Motor neuron-derived induced pluripotent stem cells as a drug screening platform for amyotrophic lateral sclerosis

被引:3
|
作者
Amoros, Mariana A. [1 ]
Choi, Esther S. [2 ]
Cofre, Axel R. [1 ]
Dokholyan, Nikolay, V [2 ,3 ]
Duzzioni, Marcelo [1 ]
机构
[1] Univ Fed Alagoas, Inst Biol Sci & Hlth, Lab Pharmacol Innovat, Maceio, Alagoas, Brazil
[2] Penn State Coll Med, Dept Pharmacol, Hershey, PA USA
[3] Penn State Coll Med, Dept Biochem & Mol Biol, Hershey, PA USA
关键词
amyotrophic lateral sclerosis (ALS); induced pluripotent stem cells (iPSCs); drug screening; in vitro disease model; 3D cell culture; bioinformactics; motor neuron; differentiation; HUMAN SOMATIC-CELLS; CEREBRAL ORGANOIDS; HUMAN FIBROBLASTS; IPS CELLS; DIRECTED DIFFERENTIATION; MITOCHONDRIAL-FUNCTION; MOLECULAR-BIOLOGY; OXIDATIVE STRESS; SENDAI-VIRUS; SPORADIC ALS;
D O I
10.3389/fcell.2022.962881
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The development of cell culture models that recapitulate the etiology and features of nervous system diseases is central to the discovery of new drugs and their translation onto therapies. Neuronal tissues are inaccessible due to skeletal constraints and the invasiveness of the procedure to obtain them. Thus, the emergence of induced pluripotent stem cell (iPSC) technology offers the opportunity to model different neuronal pathologies. Our focus centers on iPSCs derived from amyotrophic lateral sclerosis (ALS) patients, whose pathology remains in urgent need of new drugs and treatment. In this sense, we aim to revise the process to obtain motor neurons derived iPSCs (iPSC-MNs) from patients with ALS as a drug screening model, review current 3D-models and offer a perspective on bioinformatics as a powerful tool that can aid in the progress of finding new pharmacological treatments.
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页数:19
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