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NeuroD1可诱导小胶质细胞凋亡,且无法诱导小胶质细胞向神经元的跨谱系重编程。

NeuroD1 induces microglial apoptosis and cannot induce microglia-to-neuron cross-lineage reprogramming.

作者信息

Rao Yanxia, Du Siling, Yang Baozhi, Wang Yuqing, Li Yuxin, Li Ruofan, Zhou Tian, Du Xiangjuan, He Yang, Wang Yafei, Zhou Xin, Yuan Ti-Fei, Mao Ying, Peng Bo

机构信息

Shanghai Key Laboratory of Psychotic Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China.

Shanghai Key Laboratory of Psychotic Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 201108, China; Department of Neurosurgery, Huashan Hospital, Institute for Translational Brain Research, State Key Laboratory of Medical Neurobiology, MOE Frontiers Center for Brain Science, Fudan University, Shanghai 200032, China.

出版信息

Neuron. 2021 Dec 15;109(24):4094-4108.e5. doi: 10.1016/j.neuron.2021.11.008. Epub 2021 Dec 6.

Abstract

The regenerative capacity of neurons is limited in the central nervous system (CNS), with irreversible neuronal loss upon insult. In contrast, microglia exhibit extraordinary capacity for repopulation. Matsuda et al. (2019) recently reported NeuroD1-induced microglia-to-neuron conversion, aiming to provide an "unlimited" source to regenerate neurons. However, the extent to which NeuroD1 can exert cross-lineage reprogramming of microglia (myeloid lineage) to neurons (neuroectodermal lineage) is unclear. In this study, we unexpectedly found that NeuroD1 cannot convert microglia to neurons in mice. Instead, NeuroD1 expression induces microglial cell death. Moreover, lineage tracing reveals non-specific leakage of similar lentiviruses as previously used for microglia-to-neuron conversion, which confounds the microglia-to-neuron observation. In summary, we demonstrated that NeuroD1 cannot induce microglia-to-neuron cross-lineage reprogramming. We here propose rigid principles for verifying glia-to-neuron conversion. This Matters Arising paper is in response to Matsuda et al. (2019), published in Neuron.

摘要

在中枢神经系统(CNS)中,神经元的再生能力有限,受损后会出现不可逆的神经元损失。相比之下,小胶质细胞表现出非凡的增殖能力。松田等人(2019年)最近报道了NeuroD1诱导的小胶质细胞向神经元的转化,旨在提供一个“无限”的神经元再生来源。然而,NeuroD1能够在多大程度上对小胶质细胞(髓系谱系)向神经元(神经外胚层谱系)进行跨谱系重编程尚不清楚。在本研究中,我们意外地发现NeuroD1在小鼠中无法将小胶质细胞转化为神经元。相反,NeuroD1表达会诱导小胶质细胞死亡。此外,谱系追踪揭示了与先前用于小胶质细胞向神经元转化的类似慢病毒的非特异性泄漏,这混淆了小胶质细胞向神经元的观察结果。总之,我们证明了NeuroD1不能诱导小胶质细胞向神经元的跨谱系重编程。我们在此提出了验证胶质细胞向神经元转化的严格原则。这篇“问题提出”论文是对发表在《神经元》杂志上的松田等人(2019年)的回应。

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