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首页> 外文期刊>Journal of tissue engineering and regenerative medicine >Human gingival mesenchymal stem cells pretreated with vesicular moringin nanostructures as a new therapeutic approach in a mouse model of spinal cord injury
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Human gingival mesenchymal stem cells pretreated with vesicular moringin nanostructures as a new therapeutic approach in a mouse model of spinal cord injury

机译:人牙龈间充质干细胞用囊泡Moringin纳米结构预处理,作为脊髓损伤小鼠模型的新治疗方法

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Abstract Spinal cord injury (SCI) is a neurological disorder that arises from a primary acute mechanical lesion, followed by a pathophysiological cascade of events that leads to further spinal cord tissue damage. Several preclinical and clinical studies have highlighted the ability of stem cell therapy to improve long‐term functional recovery in SCI. Previously, we demonstrated that moringin (MOR) treatment accelerates the differentiation process in mesenchymal stem cells inducing an early up‐regulation of neural development associated genes. In the present study, we investigated the anti‐inflammatory, anti‐apoptotic, and regenerative effects of gingival mesenchymal stem cells (GMSCs) pretreated with nanostructured liposomes enriched with MOR in an animal model of SCI. SCI was produced by extradural compression of the spinal cord at levels T6–T7 in ICR (CD‐1) mice. Animals were randomly assigned to the following groups: Sham, SCI, SCI?+?GMSCs (1?×?10 6 ?cell/i.v.), SCI?+?MOR‐GMSCs (1?×?10 6 ?cell/i.v.). Our data show that MOR‐treated GMSCs exert anti‐inflammatory and anti‐apoptotic activities. In particular, MOR‐treated GMSCs are able to reduce the spinal cord levels of COX‐2, GFAP, and inflammatory cytokines IL‐1β and IL‐6 and to restore spinal cord normal morphology. Also, MOR‐treated GMSCs influenced the apoptotic pathway, by reducing Bax, caspase 3, and caspase 9 expressions.
机译:摘要脊髓损伤(SCI)是一种神经疾病,其出现于初级急性机械病变,然后是导致进一步脊髓组织损伤的病理生理学级联。几种临床前和临床研究强调了干细胞疗法能力,以改善SCI中的长期功能恢复。此前,我们证明辣木(Mor)治疗加速了间充质干细胞中的分化过程,诱导神经发育相关基因的早期上调。在本研究中,我们研究了用纳米结构脂质体预处理的抗炎,抗凋亡和再生效果,用纳米结构脂质体在SCI的动物模型中富集。通过在ICR(CD-1)小鼠水平T6-T7水平的脊髓外脊髓的外脊髓压缩产生SCI。动物随机分配到以下组:假,SCI,SCI?+?GMSCs(1?×10 6?单元/ IV),SCI?+?MOR-GMSCs(1?×10 6?单元/ IV) 。我们的数据显示,MOR治疗的GMSCS发挥抗炎和抗凋亡活动。特别是,MOR-COMPED GMSCs能够减少COX-2,GFAP和炎症细胞因子IL-1β和IL-6的脊髓水平,并恢复脊髓正常形态。此外,MOR治疗的GMSCs通过还原Bax,Caspase 3和Caspase 9表达来影响凋亡途径。

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