首页> 美国卫生研究院文献>Experimental Molecular Medicine >Notch ligand Jagged1 promotes mesenchymal stromal cell-based cartilage repair
【2h】

Notch ligand Jagged1 promotes mesenchymal stromal cell-based cartilage repair

机译:Notch配体Jagged1促进基于间质基质细胞的软骨修复

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Placenta-derived mesenchymal stromal cells (PMSCs) provide a promising cell source for tissue regeneration. However, rapid induction of PMSC chondrogenic differentiation during therapeutic transplantation remains extremely challenging. Here we undertook a study to determine if Notch inhibition by soluble Jagged1 (JAG1) peptides could be utilized to accelerate PMSC-induced cartilage regeneration in a mouse post-traumatic osteoarthritis (PTOA) model. Our results showed that treatment of PMSCs with soluble JAG1 significantly enhanced chondrogenesis in culture as shown by increased alcian blue staining and decreased Notch target Hes1 expression when compared to those in lgG-treated control cells. Importantly, significantly enhanced cartilage formation and decreased joint inflammation were observed when JAG1-treated PMSCs were injected into mouse PTOA knee joints. Finally, in vivo cell tracing showed that more JAG1-treated PMSCs remained in knee joint tissues and that JAG1-treated PMSCs exhibited greater PMSC chondrogenic differentiation than lgG-treated control PMSCs at 4 weeks after injection. These data indicate that transient Notch inhibition by soluble JAG1 could be used to enhance PMSC survival and chondrogenic differentiation, thereby increasing the therapeutic potential of PMSCs for cartilage regeneration.
机译:胎盘来源的间充质基质细胞(PMSC)为组织再生提供了有希望的细胞来源。但是,在治疗性移植过程中快速诱导PMSC软骨分化仍然是极具挑战性的。在这里,我们进行了一项研究,以确定是否可利用可溶的Jagged1(JAG1)肽对Notch进行抑制,以在小鼠创伤后骨关节炎(PTOA)模型中加速PMSC诱导的软骨再生。我们的结果表明,与lgG处理的对照细胞相比,用可溶性JAG1处理PMSCs可以显着增强培养物中的软骨形成,如增加的阿尔辛蓝染色和降低的Notch靶点Hes1表达所示。重要的是,当将经JAG1处理的PMSC注射到小鼠PTOA膝关节中时,观察到软骨形成明显增强,关节炎症降低。最后,体内细胞追踪显示在注射后4周,膝关节组织中残留有更多的JAG1处理的PMSC,并且与IgG处理的对照PMSC相比,JAG1处理的PMSC表现出更大的PMSC软骨分化。这些数据表明,可溶JAG1对Notch的瞬时抑制作用可用于增强PMSC的存活和软骨形成分化,从而增加PMSC在软骨再生中的治疗潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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