• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用 iPSC 平台探索运动神经元疾病。

Exploring Motor Neuron Diseases Using iPSC Platforms.

机构信息

Department of Neurology, Johns Hopkins University, Baltimore, MD, USA.

出版信息

Stem Cells. 2022 Mar 3;40(1):2-13. doi: 10.1093/stmcls/sxab006.

DOI:10.1093/stmcls/sxab006
PMID:35511862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9199844/
Abstract

The degeneration of motor neurons is a pathological hallmark of motor neuron diseases (MNDs), but emerging evidence suggests that neuronal vulnerability extends well beyond this cell subtype. The ability to assess motor function in the clinic is limited to physical examination, electrophysiological measures, and tissue-based or neuroimaging techniques which lack the resolution to accurately assess neuronal dysfunction as the disease progresses. Spinal muscular atrophy (SMA), spinal and bulbar muscular atrophy (SBMA), hereditary spastic paraplegia (HSP), and amyotrophic lateral sclerosis (ALS) are all MNDs with devastating clinical outcomes that contribute significantly to disease burden as patients are no longer able to carry out normal activities of daily living. The critical need to accurately assess the cause and progression of motor neuron dysfunction, especially in the early stages of those diseases, has motivated the use of human iPSC-derived motor neurons (hiPSC-MN) to study the neurobiological mechanisms underlying disease pathogenesis and to generate platforms for therapeutic discovery and testing. As our understanding of MNDs has grown, so too has our need to develop more complex in vitro models which include hiPSC-MN co-cultured with relevant non-neuronal cells in 2D as well as in 3D organoid and spheroid systems. These more complex hiPSC-derived culture systems have led to the implementation of new technologies, including microfluidics, multielectrode array, and machine learning which offer novel insights into the functional correlates of these emerging model systems.

摘要

运动神经元的退化是运动神经元疾病(MNDs)的病理学标志,但新出现的证据表明,神经元易损性远远超出了这种细胞亚型。在临床上评估运动功能的能力仅限于体格检查、电生理测量以及基于组织或神经影像学的技术,这些技术缺乏分辨率,无法准确评估疾病进展过程中的神经元功能障碍。脊髓性肌萎缩症(SMA)、脊髓和延髓肌萎缩症(SBMA)、遗传性痉挛性截瘫(HSP)和肌萎缩侧索硬化症(ALS)都是 MNDs,其临床结局具有破坏性,会极大地加重疾病负担,因为患者不再能够进行正常的日常生活活动。准确评估运动神经元功能障碍的原因和进展的迫切需要,特别是在这些疾病的早期阶段,这促使人们使用人诱导多能干细胞衍生的运动神经元(hiPSC-MN)来研究疾病发病机制的神经生物学机制,并为治疗发现和测试生成平台。随着我们对 MNDs 的理解不断加深,我们也越来越需要开发更复杂的体外模型,包括 hiPSC-MN 与相关非神经元细胞在二维以及三维类器官和球体系统中的共培养。这些更复杂的 hiPSC 衍生培养系统已经引入了新技术,包括微流控、多电极阵列和机器学习,这些技术为这些新兴模型系统的功能相关性提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/9199844/5a30c4404642/sxab006_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/9199844/5a30c4404642/sxab006_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/9199844/5a30c4404642/sxab006_fig3.jpg

