| Literature DB >> 27498872 |
Alfred Xuyang Sun1, Qiang Yuan2, Shawn Tan2, Yixin Xiao3, Danlei Wang3, Audrey Tze Ting Khoo3, Levena Sani4, Hoang-Dai Tran5, Paul Kim3, Yong Seng Chiew3, Kea Joo Lee6, Yi-Chun Yen3, Huck Hui Ng7, Bing Lim4, Hyunsoo Shawn Je8.
Abstract
Gamma-aminobutyric acid (GABA)-releasing interneurons play an important modulatory role in the cortex and have been implicated in multiple neurological disorders. Patient-derived interneurons could provide a foundation for studying the pathogenesis of these diseases as well as for identifying potential therapeutic targets. Here, we identified a set of genetic factors that could robustly induce human pluripotent stem cells (hPSCs) into GABAergic neurons (iGNs) with high efficiency. We demonstrated that the human iGNs express neurochemical markers and exhibit mature electrophysiological properties within 6-8 weeks. Furthermore, in vitro, iGNs could form functional synapses with other iGNs or with human-induced glutamatergic neurons (iENs). Upon transplantation into immunodeficient mice, human iGNs underwent synaptic maturation and integration into host neural circuits. Taken together, our rapid and highly efficient single-step protocol to generate iGNs may be useful to both mechanistic and translational studies of human interneurons.Entities:
Keywords: GABA; direct conversion; human pluripotent stem cells; interneuron; synapse
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Year: 2016 PMID: 27498872 DOI: 10.1016/j.celrep.2016.07.035
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423