Harnessing the potential of human induced pluripotent stem cells, functional assays and machine learning for neurodevelopmental disorders

被引:0
作者
Yang, Ziqin [1 ,2 ]
Teaney, Nicole A. [1 ,2 ]
Buttermore, Elizabeth D. [1 ,2 ,3 ]
Sahin, Mustafa [1 ,2 ,3 ]
Afshar-Saber, Wardiya [1 ,2 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Rosamund Stone Zander Translat Neurosci Ctr, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston Childrens Hosp, FM Kirby Neurobiol Ctr, Dept Neurol, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Human Neuron Core, Boston, MA USA
基金
美国国家卫生研究院;
关键词
hiPSC; neurodevelopmental disorders; patch clamping; MEA; voltage imaging; calcium imaging; machine learning; translational research; IN-VITRO; PATCH-CLAMP; CEREBRAL ORGANOIDS; CALCIUM INDICATORS; CORTICAL-NEURONS; HIGH-THROUGHPUT; NEURAL ACTIVITY; NERVOUS-SYSTEM; LARGE-SCALE; IPS CELLS;
D O I
10.3389/fnins.2024.1524577
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurodevelopmental disorders (NDDs) affect 4.7% of the global population and are associated with delays in brain development and a spectrum of impairments that can lead to lifelong disability and even mortality. Identification of biomarkers for accurate diagnosis and medications for effective treatment are lacking, in part due to the historical use of preclinical model systems that do not translate well to the clinic for neurological disorders, such as rodents and heterologous cell lines. Human-induced pluripotent stem cells (hiPSCs) are a promising in vitro system for modeling NDDs, providing opportunities to understand mechanisms driving NDDs in human neurons. Functional assays, including patch clamping, multielectrode array, and imaging-based assays, are popular tools employed with hiPSC disease models for disease investigation. Recent progress in machine learning (ML) algorithms also presents unprecedented opportunities to advance the NDD research process. In this review, we compare two-dimensional and three-dimensional hiPSC formats for disease modeling, discuss the applications of functional assays, and offer insights on incorporating ML into hiPSC-based NDD research and drug screening.
引用
收藏
页数:33
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