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冷冻保存的人类神经元在神经退行性疾病体内疾病模型中的长期植入

Long-Term Engraftment of Cryopreserved Human Neurons for In Vivo Disease Modeling in Neurodegenerative Disease.

作者信息

Marmion David J, Deng Peter, Hiller Benjamin M, Lewis Rachel L, Harms Lisa J, Cameron David L, Nolta Jan A, Kordower Jeffrey H, Fink Kyle D, Wakeman Dustin R

机构信息

Department of Neurological Sciences, Rush University Medical Center, Chicago, IL 60612, USA.

Department of Neurobiology, Barrow Neurological Institute, Phoenix, AZ 85013, USA.

出版信息

Biology (Basel). 2025 Feb 19;14(2):217. doi: 10.3390/biology14020217.

Abstract

The transplantation of human neurons into the central nervous system (CNS) offers transformative opportunities for modeling neurodegenerative diseases in vivo. This study evaluated the survival, integration, and functional properties of cryopreserved forebrain GABAergic neurons (iGABAs) derived from human induced pluripotent stem cells (iPSCs) across three species used in translational research. iGABAs were stereotactically injected into the striatum of Sprague-Dawley rats, immunodeficient RNU rats, R6/2 Huntington's disease (HD) mice, wild-type controls, and Cynomolgus monkeys. Post-transplantation, long-term assessments revealed robust neuronal survival, extensive neurite outgrowth, and integration with host CNS environments. In immunodeficient rats, iGABAs innervated the neuraxis, extending from the prefrontal cortex to the midbrain, while maintaining mature neuronal phenotypes without uncontrolled proliferation. Similarly, grafts in nonhuman primates showed localized survival and stable phenotype at one month. In the neurodegenerative milieu of HD mice, iGABAs survived up to six months, projecting into the host striatum and white matter, with evidence of mutant huntingtin aggregates localized within the graft, indicating pathological protein transfer. These findings underscore the utility of cryopreserved iGABAs as a reproducible, scalable model for disease-specific CNS investigations and mechanistic studies of proteinopathic propagation. This work establishes a critical platform for studying neurodegenerative diseases and developing therapeutic interventions.

摘要

将人类神经元移植到中枢神经系统(CNS)为在体内模拟神经退行性疾病提供了变革性的机会。本研究评估了源自人类诱导多能干细胞(iPSC)的低温保存的前脑GABA能神经元(iGABA)在三种用于转化研究的物种中的存活、整合和功能特性。将iGABA立体定向注射到Sprague-Dawley大鼠、免疫缺陷RNU大鼠、R6/2亨廷顿舞蹈病(HD)小鼠、野生型对照和食蟹猴的纹状体中。移植后,长期评估显示神经元存活良好、神经突广泛生长并与宿主CNS环境整合。在免疫缺陷大鼠中,iGABA支配神经轴,从前额叶皮质延伸至中脑,同时维持成熟的神经元表型且无不受控制的增殖。同样,非人类灵长类动物的移植物在1个月时显示出局部存活和稳定的表型。在HD小鼠的神经退行性环境中,iGABA存活长达6个月,投射到宿主纹状体和白质中,有证据表明移植物内存在突变型亨廷顿蛋白聚集体,提示病理性蛋白质转移。这些发现强调了低温保存的iGABA作为一种可重复、可扩展的模型用于疾病特异性CNS研究和蛋白病传播机制研究的效用。这项工作为研究神经退行性疾病和开发治疗干预措施建立了一个关键平台。

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