Journal
MICROSYSTEMS & NANOENGINEERING
Volume 6, Issue 1, Pages -Publisher
SPRINGERNATURE
DOI: 10.1038/s41378-020-0165-z
Keywords
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Funding
- Strategic Priority Research Program of the Chinese Academy of Sciences [XDB32030200, XDB29050301, XDA16020900]
- National Science and Technology Major Project [2018ZX09201017-001001]
- National Key R&D Program of China [2017YFB0405400]
- National Nature Science Foundation of China [31671038, 31971373]
- Innovation Program of Science and Research from the DICP, CAS [DICP TMSR201601]
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Prenatal exposure to environmental insults can increase the risk of developing neurodevelopmental disorders. Administration of the antiepileptic drug valproic acid (VPA) during pregnancy is tightly associated with a high risk of neurological disorders in offspring. However, the lack of an ideal human model hinders our comprehensive understanding of the impact of VPA exposure on fetal brain development, especially in early gestation. Herein, we present the first report indicating the effects of VPA on brain development at early stages using engineered cortical organoids from human induced pluripotent stem cells (hiPSCs). Cortical organoids were generated on micropillar arrays in a controlled manner, recapitulating the critical features of human brain development during early gestation. With VPA exposure, cortical organoids exhibited neurodevelopmental dysfunction characterized by increased neuron progenitors, inhibited neuronal differentiation and altered forebrain regionalization. Transcriptome analysis showed new markedly altered genes (e.g., KLHL1, LHX9, and MGARP) and a large number of differential expression genes (DEGs), some of which are related to autism. In particular, comparison of transcriptome data via GSEA and correlation analysis revealed the high similarity between VPA-exposed organoids with the postmortem ASD brain and autism patient-derived organoids, implying the high risk of autism with prenatal VPA exposure, even in early gestation. These new findings facilitate a better understanding of the cellular and molecular mechanisms underlying postnatal brain disorders (such as autism) with prenatal VPA exposure. This established cortical organoid-on-a-chip platform is valuable for probing neurodevelopmental disorders under environmental exposure and can be extended to applications in the study of diseases and drug testing. Simplified brain models enable effective drug testingMiniaturized 3D models of the developing human brain provide a unique opportunity to assess the effects of a widely-used drug for neurological disorders on early-stage fetuses. Evidence suggests that valproic acid, a common treatment for epilepsy and bipolar disorder, may undermine healthy brain development in the first trimester of pregnancy. These effects have proven difficult to study, but researchers led by Jianhua Qin of the Dalian Institute of Chemical Physics have demonstrated that human cortical 'organoids' model offer valuable insights into this question. These stem cell-derived complex structures mirror key features of the fetal brain, by generating arrays of these organoids, the researchers could measure how valproic acid affects gene expression, cell growth, and maturation. They identified early signatures of abnormal development, supporting further use of this model to study the drug's impact during pregnancy.
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