脉注射将用miR-124转染的NSC移植到大鼠中。实验研究了miR-124对NSCs分化的影响以及对SCI模型大鼠的治疗。局灶性病变中腔体积的减少和Basso-Beattie-Bresnahan(BBB)评分被用作SCI模型大鼠功能恢复的标准。 miR-124的上调促进了NSC的分化。在NSC中转染miR-124分别显着增加了NeuN阳性细胞的百分比,并降低了体外和体内GFAP阳性细胞的百分比。用miR-124转染的NSC处理的所有大鼠均比NSC和假对照组具有更好的功能恢复。此外,用miR-124转染的NSC的全身递送导致SCI模型大鼠的病变腔体积减少。因此,miR-124的过表达可以促进NSC的分化,并在SCI的修复中起重要作用。将来,将经miR-124调节的干细胞静脉内递送至靶病变区域作为急性脊髓损伤的前瞻性治疗方法非常有用。

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