49
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Individual brain organoids reproducibly form cell diversity of the human cerebral cortex

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary Paragraph

          Experimental models of the human brain are needed for basic understanding of its development and disease 1 . Human brain organoids hold unprecedented promise for this purpose; however, they are plagued by high organoid-to-organoid variability 2, 3 . This has raised doubts as to whether developmental processes of the human brain can occur outside the context of embryogenesis with a degree of reproducibility comparable to the endogenous tissue. Here, we show that an organoid model of the dorsal forebrain can achieve reproducible generation of a rich diversity of cell types appropriate for the human cerebral cortex. Using single-cell RNA sequencing of 166,242 cells isolated from 21 individual organoids, we find that 95% of the organoids generate a virtually indistinguishable compendium of cell types, through the same developmental trajectories, and with organoid-to-organoid variability comparable to that of individual endogenous brains. Furthermore, organoids derived from different stem cell lines show consistent reproducibility in the cell types produced. The data demonstrate that reproducible development of complex central nervous system cellular diversity does not require the context of the embryo, and that establishment of terminal cell identity is a highly constrained process that can emerge from diverse stem cell origins and growth environments.

          Related collections

          Most cited references22

          • Record: found
          • Abstract: found
          • Article: not found

          Neuronal subtype-specific genes that control corticospinal motor neuron development in vivo.

          Within the vertebrate nervous system, the presence of many different lineages of neurons and glia complicates the molecular characterization of single neuronal populations. In order to elucidate molecular mechanisms underlying the specification and development of corticospinal motor neurons (CSMN), we purified CSMN at distinct stages of development in vivo and compared their gene expression to two other pure populations of cortical projection neurons: callosal projection neurons and corticotectal projection neurons. We found genes that are potentially instructive for CSMN development, as well as genes that are excluded from CSMN and are restricted to other populations of neurons, even within the same cortical layer. Loss-of-function experiments in null mutant mice for Ctip2 (also known as Bcl11b), one of the newly characterized genes, demonstrate that it plays a critical role in the development of CSMN axonal projections to the spinal cord in vivo, confirming that we identified central genetic determinants of the CSMN population.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Molecular identity of human outer radial glia during cortical development.

            Radial glia, the neural stem cells of the neocortex, are located in two niches: the ventricular zone and outer subventricular zone. Although outer subventricular zone radial glia may generate the majority of human cortical neurons, their molecular features remain elusive. By analyzing gene expression across single cells, we find that outer radial glia preferentially express genes related to extracellular matrix formation, migration, and stemness, including TNC, PTPRZ1, FAM107A, HOPX, and LIFR. Using dynamic imaging, immunostaining, and clonal analysis, we relate these molecular features to distinctive behaviors of outer radial glia, demonstrate the necessity of STAT3 signaling for their cell cycle progression, and establish their extensive proliferative potential. These results suggest that outer radial glia directly support the subventricular niche through local production of growth factors, potentiation of growth factor signals by extracellular matrix proteins, and activation of self-renewal pathways, thereby enabling the developmental and evolutionary expansion of the human neocortex.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Molecular logic of neocortical projection neuron specification, development and diversity.

              The sophisticated circuitry of the neocortex is assembled from a diverse repertoire of neuronal subtypes generated during development under precise molecular regulation. In recent years, several key controls over the specification and differentiation of neocortical projection neurons have been identified. This work provides substantial insight into the 'molecular logic' underlying cortical development and increasingly supports a model in which individual progenitor-stage and postmitotic regulators are embedded within highly interconnected networks that gate sequential developmental decisions. Here, we provide an integrative account of the molecular controls that direct the progressive development and delineation of subtype and area identity of neocortical projection neurons.
                Bookmark

                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                16 October 2019
                05 June 2019
                June 2019
                11 December 2019
                : 570
                : 7762
                : 523-527
                Affiliations
                [1 ]Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA
                [2 ]Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA
                [3 ]Klarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA
                [4 ]Eli and Edythe Broad CIRM Center for Regenerative Medicine and Stem Cell Research at USC, Los Angeles, CA 90033, USA
                [5 ]Howard Hughes Medical Institute, Koch Institute of Integrative Cancer Research, Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA
                Author notes

                Author Contributions: P.A. and S.V. conceived the experiments. S.V. generated all organoids. S.V., A.N., and M.R. cultured and characterized all organoids. S.V. performed scRNA-seq experiments, with help from X.A., B.P., and L.N.; A.K., S.S, and J.Z.L. performed scRNA-seq analysis and J.Z.L. and A.R. supervised their work. P.A., S.V., and A.K. wrote the manuscript with contributions from all authors. All authors read and approved the final manuscript.

                [* ]Correspondence and requests for materials should be addressed to Paola Arlotta at paola_arlotta@ 123456harvard.edu .
                Article
                NIHMS1529307
                10.1038/s41586-019-1289-x
                6906116
                31168097
                4fa69d54-231b-4780-abea-2fddcd9942e9

                Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

                Reprints and permissions information is available at www.nature.com/reprints.

                History
                Categories
                Article

                Uncategorized
                Uncategorized

                Comments

                Comment on this article