Using induced pluripotent stem cells derived neurons to model brain diseases

被引:28
|
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] Parasympathetic neurons derived from human pluripotent stem cells model human diseases and development
    Wu, Hsueh-Fu
    Saito-Diaz, Kenyi
    Huang, Chia-Wei
    McAlpine, Jessica L.
    Seo, Dong Eun
    Magruder, D. Sumner
    Ishan, Mohamed
    Bergeron, Harrison C.
    Delaney, William H.
    Santori, Fabio R.
    Krishnaswamy, Smita
    Hart, Gerald W.
    Chen, Ya-Wen
    Hogan, Robert J.
    Liu, Hong-Xiang
    Ivanova, Natalia B.
    Zeltner, Nadja
    CELL STEM CELL, 2024, 31 (05) : 734 - 753.e8
  • [3] 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
  • [4] Induced Pluripotent Stem Cells to Model Blood Diseases
    Papapetrou, Eirini P.
    BLOOD, 2018, 132
  • [5] Modeling neurological diseases using patient-derived induced pluripotent stem cells
    Juopperi, Tarja A.
    Song, Hongjun
    Ming, Guo-li
    FUTURE NEUROLOGY, 2011, 6 (03) : 363 - 373
  • [6] An isogenic blood-brain barrier model comprising brain endothelial cells, astrocytes, and neurons derived from human induced pluripotent stem cells
    Canfield, Scott G.
    Stebbins, Matthew J.
    Morales, Bethsymarie Soto
    Asai, Shusaku W.
    Vatine, Gad D.
    Svendsen, Clive N.
    Palecek, Sean P.
    Shusta, Eric V.
    JOURNAL OF NEUROCHEMISTRY, 2017, 140 (06) : 874 - 888
  • [7] High content screening of induced pluripotent stem cells as a model to study human brain diseases
    Daniel Rodrigues Furtado
    BMC Proceedings, 8 (Suppl 4)
  • [8] Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells
    Hayashi, Yohei
    Takami, Miho
    Matsuo-Takasaki, Mami
    FRONTIERS IN CELLULAR NEUROSCIENCE, 2020, 14
  • [9] Establishment and characterization of human pluripotent stem cells-derived brain organoids to model cerebellar diseases
    João Brás
    Daniel Henriques
    Ricardo Moreira
    Magda M. Santana
    Rita Silva-Pedrosa
    Diana Adão
    Sandra Braz
    Ana Rita Álvaro
    Luís Pereira de Almeida
    Liliana S. Mendonça
    Scientific Reports, 12
  • [10] Establishment and characterization of human pluripotent stem cells-derived brain organoids to model cerebellar diseases
    Bras, Joao
    Henriques, Daniel
    Moreira, Ricardo
    Santana, Magda M.
    Silva-Pedrosa, Rita
    Adao, Diana
    Braz, Sandra
    Alvaro, Ana Rita
    de Almeida, Luis Pereira
    Mendonca, Liliana S.
    SCIENTIFIC REPORTS, 2022, 12 (01)