...
【24h】

Adult mesenchymal stem cells support cisplatin-treated dorsal root ganglion survival.

机译:成人间充质干细胞支持顺铂治疗的背根神经节存活。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Mesenchymal stem cells (MSCs) have been found to be useful in the management of different models of neurological diseases. In the present study, we tested the possible protective effect of MSCs on sensory dorsal root ganglia (DRG) explants exposed to the toxic effect of CDDP, a widely used anticancer drug. DRG explants cultured on a collagen layer and exposed to NGF for 2h (differentiating neurons) or for 5 days (fully differentiated neurons) were treated with CDDP and subsequently co-cultured with MSCs. MSCs were able to support the survival of both differentiating and fully differentiated DRG neurons up to 2 months after the drug treatment, reducing the CDDP-induced death of DRG neurons. MSCs were, however, unable to restore the correct length of DRG neurites compromised by CDDP treatment. The positive effect on neuronal survival was exerted through the contact between DRG and MSCs, and not mediated by neurotrophic factors released by the MSCs. Our observations could represent a starting point for designing a neuroprotective strategy to limit CDDP induced neuropathy without interfering with its anticancer properties.
机译:间充质干细胞(MSCs)已发现可用于管理不同模型的神经系统疾病。在本研究中,我们测试了MSC对暴露于CDDP(一种广泛使用的抗癌药物)的毒性作用的感觉背根神经节(DRG)外植体的可能保护作用。将在胶原层上培养并暴露于NGF 2h(分化神经元)或5天(完全分化的神经元)的DRG外植体用CDDP处理,然后与MSC共培养。 MSC能够在药物治疗后的2个月内支持分化的和完全分化的DRG神经元的存活,从而减少了CDDP诱导的DRG神经元的死亡。然而,MSC不能恢复CDDP治疗损害的DRG神经突的正确长度。对神经元存活的积极影响是通过DRG与MSC之间的接触发挥的,而不是由MSC释放的神经营养因子介导的。我们的观察结果可能是设计神经保护策略以限制CDDP诱导的神经病变而不干扰其抗癌特性的起点。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号