| Literature DB >> 27118425 |
Xuyu Qian1, Ha Nam Nguyen2, Mingxi M Song3, Christopher Hadiono4, Sarah C Ogden5, Christy Hammack5, Bing Yao6, Gregory R Hamersky7, Fadi Jacob8, Chun Zhong9, Ki-Jun Yoon9, William Jeang10, Li Lin6, Yujing Li6, Jai Thakor8, Daniel A Berg8, Ce Zhang9, Eunchai Kang9, Michael Chickering8, David Nauen11, Cheng-Ying Ho12, Zhexing Wen9, Kimberly M Christian9, Pei-Yong Shi13, Brady J Maher14, Hao Wu15, Peng Jin6, Hengli Tang5, Hongjun Song16, Guo-Li Ming17.
Abstract
Cerebral organoids, three-dimensional cultures that model organogenesis, provide a new platform to investigate human brain development. High cost, variability, and tissue heterogeneity limit their broad applications. Here, we developed a miniaturized spinning bioreactor (SpinΩ) to generate forebrain-specific organoids from human iPSCs. These organoids recapitulate key features of human cortical development, including progenitor zone organization, neurogenesis, gene expression, and, notably, a distinct human-specific outer radial glia cell layer. We also developed protocols for midbrain and hypothalamic organoids. Finally, we employed the forebrain organoid platform to model Zika virus (ZIKV) exposure. Quantitative analyses revealed preferential, productive infection of neural progenitors with either African or Asian ZIKV strains. ZIKV infection leads to increased cell death and reduced proliferation, resulting in decreased neuronal cell-layer volume resembling microcephaly. Together, our brain-region-specific organoids and SpinΩ provide an accessible and versatile platform for modeling human brain development and disease and for compound testing, including potential ZIKV antiviral drugs.Entities:
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Year: 2016 PMID: 27118425 PMCID: PMC4900885 DOI: 10.1016/j.cell.2016.04.032
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582