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      Assembly of Functional Forebrain Spheroids from Human Pluripotent Cells

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          SUMMARY

          The development of the nervous system involves a coordinated succession of events including the migration of GABAergic neurons from ventral to dorsal forebrain and their integration into cortical circuits. However, these interregional interactions have not yet been modelled with human cells. Here, we generate from human pluripotent cells three-dimensional spheroids resembling either the dorsal or ventral forebrain and containing cortical glutamatergic or GABAergic neurons. These subdomain-specific forebrain spheroids can be assembled to recapitulate the saltatory migration of interneurons similar to migration in fetal forebrain. Using this system, we find that in Timothy syndrome– a neurodevelopmental disorder that is caused by mutations in the Ca V1.2 calcium channel, interneurons display abnormal migratory saltations. We also show that after migration, interneurons functionally integrate with glutamatergic neurons to form a microphysiological system. We anticipate that this approach will be useful for studying development and disease, and for deriving spheroids that resemble other brain regions to assemble circuits in vitro.

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          Most cited references37

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          Accounting for technical noise in single-cell RNA-seq experiments.

          Single-cell RNA-seq can yield valuable insights about the variability within a population of seemingly homogeneous cells. We developed a quantitative statistical method to distinguish true biological variability from the high levels of technical noise in single-cell experiments. Our approach quantifies the statistical significance of observed cell-to-cell variability in expression strength on a gene-by-gene basis. We validate our approach using two independent data sets from Arabidopsis thaliana and Mus musculus.
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            Interneuron dysfunction in psychiatric disorders.

            Schizophrenia, autism and intellectual disabilities are best understood as spectrums of diseases that have broad sets of causes. However, it is becoming evident that these conditions also have overlapping phenotypes and genetics, which is suggestive of common deficits. In this context, the idea that the disruption of inhibitory circuits might be responsible for some of the clinical features of these disorders is gaining support. Recent studies in animal models demonstrate that the molecular basis of such disruption is linked to specific defects in the development and function of interneurons - the cells that are responsible for establishing inhibitory circuits in the brain. These insights are leading to a better understanding of the causes of schizophrenia, autism and intellectual disabilities, and may contribute to the development of more-effective therapeutic interventions.
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              Interneuron cell types are fit to function.

              Understanding brain circuits begins with an appreciation of their component parts - the cells. Although GABAergic interneurons are a minority population within the brain, they are crucial for the control of inhibition. Determining the diversity of these interneurons has been a central goal of neurobiologists, but this amazing cell type has so far defied a generalized classification system. Interneuron complexity within the telencephalon could be simplified by viewing them as elaborations of a much more finite group of developmentally specified cardinal classes that become further specialized as they mature. Our perspective emphasizes that the ultimate goal is to dispense with classification criteria and directly define interneuron types by function.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                23 June 2017
                26 April 2017
                04 May 2017
                08 February 2018
                : 545
                : 7652
                : 54-59
                Affiliations
                [1 ]Department of Psychiatry & Behavioral Sciences, Center for Sleep Sciences and Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
                [2 ]Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA
                [3 ]Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA
                [4 ]Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA
                [5 ]BD Genomics, Menlo Park, CA 94025, USA
                [6 ]Department of Biochemistry and Biophysics, The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA 94143, USA
                [7 ]European Molecular Biology Laboratory (EMBL), Genome Biology Unit, 69117 Heidelberg, Germany
                [8 ]Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305, USA
                Author notes
                [# ]Correspondence: Sergiu P. Pașca (S.P.P.), spasca@ 123456stanford.edu
                [*]

                Equal contribution, co-first authors

                Article
                NIHMS865779
                10.1038/nature22330
                5805137
                28445465
                27915b86-b3c5-4734-b01c-8c01446baca0

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