A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain

被引:181
作者
Yao, Zizhen [1 ]
van Velthoven, Cindy T. J. [1 ]
Kunst, Michael [1 ]
Zhang, Meng [2 ]
Mcmillen, Delissa [1 ]
Lee, Changkyu [1 ]
Jung, Won [2 ]
Goldy, Jeff [1 ]
Abdelhak, Aliya [1 ]
Aitken, Matthew [1 ]
Baker, Katherine [1 ]
Baker, Pamela [1 ]
Barkan, Eliza [1 ]
Bertagnolli, Darren [1 ]
Bhandiwad, Ashwin [1 ]
Bielstein, Cameron [1 ]
Bishwakarma, Prajal [1 ]
Campos, Jazmin [1 ]
Carey, Daniel [1 ]
Casper, Tamara [1 ]
Chakka, Anish Bhaswanth [1 ]
Chakrabarty, Rushil [1 ]
Chavan, Sakshi [1 ]
Chen, Min [3 ]
Clark, Michael [1 ]
Close, Jennie [1 ]
Crichton, Kirsten [1 ]
Daniel, Scott [1 ]
Divalentin, Peter [1 ]
Dolbeare, Tim [1 ]
Ellingwood, Lauren [1 ]
Fiabane, Elysha [1 ]
Fliss, Timothy [1 ]
Gee, James [3 ]
Gerstenberger, James [1 ]
Glandon, Alexandra [1 ]
Gloe, Jessica [1 ]
Gould, Joshua [4 ]
Gray, James [1 ]
Guilford, Nathan [1 ]
Guzman, Junitta [1 ]
Hirschstein, Daniel [1 ]
Ho, Windy [1 ]
Hooper, Marcus [1 ]
Huang, Mike [1 ]
Hupp, Madie [1 ]
Jin, Kelly [1 ]
Kroll, Matthew [1 ]
Lathia, Kanan [1 ]
Leon, Arielle [1 ]
机构
[1] Allen Inst Brain Sci, Seattle, WA USA
[2] Harvard Univ, Howard Hughes Med Inst, Dept Chem & Chem Biol, Dept Phys, Cambridge, MA 02138 USA
[3] Univ Penn, Philadelphia, PA USA
[4] Proneurotech, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
NEURAL STEM-CELLS; CIRCUMVENTRICULAR ORGANS; RESOLVED TRANSCRIPTOMICS; RNA-SEQ; NEURONS; EXPRESSION; IDENTITY; CLASSIFICATION; MIGRATION; FAMILY;
D O I
10.1038/s41586-023-06812-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mammalian brain consists of millions to billions of cells that are organized into many cell types with specific spatial distribution patterns and structural and functional properties(1-3). Here we report a comprehensive and high-resolution transcriptomic and spatial cell-type atlas for the whole adult mouse brain. The cell-type atlas was created by combining a single-cell RNA-sequencing (scRNA-seq) dataset of around 7 million cells profiled (approximately 4.0 million cells passing quality control), and a spatial transcriptomic dataset of approximately 4.3 million cells using multiplexed error-robust fluorescence in situ hybridization (MERFISH). The atlas is hierarchically organized into 4 nested levels of classification: 34 classes, 338 subclasses, 1,201 supertypes and 5,322 clusters. We present an online platform, Allen Brain Cell Atlas, to visualize the mouse whole-brain cell-type atlas along with the single-cell RNA-sequencing and MERFISH datasets. We systematically analysed the neuronal and non-neuronal cell types across the brain and identified a high degree of correspondence between transcriptomic identity and spatial specificity for each cell type. The results reveal unique features of cell-type organization in different brain regions-in particular, a dichotomy between the dorsal and ventral parts of the brain. The dorsal part contains relatively fewer yet highly divergent neuronal types, whereas the ventral part contains more numerous neuronal types that are more closely related to each other. Our study also uncovered extraordinary diversity and heterogeneity in neurotransmitter and neuropeptide expression and co-expression patterns in different cell types. Finally, we found that transcription factors are major determinants of cell-type classification and identified a combinatorial transcription factor code that defines cell types across all parts of the brain. The whole mouse brain transcriptomic and spatial cell-type atlas establishes a benchmark reference atlas and a foundational resource for integrative investigations of cellular and circuit function, development and evolution of the mammalian brain.
引用
收藏
页码:317 / 332
页数:52
相关论文
共 143 条
  • [1] New Insights Into Cholinergic Neuron Diversity
    Ahmed, Noorya Yasmin
    Knowles, Rhys
    Dehorter, Nathalie
    [J]. FRONTIERS IN MOLECULAR NEUROSCIENCE, 2019, 12
  • [2] Developmental specification of forebrain cholinergic neurons
    Allaway, Kathryn C.
    Machold, Robert
    [J]. DEVELOPMENTAL BIOLOGY, 2017, 421 (01) : 1 - 7
  • [3] Allen Institute for Brain Science, 2023, 10x Multiome sample processing. Protocols.io, DOI [10.17504/protocols.io.bp2l61mqrvqe/v1, DOI 10.17504/PROTOCOLS.IO.BP2L61MQRVQE/V1]
  • [4] Allen Institute for Brain Science, 2023, RAISINs (RNA-seq for profiling intact nuclei with ribosome-bound mRNA) nuclei isolation from mouse CNS tissue protocol. Protocols.io, DOI [10.17504/protocols.io.4r3l22n5pl1y/v1, DOI 10.17504/PROTOCOLS.IO.4R3L22N5PL1Y/V1]
  • [5] Allen Institute for Brain Science, 2021, 10Xv2 RNASeq sample processing. Protocols.io, DOI [10.17504/protocols.io.bq68mzhw, DOI 10.17504/PROTOCOLS.IO.BQ68MZHW]
  • [6] Allen Institute for Brain Science, 2020, FACS single cell sorting V.4, DOI [10.17504/protocols.io.be4cjgsw, DOI 10.17504/PROTOCOLS.IO.BE4CJGSW]
  • [7] Allen Institute for Brain Science, 2022, Mouse whole cell tissue processing for 10x Genomics Platform V.9. Protocols.io, DOI [10.17504/protocols.io.q26g7b52klwz/v9, DOI 10.17504/PROTOCOLS.IO.Q26G7B52KLWZ/V9]
  • [8] Allen Institute for Brain Science, 2022, 10Xv3.1 Genomics sample processing V.2. Protocols.io, DOI [10.17504/protocols.io.dm6gpwd8jlzp/v2, DOI 10.17504/PROTOCOLS.IO.DM6GPWD8JLZP/V2]
  • [9] Allen Institute for Brain Science, 2023, Mouse brain perfusion and flash freezing. Protocols.io, DOI [10.17504/protocols.io.j8nlkodr6v5r/v1, DOI 10.17504/PROTOCOLS.IO.J8NLKODR6V5R/V1]
  • [10] Allen Institute for Brain Science, 2023, HEPES-sucrose cutting solution, DOI [10.17504/protocols.io.5jyl8peq8g2w/v1, DOI 10.17504/PROTOCOLS.IO.5JYL8PEQ8G2W/V1]