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Development of a Model of Sacrocaudal Spinal Cord Injury in Cloned Yucatan MiniPigs for Cellular Transplantation Research

机译:克隆的尤加坦微型猪of尾脊髓损伤模型的建立用于细胞移植研究

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摘要

Research into transplantation strategies to treat spinal cord injury (SCI) is frequently performed in rodents, but translation of results to clinical patients can be poor and a large mammalian model of severe SCI is needed. The pig has been considered an optimal model species in which to perform preclinical testing, and the Yucatan minipig can be cloned successfully utilizing somatic cell nuclear transfer (SCNT). However, induction of paralysis in pigs poses significant welfare and nursing challenges. The present study was conducted to determine whether Yucatan SCNT clones could be used to develop an SCI animal model for cellular transplantation research. First, we demonstrated that transection of the sacrocaudal spinal cord in Yucatan SCNT clones produces profound, quantifiable neurological deficits restricted to the tail. We then established that neurospheres could be isolated from brain tissue of green fluorescence protein (GFP) transfected SCNT clones. Finally, we confirmed survival of transplanted GFP-expressing neural stem cells in the SCI lesion and their differentiation into glial and neuronal lineages for up to 4 weeks without immunosuppression. We conclude that this model of sacrocaudal SCI in Yucatan SCNT clones represents a powerful research tool to investigate the effect of cellular transplantation on axonal regeneration and functional recovery.
机译:在啮齿动物中经常进行对治疗脊髓损伤(SCI)的移植策略的研究,但对临床患者的结果翻译可能很差,因此需要大型哺乳动物模型来研究严重SCI。猪被认为是进行临床前测试的最佳模型物种,尤卡坦小型猪可以利用体细胞核移植(SCNT)成功克隆。然而,诱发猪瘫痪带来了重大的福利和护理挑战。进行本研究以确定是否可以将尤加坦SCNT克隆用于开发用于细胞移植研究的SCI动物模型。首先,我们证明了尤卡坦半岛SCNT克隆中的ac骨脊髓横断产生了严重的,可量化的神经缺陷,仅限于尾巴。然后,我们确定可以从绿色荧光蛋白(GFP)转染的SCNT克隆的脑组织中分离神经球。最后,我们确认了移植的表达GFP的神经干细胞在SCI病变中的存活,并且在不进行免疫抑制的情况下,可以分化为神经胶质和神经元谱系长达4周。我们得出的结论是,尤卡坦州SCNT克隆中的ac尾SCI模型代表了一个强大的研究工具,可用来研究细胞移植对轴突再生和功能恢复的影响。

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