首页> 外文期刊>Stem Cell Reports >Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury
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Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury

机译:软骨素酶ABC交付人类少突胶质神经祖细胞促进慢性脊髓损伤的功能修复。

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SummaryTreatment of chronic spinal cord injury (SCI) is challenging due to cell loss, cyst formation, and the glial scar. Previously, we reported on the therapeutic potential of a neural progenitor cell (NPC) and chondroitinase ABC (ChABC) combinatorial therapy for chronic SCI. However, the source of NPCs and delivery system required for ChABC remained barriers to clinical application. Here, we investigated directly reprogrammed human NPCs biased toward an oligodendrogenic fate (oNPCs) in combination with sustained delivery of ChABC using an innovative affinity release strategy in a crosslinked methylcellulose biomaterial for the treatment of chronic SCI in an immunodeficient rat model. This combinatorial therapy increased long-term survival of oNPCs around the lesion epicenter, facilitated greater oligodendrocyte differentiation, remyelination of the spared axons by engrafted oNPCs, enhanced synaptic connectivity with anterior horn cells and neurobehavioral recovery. This combinatorial therapy is a promising strategy to regenerate the chronically injured spinal cord.
机译:总结由于细胞丢失,囊肿形成和神经胶质瘢痕,慢性脊髓损伤(SCI)的治疗具有挑战性。以前,我们报道了神经祖细胞(NPC)和软骨素酶ABC(ChABC)联合治疗慢性SCI的治疗潜力。然而,ChABC所需的NPC来源和递送系统仍然是临床应用的障碍。在这里,我们研究了在重交联甲基纤维素生物材料中使用创新的亲和力释放策略,将重编程的人NPC偏向寡树突状结局(oNPC)与ChABC的持续递送相结合,以治疗免疫缺陷大鼠模型中的慢性SCI。这种联合疗法增加了病变中心附近的oNPC的长期存活率,促进了更大的少突胶质细胞分化,通过植入的oNPC使多余的轴突重新髓鞘化,增强了与前角细胞的突触连接性以及神经行为恢复。这种组合疗法是使慢性受伤的脊髓再生的有希望的策略。

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