相似文献

1
Exploring Motor Neuron Diseases Using iPSC Platforms.利用 iPSC 平台探索运动神经元疾病。
Stem Cells. 2022 Mar 3;40(1):2-13. doi: 10.1093/stmcls/sxab006.
2
Genetic architecture of motor neuron diseases.运动神经元病的遗传结构。
J Neurol Sci. 2022 Mar 15;434:120099. doi: 10.1016/j.jns.2021.120099. Epub 2021 Dec 22.
3
RNA dysregulation in diseases of motor neurons.RNA 失调与运动神经元疾病。
Annu Rev Pathol. 2012;7:323-52. doi: 10.1146/annurev-pathol-011110-130307. Epub 2011 Oct 24.
4
Altered SYNJ2BP-mediated mitochondrial-ER contacts in motor neuron disease.运动神经元疾病中线粒体-内质网接触的 SYNJ2BP 改变。
Neurobiol Dis. 2022 Oct 1;172:105832. doi: 10.1016/j.nbd.2022.105832. Epub 2022 Jul 27.
5
Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs.通过对源自疾病特异性 iPSC 的纯化运动神经元进行全基因组转录组分析,揭示脊髓延髓肌萎缩症中的突触病理学。
Mol Brain. 2020 Feb 19;13(1):18. doi: 10.1186/s13041-020-0561-1.
6
Established Stem Cell Model of Spinal Muscular Atrophy Is Applicable in the Evaluation of the Efficacy of Thyrotropin-Releasing Hormone Analog.已建立的脊髓性肌萎缩症干细胞模型可用于评估促甲状腺激素释放激素类似物的疗效。
Stem Cells Transl Med. 2016 Feb;5(2):152-63. doi: 10.5966/sctm.2015-0059. Epub 2015 Dec 18.
7
Enhancing survival motor neuron expression extends lifespan and attenuates neurodegeneration in mutant TDP-43 mice.增强存活运动神经元表达可延长突变型TDP - 43小鼠的寿命并减轻神经退行性变。
Hum Mol Genet. 2016 Sep 15;25(18):4080-4093. doi: 10.1093/hmg/ddw247. Epub 2016 Jul 27.
8
Fishing for causes and cures of motor neuron disorders.探寻运动神经元疾病的病因及治疗方法。
Dis Model Mech. 2014 Jul;7(7):799-809. doi: 10.1242/dmm.015719.
9
Cross-sectional and longitudinal assessment of the upper cervical spinal cord in motor neuron disease.运动神经元病中颈上脊髓的横断和纵向评估。
Neuroimage Clin. 2019;24:101984. doi: 10.1016/j.nicl.2019.101984. Epub 2019 Aug 16.
10
Cellular and molecular approaches to motor neuron therapy in amyotrophic lateral sclerosis and spinal muscular atrophy.细胞和分子方法治疗肌萎缩侧索硬化症和脊髓性肌萎缩症中的运动神经元。
Neurosci Lett. 2012 Oct 11;527(2):78-84. doi: 10.1016/j.neulet.2012.04.079. Epub 2012 May 8.

引用本文的文献

1
BMP, MEK, and WNT inhibition with NGN2 expression for rapid generation of hiPSC-derived neurons amenable to regional patterning.通过抑制BMP、MEK和WNT并表达NGN2来快速生成适合区域模式化的人诱导多能干细胞衍生神经元。
Stem Cell Reports. 2025 Jul 8;20(7):102539. doi: 10.1016/j.stemcr.2025.102539. Epub 2025 Jun 19.
2
Electrophysiological characterization of sourced human iPSC-derived motor neurons.来源的人诱导多能干细胞衍生运动神经元的电生理特性
Channels (Austin). 2025 Dec;19(1):2480713. doi: 10.1080/19336950.2025.2480713. Epub 2025 Mar 25.
3
Building consensus on the application of organoid-based drug sensitivity testing in cancer precision medicine and drug development.

