direct reprogramming as a therapeutic strategy for brain and retina repair.
作者信息
Sekiryu Haruka, Matsuda Taito
机构信息
Department of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
出版信息
Neural Regen Res. 2021 Oct;16(10):1998-1999. doi: 10.4103/1673-5374.308093.
Abstract
摘要
相似文献
1
direct reprogramming as a therapeutic strategy for brain and retina repair.直接重编程作为脑和视网膜修复的治疗策略。
Neural Regen Res. 2021 Oct;16(10):1998-1999. doi: 10.4103/1673-5374.308093.
2
Neuronal Reprogramming for Tissue Repair and Neuroregeneration.神经重编程用于组织修复和神经再生。
Int J Mol Sci. 2020 Jun 16;21(12):4273. doi: 10.3390/ijms21124273.
3
Potentials of Cellular Reprogramming as a Novel Strategy for Neuroregeneration.细胞重编程作为神经再生新策略的潜力
Front Cell Neurosci. 2018 Nov 30;12:460. doi: 10.3389/fncel.2018.00460. eCollection 2018.
4
Neuronal Reprogramming for Brain Repair: Challenges and Perspectives.神经元重编程用于脑修复：挑战与展望。
Trends Mol Med. 2020 Oct;26(10):890-892. doi: 10.1016/j.molmed.2020.08.006. Epub 2020 Sep 14.
5
Corrigendum: Potentials of Cellular Reprogramming as a Novel Strategy for Neuroregeneration.勘误：细胞重编程作为神经再生新策略的潜力。
Front Cell Neurosci. 2019 May 3;13:147. doi: 10.3389/fncel.2019.00147. eCollection 2019.
6
Brain repair from intrinsic cell sources: Turning reactive glia into neurons.源自内在细胞源的脑修复：将反应性胶质细胞转化为神经元。
Prog Brain Res. 2017;230:69-97. doi: 10.1016/bs.pbr.2016.12.010. Epub 2017 Feb 7.
7
Partial reprogramming as a therapeutic approach for heart disease: A state-of-the-art review.部分重编程作为心脏病的治疗方法：最新综述。
J Cell Biochem. 2019 Sep;120(9):14247-14261. doi: 10.1002/jcb.28900. Epub 2019 May 12.
8
In Vivo Reprogramming for Brain and Spinal Cord Repair.体内重编程用于脑和脊髓修复。
eNeuro. 2015 Nov 9;2(5). doi: 10.1523/ENEURO.0106-15.2015. eCollection 2015 Sep-Oct.
9
Brain repair and reprogramming: the route to clinical translation.脑修复与重编程：通往临床转化之路。
J Intern Med. 2016 Sep;280(3):265-75. doi: 10.1111/joim.12475.
10
Direct Lineage Reprogramming for Brain Repair: Breakthroughs and Challenges.直接谱系重编程用于脑修复：突破与挑战。
Trends Mol Med. 2019 Oct;25(10):897-914. doi: 10.1016/j.molmed.2019.06.006. Epub 2019 Jul 29.
引用本文的文献
1
Co-administration of extracellular matrix-based biomaterials with neural stem cell transplantation for treatment of central nervous system injury.基于细胞外基质的生物材料与神经干细胞移植联合应用治疗中枢神经系统损伤
Front Neurosci. 2023 May 15;17:1177040. doi: 10.3389/fnins.2023.1177040. eCollection 2023.
2
astrocyte-to-neuron reprogramming for central nervous system regeneration: a narrative review.用于中枢神经系统再生的星形胶质细胞向神经元重编程：一篇叙述性综述。
Neural Regen Res. 2023 Apr;18(4):750-755. doi: 10.4103/1673-5374.353482.
3
Sonoporation-Mediated Gene Transfection: A Novel Direction for Cell Reprogramming .超声穿孔介导的基因转染：细胞重编程的新方向
Front Bioeng Biotechnol. 2022 Jan 31;9:803055. doi: 10.3389/fbioe.2021.803055. eCollection 2021.
本文引用的文献
1
Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice.通过 CRISPR-CasRx 实现胶质细胞向神经元的转化可缓解小鼠神经疾病症状。
Cell. 2020 Apr 30;181(3):590-603.e16. doi: 10.1016/j.cell.2020.03.024. Epub 2020 Apr 8.
2
Gene therapy conversion of striatal astrocytes into GABAergic neurons in mouse models of Huntington's disease.基因治疗将亨廷顿病小鼠模型纹状体星形胶质细胞转化为 GABA 能神经元。
Nat Commun. 2020 Feb 27;11(1):1105. doi: 10.1038/s41467-020-14855-3.
3
Microglia in the developing retina.发育中的视网膜中的小胶质细胞。
Neural Dev. 2019 Dec 30;14(1):12. doi: 10.1186/s13064-019-0137-x.
4
A NeuroD1 AAV-Based Gene Therapy for Functional Brain Repair after Ischemic Injury through In Vivo Astrocyte-to-Neuron Conversion.一种基于NeuroD1 的 AAV 基因治疗方法，通过体内星形胶质细胞向神经元的转化，实现缺血性损伤后的功能性大脑修复。
Mol Ther. 2020 Jan 8;28(1):217-234. doi: 10.1016/j.ymthe.2019.09.003. Epub 2019 Sep 6.
5
Inducing Different Neuronal Subtypes from Astrocytes in the Injured Mouse Cerebral Cortex.在损伤的小鼠大脑皮层中诱导星形胶质细胞分化为不同的神经元亚型。
Neuron. 2019 Sep 25;103(6):1086-1095.e5. doi: 10.1016/j.neuron.2019.08.009. Epub 2019 Sep 2.
6
Pioneer Factor NeuroD1 Rearranges Transcriptional and Epigenetic Profiles to Execute Microglia-Neuron Conversion.先驱因子 NeuroD1 重排转录和表观遗传特征以执行小胶质细胞-神经元转化。
Neuron. 2019 Feb 6;101(3):472-485.e7. doi: 10.1016/j.neuron.2018.12.010. Epub 2019 Jan 9.
7
Restoration of vision after de novo genesis of rod photoreceptors in mammalian retinas.哺乳动物视网膜中新生的杆状光感受器后视力的恢复。
Nature. 2018 Aug;560(7719):484-488. doi: 10.1038/s41586-018-0425-3. Epub 2018 Aug 15.
8
Wnt Regulates Proliferation and Neurogenic Potential of Müller Glial Cells via a Lin28/let-7 miRNA-Dependent Pathway in Adult Mammalian Retinas.Wnt通过成年哺乳动物视网膜中依赖Lin28/let-7微小RNA的途径调控米勒胶质细胞的增殖和神经源性潜能。
Cell Rep. 2016 Sep 27;17(1):165-178. doi: 10.1016/j.celrep.2016.08.078.
9
In Vivo Reprogramming for CNS Repair: Regenerating Neurons from Endogenous Glial Cells.用于中枢神经系统修复的体内重编程：从内源性神经胶质细胞再生神经元。
Neuron. 2016 Aug 17;91(4):728-738. doi: 10.1016/j.neuron.2016.08.004.
10
Hierarchical mechanisms for direct reprogramming of fibroblasts to neurons.成纤维细胞向神经元直接重编程的层次机制。
Cell. 2013 Oct 24;155(3):621-35. doi: 10.1016/j.cell.2013.09.028.
Zotero 插件