表达dlk1的神经祖细胞促进颈脊髓损伤后组织修复和功能恢复。

IF 5.4 2区 医学 Q1 CELL & TISSUE ENGINEERING
Nader Hejrati, Zijian Lou, Sogolie Kouhzaei, Oliver Zhang, Jian Wang, Mohamad Khazaei, Michael G Fehlings
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引用次数: 0

摘要

脊髓损伤(SCI)引发了一个以炎症、神经胶质瘤和信号通路中断为特征的敌对微环境,这些微环境共同阻碍神经修复。神经祖细胞(npc)是一种很有前途的再生方法,但在这种情况下,它们的存活和分化往往受到损害。在这里,我们研究了工程npc过度表达Notch通路调节剂Delta-like非规范Notch配体1 (DLK1)是否可以克服这些限制并改善大鼠颈椎脊髓损伤后的功能结局。在Pax6启动子驱动的表达系统下,设计npc表达DLK1,确保祖细胞状态下DLK1水平升高。在移植过表达dlk1的npc或对照npc后,我们在12周内评估移植物存活率、谱系分化、行为表现和电生理整合。与对照组相比,表达dlk1的npc在受损脊髓中表现出更大的保留力,并表现出增强的神经元分化和减少的星形细胞承诺。行为测试——包括前肢握力和猫步步态评估——表明,dlk1修饰的npc在前肢运动协调和整体运动方面有显著改善。与此同时,电生理记录显示,接受dlk1转导的鼻咽癌移植物的动物的运动诱发电位振幅和曲线下面积值增加,表明宿主运动电路内突触整合增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DLK1-expressing neural progenitor cells promote tissue repair and functional recovery after cervical spinal cord injury.

Spinal cord injury (SCI) elicits a hostile microenvironment characterized by inflammation, gliosis, and disrupted signaling pathways that collectively impede neural repair. Neural progenitor cells (NPCs) represent a promising regenerative approach, yet their survival and differentiation are often compromised in this setting. Here, we investigated whether engineering NPCs to overexpress the Notch pathway modulator Delta-like non-canonical Notch ligand 1 (DLK1) could overcome these limitations and improve functional outcomes after cervical SCI in rats. NPCs were engineered to express DLK1 under a Pax6 promoter-driven expression system, ensuring elevated DLK1 levels during the progenitor state. Following transplantation of DLK1-overexpressing NPCs or control NPCs, we assessed graft survival, lineage differentiation, behavioral performance, and electrophysiological integration over 12 weeks. DLK1-expressing NPCs exhibited significantly greater retention in the injured spinal cord and showed enhanced neuronal differentiation alongside reduced astrocytic commitment compared to controls. Behavioral tests-including forelimb grip strength and CatWalk gait assessments-demonstrated that DLK1-modified NPCs conferred robust improvements in forelimb motor coordination and overall locomotion. Concordantly, electrophysiological recordings revealed increased motor-evoked potential amplitudes and area-under-the-curve values in animals receiving DLK1-transduced NPC grafts, indicative of strengthened synaptic integration within the host motor circuitry.

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来源期刊
Stem Cells Translational Medicine
Stem Cells Translational Medicine CELL & TISSUE ENGINEERING-
CiteScore
12.90
自引率
3.30%
发文量
140
审稿时长
6-12 weeks
期刊介绍: STEM CELLS Translational Medicine is a monthly, peer-reviewed, largely online, open access journal. STEM CELLS Translational Medicine works to advance the utilization of cells for clinical therapy. By bridging stem cell molecular and biological research and helping speed translations of emerging lab discoveries into clinical trials, STEM CELLS Translational Medicine will help move applications of these critical investigations closer to accepted best patient practices and ultimately improve outcomes. The journal encourages original research articles and concise reviews describing laboratory investigations of stem cells, including their characterization and manipulation, and the translation of their clinical aspects of from the bench to patient care. STEM CELLS Translational Medicine covers all aspects of translational cell studies, including bench research, first-in-human case studies, and relevant clinical trials.
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