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Neuroprotective Effects of Oligodendrocyte Progenitor Cell Transplantation in Premature Rat Brain following Hypoxic-Ischemic Injury

机译:缺氧缺血性损伤后少突胶质祖细胞移植对大鼠脑的神经保护作用

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摘要

Periventricular leukomalacia (PVL) is a common ischemic brain injury in premature infants for which there is no effective treatment. The objective of this study was to determine whether transplanted mouse oligodendrocyte progenitor cells (OPCs) have neuroprotective effects in a rat model of PVL. Hypoxia-ischemia (HI) was induced in 3-day-old rat pups by left carotid artery ligation, followed by exposure to 6% oxygen for 2.5 h. Animals were assigned to OPC transplantation or sham control groups and injected with OPCs or PBS, respectively, and sacrificed up to 6 weeks later for immunohistochemical analysis to investigate the survival and differentiation of transplanted OPCs. Apoptosis was evaluated by double immunolabeling of brain sections for caspase-3 and neuronal nuclei (NeuN), while proliferation was assessed using a combination of anti-Nestin and -bromodeoxyuridine antibodies. The expression of brain-derived neurotrophic factor (BDNF) and Bcl-2 was examined 7 days after OPC transplantation. The Morris water maze was used to test spatial learning and memory. The results showed that transplanted OPCs survived and formed a myelin sheath, and stimulated BDNF and Bcl-2 expression and the proliferation of neural stem cells (NSC), while inhibiting HI-induced neuronal apoptosis relative to control animals. Moreover, deficits in spatial learning and memory resulting from HI were improved by OPC transplantation. These results demonstrate an important neuroprotective role for OPCs that can potentially be exploited in cell-based therapeutic approaches to minimize HI-induced brain injury.
机译:脑室周围白质软化(PVL)是早产儿常见的缺血性脑损伤,目前尚无有效的治疗方法。这项研究的目的是确定移植的小鼠少突胶质细胞祖细胞(OPC)在PVL大鼠模型中是否具有神经保护作用。通过结扎左颈动脉,然后暴露于6%的氧气2.5 h,在3天大的幼崽中诱发缺氧缺血(HI)。将动物分为OPC移植组或假对照组,分别注射OPCs或PBS,并在长达6周后处死以进行免疫组织化学分析,以研究移植的OPC的存活和分化。通过对caspase-3和神经元核(NeuN)的脑切片进行双重免疫标记来评估细胞凋亡,同时使用抗Nestin和-bromodeoxyuridine抗体联合评估增殖。 OPC移植后7天检查脑源性神经营养因子(BDNF)和Bcl-2的表达。莫里斯水迷宫用于测试空间学习和记忆。结果表明,移植的OPCs存活并形成髓鞘,并刺激BDNF和Bcl-2表达以及神经干细胞(NSC)的增殖,同时相对于对照动物而言抑制了HI诱导的神经元凋亡。此外,OP移植可改善由HI引起的空间学习和记忆障碍。这些结果表明,OPC具有重要的神经保护作用,可以在基于细胞的治疗方法中利用它来最大限度地减少HI引起的脑损伤。

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