Using induced pluripotent stem cells derived neurons to model brain diseases

被引:29
|
作者
McKinney, Cindy E. [1 ,2 ]
机构
[1] Edward Via Coll Osteopath Med, IPSC Lab, Spartanburg, SC 29303 USA
[2] Gibbs Res Inst, Spartanburg, SC 29303 USA
关键词
induced pluripotent stem cells; neuron cell models; brain diseases; molecular mechanisms; therapeutics; translational medicine; AMYOTROPHIC-LATERAL-SCLEROSIS; FRONTOTEMPORAL DEMENTIA; CEROID-LIPOFUSCINOSIS; GENERATION; INFANTILE; THERAPY; IPSCS; CLN5;
D O I
10.4103/1673-5374.211180
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ability to use induced pluripotent stem cells (iPSC) to model brain diseases is a powerful tool for unraveling mechanistic alterations in these disorders. Rodent models of brain diseases have spurred understanding of pathology but the concern arises that they may not recapitulate the full spectrum of neuron disruptions associated with human neuropathology. iPSC derived neurons, or other neural cell types, provide the ability to access pathology in cells derived directly from a patient's blood sample or skin biopsy where availability of brain tissue is limiting. Thus, utilization of iPSC to study brain diseases provides an unlimited resource for disease modelling but may also be used for drug screening for effective therapies and may potentially be used to regenerate aged or damaged cells in the future. Many brain diseases across the spectrum of neurodevelopment, neurodegenerative and neuropsychiatric are being approached by iPSC models. The goal of an iPSC based disease model is to identify a cellular phenotype that discriminates the disease-bearing cells from the control cells. In this mini-review, the importance of iPSC cell models validated for pluripotency, germline competency and function assessments is discussed. Selected examples for the variety of brain diseases that are being approached by iPSC technology to discover or establish the molecular basis of the neuropathology are discussed.
引用
收藏
页码:1062 / 1067
页数:6
相关论文
共 50 条
  • [1] Using induced pluripotent stem cells derived neurons to model brain diseases
    Cindy E.McKinney
    Neural Regeneration Research, 2017, 12 (07) : 1062 - 1067
  • [2] Stem Cells on the Brain: Modeling Neurodevelopmental and Neurodegenerative Diseases Using Human Induced Pluripotent Stem Cells
    Srikanth, Priya
    Young-Pearse, Tracy L.
    JOURNAL OF NEUROGENETICS, 2014, 28 (1-2) : 5 - 29
  • [3] Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells
    Hayashi, Yohei
    Takami, Miho
    Matsuo-Takasaki, Mami
    FRONTIERS IN CELLULAR NEUROSCIENCE, 2020, 14
  • [4] Investigation of immune-related diseases using patient-derived induced pluripotent stem cells
    Shoda, Hirofumi
    Natsumoto, Bunki
    Fujio, Keishi
    INFLAMMATION AND REGENERATION, 2023, 43 (01)
  • [5] Cortical Neurons Derived from Equine Induced Pluripotent Stem Cells Are Susceptible to Neurotropic Flavivirus Infection and Replication: An In Vitro Model for Equine Neuropathic Diseases
    Fortuna, Patrick R. J.
    Bielefeldt-Ohmann, Helle
    Ovchinnikov, Dmitry A.
    Wolvetang, Ernst J.
    Whitworth, Deanne J.
    STEM CELLS AND DEVELOPMENT, 2018, 27 (10) : 704 - 715
  • [6] Unraveling the biology of bipolar disorder using induced pluripotent stem-derived neurons
    Miller, Nathaniel D.
    Kelsoe, John R.
    BIPOLAR DISORDERS, 2017, 19 (07) : 544 - 551
  • [7] Urine-derived induced pluripotent/neural stem cells for modeling neurological diseases
    Shi, Tianyuan
    Cheung, Martin
    CELL AND BIOSCIENCE, 2021, 11 (01)
  • [8] Research progress of autoimmune diseases based on induced pluripotent stem cells
    Ren, Rutong
    Jiang, Jinhe
    Li, Xinxin
    Zhang, Guirong
    FRONTIERS IN IMMUNOLOGY, 2024, 15
  • [9] Induced pluripotent stem cells for modelling human diseases
    Unternaehrer, Juli J.
    Daley, George Q.
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2011, 366 (1575) : 2274 - 2285
  • [10] Research on neurodegenerative diseases using induced pluripotent stem cells
    Imamura, Keiko
    Inoue, Haruhisa
    PSYCHOGERIATRICS, 2012, 12 (02) : 115 - 119