首页> 外文期刊>Journal of Molecular Neuroscience: MN >Mesenchymal Stem Cells Form 3D Clusters Following Intraventricular Transplantation
【24h】

Mesenchymal Stem Cells Form 3D Clusters Following Intraventricular Transplantation

机译:间充质干细胞形成脑内移植后3D簇

获取原文
获取原文并翻译 | 示例
           

摘要

Mesenchymal stem cells (MSCs) are regarded as an immune privileged cell type with numerous regeneration-promoting effects. The in vivo behavior of MSC and underlying mechanisms leading to their regenerative effects are largely unknown. The aims of this study were to comparatively investigate the in vivo behavior of canine (cMSC), human (hMSC), and murine MSC (mMSC) following intra-cerebroventricular transplantation. At 7 days post transplantation (dpt), clusters of cMSC, hMSC, and mMSC were detected within the ventricular system. At 49 dpt, cMSC-transplanted mice showed clusters mostly consisting of extracellular matrix lacking transplanted MSC. Similarly, hMSC-transplanted mice lacked MSC clusters at 49 dpt. Xenogeneic MSC transplantation was associated with a local T lymphocyte-dominated immune reaction at both time points. Interestingly, no associated inflammation was observed following syngeneic mMSC transplantation. In conclusion, transplanted MSC formed intraventricular cell clusters and exhibited a short life span in vivo. Xenogeneically in contrast to syngeneically transplanted MSC triggered a T cell-mediated graft rejection indicating that MSCs are not as immune privileged as previously assumed. However, MSC may mediate their effects by a "hit and run" mechanism and future studies will show whether syngeneically or xenogeneically transplanted MSCs exert better therapeutic effects in animals with CNS disease.
机译:间充质干细胞(MSCs)被认为是具有许多再生促进效果的免疫特征细胞类型。 MSC的体内行为和导致其再生效应的潜在机制在很大程度上是未知的。该研究的目的是在脑内移植内犬(CMSC),人(HMSC),人(HMSC)和鼠MSC(MMSC)的体内行为相对调查。在移植后7天,在心室系统内检测到CMSC,HMSC和MMSC的簇。在49个DPT,CMSC移植的小鼠显示簇,主要由缺乏移植的MSC的细胞外基质组成。类似地,HMSC移植的小鼠缺少49个DPT的MSC簇。在两个时间点,异种MSC移植与局部T淋巴细胞主导的免疫反应相关。有趣的是,在同联的MMSC移植后没有观察到相关的炎症。总之,移植的MSC形成腔内细胞簇,并在体内展示了短的寿命。与引发同映射的MSC相反,触发了T细胞介导的移植物抑制,表明MSCs不是如前所述的免疫特征。然而,MSC可以通过“命中和运行”机制和未来的研究介绍它们的效果,并表明在具有CNS病的动物中是否会对动物产生更好的治疗作用。

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