本文引用的文献

1
Human amyotrophic lateral sclerosis excitability phenotype screen: Target discovery and validation.人类肌萎缩侧索硬化兴奋性表型筛选:靶点发现与验证。
Cell Rep. 2021 Jun 8;35(10):109224. doi: 10.1016/j.celrep.2021.109224.
2
Human motor units in microfluidic devices are impaired by FUS mutations and improved by HDAC6 inhibition.微流控装置中的人类运动单位会受到 FUS 突变的影响,而受到 HDAC6 抑制的改善。
Stem Cell Reports. 2021 Sep 14;16(9):2213-2227. doi: 10.1016/j.stemcr.2021.03.029. Epub 2021 Apr 22.
3
Advancing Drug Discovery for Neurological Disorders Using iPSC-Derived Neural Organoids.
就类器官为基础的药物敏感性测试在癌症精准医疗和药物研发中的应用达成共识。
Theranostics. 2024 May 27;14(8):3300-3316. doi: 10.7150/thno.96027. eCollection 2024.
4
Induced Pluripotent Stem Cells and Organoids in Advancing Neuropathology Research and Therapies.诱导多能干细胞和类器官在推进神经病理学研究和治疗中的应用。
Cells. 2024 Apr 25;13(9):745. doi: 10.3390/cells13090745.
5
Disease related changes in ATAC-seq of iPSC-derived motor neuron lines from ALS patients and controls.ALS 患者和对照者 iPSC 衍生运动神经元系 ATAC-seq 的疾病相关变化。
Nat Commun. 2024 May 2;15(1):3606. doi: 10.1038/s41467-024-47758-8.
6
In Vitro Models of Amyotrophic Lateral Sclerosis.体外肌萎缩侧索硬化症模型。
Cell Mol Neurobiol. 2023 Nov;43(8):3783-3799. doi: 10.1007/s10571-023-01423-8. Epub 2023 Oct 23.
7
Using Human-Induced Pluripotent Stem Cell Derived Neurons on Microelectrode Arrays to Model Neurological Disease: A Review.利用微电极阵列上的人诱导多能干细胞衍生神经元对神经疾病进行建模:综述。
Adv Sci (Weinh). 2023 Nov;10(33):e2301828. doi: 10.1002/advs.202301828. Epub 2023 Oct 20.
8
Therapeutic targeting of ALS pathways: Refocusing an incomplete picture.治疗肌萎缩侧索硬化症相关通路:重新聚焦不完整的画面。
Ann Clin Transl Neurol. 2023 Nov;10(11):1948-1971. doi: 10.1002/acn3.51887. Epub 2023 Aug 28.
9
Differentiation of peripheral sensory neurons from iPSCs derived from stem cells from human exfoliated deciduous teeth (SHED).从人脱落乳牙干细胞(SHED)来源的诱导多能干细胞分化外周感觉神经元。
Front Cell Dev Biol. 2023 Jul 13;11:1203503. doi: 10.3389/fcell.2023.1203503. eCollection 2023.
10
Enhanced axonal regeneration of ALS patient iPSC-derived motor neurons harboring SOD1 mutation.携带有 SOD1 突变的 ALS 患者 iPSC 衍生运动神经元的增强轴突再生。
Sci Rep. 2023 Apr 5;13(1):5597. doi: 10.1038/s41598-023-31720-7.
利用 iPSC 衍生的神经类器官推进神经紊乱药物研发。
Int J Mol Sci. 2021 Mar 6;22(5):2659. doi: 10.3390/ijms22052659.
4
HDAC6 inhibition restores TDP-43 pathology and axonal transport defects in human motor neurons with TARDBP mutations.组蛋白去乙酰化酶 6 抑制可恢复 TARDBP 突变的人运动神经元中的 TDP-43 病理学和轴突运输缺陷。
EMBO J. 2021 Apr 1;40(7):e106177. doi: 10.15252/embj.2020106177. Epub 2021 Mar 10.
5
Prediction Model of Amyotrophic Lateral Sclerosis by Deep Learning with Patient Induced Pluripotent Stem Cells.基于患者诱导多能干细胞的深度学习预测肌萎缩侧索硬化症模型。
Ann Neurol. 2021 Jun;89(6):1226-1233. doi: 10.1002/ana.26047. Epub 2021 Feb 25.
6
A directional 3D neurite outgrowth model for studying motor axon biology and disease.用于研究运动轴突生物学和疾病的定向 3D 神经突生长模型。
Sci Rep. 2021 Jan 22;11(1):2080. doi: 10.1038/s41598-021-81335-z.
7
Advances in Central Nervous System Organoids: A Focus on Organoid-Based Models for Motor Neuron Disease.中枢神经系统类器官的研究进展:聚焦基于类器官的运动神经元疾病模型。
Tissue Eng Part C Methods. 2021 Mar;27(3):213-224. doi: 10.1089/ten.TEC.2020.0337. Epub 2021 Mar 3.
8
Cross-Comparison of Human iPSC Motor Neuron Models of Familial and Sporadic ALS Reveals Early and Convergent Transcriptomic Disease Signatures.家族性和散发性肌萎缩侧索硬化症的人诱导多能干细胞运动神经元模型的交叉比较揭示了早期和趋同的转录组疾病特征。
Cell Syst. 2021 Feb 17;12(2):159-175.e9. doi: 10.1016/j.cels.2020.10.010. Epub 2020 Dec 30.
9
Generation of Functional Human 3D Cortico-Motor Assembloids.生成功能性人类三维皮质运动组合体。
Cell. 2020 Dec 23;183(7):1913-1929.e26. doi: 10.1016/j.cell.2020.11.017. Epub 2020 Dec 16.
10
Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia.星形胶质细胞中的脂质代谢受损是遗传性痉挛性截瘫皮质投射神经元变性的基础。
Acta Neuropathol Commun. 2020 Dec 7;8(1):214. doi: 10.1186/s40478-020-01088-0.