Commentary: A community-based transcriptomics classification and nomenclature of neocortical cell types

Rafael Yuste, Michael Hawrylycz, Nadia Aalling, Argel Aguilar-Valles, Detlev Arendt, Ruben Armananzas, Giorgio Ascoli, Concha Bielza, Vahid Bokharaie, Tobias Borgtoft Bergmann, Irina Bystron, Marco Capogna, Yoonjeung Chang, Ann Clemens, Chris de Kock, Javier DeFelipe, Sandra Esmeralda Dos Santos, Keagan Dunville, Dirk Feldmeyer, Richard FiathGordon James Fishell, Angelica Foggetti, Xuefan Gao, Parviz Ghaderi, Natalia Goriounova, Onuyr Guentuerkuen, Kenta Hagihara, Vanessa Jane Hall, Moritz Helmstaedter, Suzana Herculano, Markus M Hilscher, Hajime Hirase, Jens Hjerling-Leffler, Rebecca Hodge, Josh Huang, Rafiq Huda, Konstantin Khodosevich, Ole Kiehn, Henner Koch, Eric S Kuebler, Malte Kuhnemund, Pedro Larranaga, Boudewijn Lelieveldt, Emma Louise Louth, Jan Hsi Lui, Huib D Mansvelder, Oscar Marin Parra, Julio Martinez, Homeira Moradi, Alok Nath, Maiken Nedergaard, Pavel Nemec, Netanel Ofer, Ulrich Gottfried Pfisterer, Samuel Pontes, William Redmond, Jean Rossier, Joshua Sanes, Richard Scheuermann, Esther Serrano-Saiz, Jochen Steiger, Peter Somogyi, Gabor Tamas, Andreas Savas Tolias, Maria Tosches, Miguel Turrero Garcia, Hermany Munguba Vieira, Christian Wozny, Thomas V Wuttke, Liu Yong, Juan Yuan, Hongkui Zeng, Ed Lein

Research output: Contribution to journalComment/debatepeer-review

Abstract / Description of output

To understand the function of cortical circuits, it is necessary to catalog their cellular diversity. Past attempts to do so using anatomical, physiological or molecular features of cortical cells have not resulted in a unified taxonomy of neuronal or glial cell types, partly due to limited data. Single-cell transcriptomics is enabling, for the first time, systematic high-throughput measurements of cortical cells and generation of datasets that hold the promise of being complete, accurate and permanent. Statistical analyses of these data reveal clusters that often correspond to cell types previously defined by morphological or physiological criteria and that appear conserved across cortical areas and species. To capitalize on these new methods, we propose the adoption of a transcriptome-based taxonomy of cell types for mammalian neocortex. This classification should be hierarchical and use a standardized nomenclature. It should be based on a probabilistic definition of a cell type and incorporate data from different approaches, developmental stages and species. A community-based classification and data aggregation model, such as a knowledge graph, could provide a common foundation for the study of cortical circuits. This community-based classification, nomenclature and data aggregation could serve as an example for cell type atlases in other parts of the body.
Original languageEnglish
Pages (from-to)1456–1468
Number of pages13
JournalNature Neuroscience
Volume23
Early online date24 Aug 2020
DOIs
Publication statusPublished - Dec 2020

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