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Effects of Olig2-Overexpressing Neural Stem Cells and Myelin Basic Protein-Activated T Cells on Recovery from Spinal Cord Injury

机译:Olig2过表达的神经干细胞和髓磷脂碱性蛋白激活的T细胞对脊髓损伤恢复的影响

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摘要

Neural stem cell (NSC) transplantation is a major focus of current research for treatment of spinal cord injury (SCI). However, it is very important to promote the survival and differentiation of NSCs into myelinating oligodendrocytes (OLs). In this study, myelin basic protein-activated T (MBP-T) cells were passively immunized to improve the SCI microenvironment. Olig2-overexpressing NSCs were infected with a lentivirus carrying the enhanced green fluorescent protein (GFP) reporter gene to generate Olig2-GFP-NSCs that were transplanted into the injured site to differentiate into OLs. Transferred MBP-T cells infiltrated the injured spinal cord, produced neurotrophic factors, and induced the differentiation of resident microglia and/or infiltrating blood monocytes into an “alternatively activated” anti-inflammatory macrophage phenotype by producing interleukin-13. As a result, the survival of transplanted NSCs increased fivefold in MBP-T cell-transferred rats compared with that of the vehicle-treated control. In addition, the differentiation of MBP-positive OLs increased 12-fold in Olig2-GFP-NSC-transplanted rats compared with that of GFP-NSC-transplanted controls. In the MBP-T cell and Olig2-GFP-NSC combined group, the number of OL-remyelinated axons significantly increased compared with those of all other groups. However, a significant decrease in spinal cord lesion volume and an increase in spared myelin and behavioral recovery were observed in Olig2-NSC- and NSC-transplanted MBP-T cell groups. Collectively, these results suggest that MBP-T cell adoptive immunotherapy combined with NSC transplantation has a synergistic effect on histological and behavioral improvement after traumatic SCI. Although Olig2 overexpression enhances OL differentiation and myelination, the effect on functional recovery may be surpassed by MBP-T cells.Electronic supplementary materialThe online version of this article (doi:10.1007/s13311-011-0090-9) contains supplementary material, which is available to authorized users.
机译:神经干细胞(NSC)移植是当前治疗脊髓损伤(SCI)的主要研究重点。但是,促进NSC存活和分化为有髓鞘的少突胶质细胞(OL)非常重要。在这项研究中,髓磷脂碱性蛋白激活的T(MBP-T)细胞被被动免疫以改善SCI微环境。用携带增强的绿色荧光蛋白(GFP)报告基因的慢病毒感染过表达Olig2的NSC,以产生Olig2-GFP-NSC,然后将其移植到受伤部位以分化为OL。转移的MBP-T细胞渗入受伤的脊髓,产生神经营养因子,并通过产生白介素13诱导驻留的小胶质细胞和/或浸润的血液单核细胞分化为“另一种激活的”抗炎巨噬细胞表型。结果,与用媒介物处理的对照组相比,在MBP-T细胞转移的大鼠中移植的NSCs的存活增加了五倍。另外,与GFP-NSC移植的对照相比,在Olig2-GFP-NSC移植的大鼠中MBP阳性OL的分化增加了12倍。与所有其他组相比,在MBP-T细胞和Olig2-GFP-NSC联合组中,OL-髓鞘再生的轴突的数量显着增加。但是,在Olig2-NSC和NSC移植的MBP-T细胞组中,观察到脊髓病变体积显着减少,备用髓磷脂和行为恢复增加。总体而言,这些结果表明,MBP-T细胞过继免疫疗法与NSC移植相结合,对SCI创伤后的组织学和行为学改善具有协同作用。尽管Olig2的过表达增强了OL的分化和髓鞘形成,但MBP-T细胞可能超过了其对功能恢复的作用。电子补充材料本文的在线版本(doi:10.1007 / s13311-011-0090-9)包含补充材料,该材料是可供授权用户使用。

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