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Time-dependent changes in the microenvironment of injured spinal cord affects the therapeutic potential of neural stem cell transplantation for spinal cord injury

机译:脊髓损伤的微环境随时间变化会影响神经干细胞移植治疗脊髓损伤的治疗潜力

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Background The transplantation of neural stem/progenitor cells (NS/PCs) at the sub-acute phase of spinal cord injury, but not at the chronic phase, can promote functional recovery. However, the reasons for this difference and whether it involves the survival and/or fate of grafted cells under these two conditions remain unclear. To address this question, NS/PC transplantation was performed after contusive spinal cord injury in adult mice at the sub-acute and chronic phases. Results Quantitative analyses using bio-imaging, which can noninvasively detect surviving grafted cells in living animals, revealed no significant difference in the survival rate of grafted cells between the sub-acute and chronic transplantation groups. Additionally, immunohistology revealed no significant difference in the differentiation phenotypes of grafted cells between the two groups. Microarray analysis revealed no significant differences in the expression of genes encoding inflammatory cytokines or growth factors, which affect the survival and/or fate of grafted cells, in the injured spinal cord between the sub-acute and chronic phases. By contrast, the distribution of chronically grafted NS/PCs was restricted compared to NS/PCs grafted at the sub-acute phase because a more prominent glial scar located around the lesion epicenter enclosed the grafted cells. Furthermore, microarray and histological analysis revealed that the infiltration of macrophages, especially M2 macrophages, which have anti-inflammatory role, was significantly higher at the sub-acute phase than the chronic phase. Ultimately, NS/PCs that were transplanted in the sub-acute phase, but not the chronic phase, promoted functional recovery compared with the vehicle control group. Conclusions The extent of glial scar formation and the characteristics of inflammation is the most remarkable difference in the injured spinal cord microenvironment between the sub-acute and chronic phases. To achieve functional recovery by NS/PC transplantation in cases at the chronic phase, modification of the microenvironment of the injured spinal cord focusing on glial scar formation and inflammatory phenotype should be considered.
机译:背景技术在脊髓损伤的亚急性阶段而非慢性阶段,神经干/祖细胞(NS / PC)的移植可以促进功能恢复。然而,这种差异的原因以及在这两种条件下是否涉及移植细胞的存活和/或命运仍不清楚。为了解决这个问题,成年小鼠在急性和慢性期挫伤性脊髓损伤后进行了NS / PC移植。结果使用生物成像技术进行的定量分析可以无创地检测活体动物中存活的移植细胞,结果显示亚急性移植组和慢性移植组之间的移植细胞存活率没有显着差异。另外,免疫组织学显示两组之间的移植细胞的分化表型没有显着差异。基因芯片分析显示,在亚急性和慢性期受损脊髓中,编码炎症细胞因子或生长因子的基因的表达无明显差异,这些基因影响移植细胞的存活和/或命运。相比之下,与亚急性期移植的NS / PC相比,长期移植的NS / PC的分布受到限制,因为位于病灶震中周围的更明显的神经胶质瘢痕包围了移植的细胞。此外,微阵列和组织学分析显示,具有抗炎作用的巨噬细胞,特别是M2巨噬细胞的浸润在亚急性期显着高于慢性期。最终,与媒介物对照组相比,亚急性期而非慢性期移植的NS / PC促进了功能恢复。结论胶质瘢痕形成的程度和炎症的特征是亚急性期和慢性期在受损的脊髓微环境中的最显着差异。为了在慢性期通过NS / PC移植实现功能恢复,应考虑对损伤脊髓的微环境进行修饰,重点是神经胶质瘢痕形成和炎性表型。

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