Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development
Xiaoying Fan#, Yuanyuan Fu#, Xin Zhou#, Le Sun#, Ming Yang, Mengdi Wang, Ruiguo Chen, Qian Wu, Jun Yong, Ji Dong, Lu Wen, Jie Qiao*, Xiaoqun Wang* and Fuchou Tang*
Abstract
Neurogenesis processes differ in different areas of the cortex in many species, including humans. Here, we performed single-cell transcriptome profiling of the four cortical lobes and pons during human embryonic and fetal development. We identified distinct subtypes of neural progenitor cells (NPCs) and their molecular signatures, including a group of previously unidentified transient NPCs. We specified the neurogenesis path and molecular regulations of the human deep-layer, upper-layer, and mature neurons. Neurons showed clear spatial and temporal distinctions, while glial cells of different origins showed development patterns similar to those of mice, and we captured the developmental trajectory of oligodendrocyte lineage cells until the human mid-fetal stage. Additionally, we verified region-specific characteristics of neurons in the cortex, including their distinct electrophysiological features. With systematic single-cell analysis, we decoded human neuronal development in temporal and spatial dimensions from GW7 to GW28, offering deeper insights into the molecular regulations underlying human neurogenesis and cortical development.
附件下载：
Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development, Sci Adv, 21 Aug 2020
Science Advances, 21 August, 2020, DOI：https://doi.org/10.1126/sciadv.aaz2978
Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development
Xiaoying Fan#, Yuanyuan Fu#, Xin Zhou#, Le Sun#, Ming Yang, Mengdi Wang, Ruiguo Chen, Qian Wu, Jun Yong, Ji Dong, Lu Wen, Jie Qiao*, Xiaoqun Wang* and Fuchou Tang*
Abstract
Neurogenesis processes differ in different areas of the cortex in many species, including humans. Here, we performed single-cell transcriptome profiling of the four cortical lobes and pons during human embryonic and fetal development. We identified distinct subtypes of neural progenitor cells (NPCs) and their molecular signatures, including a group of previously unidentified transient NPCs. We specified the neurogenesis path and molecular regulations of the human deep-layer, upper-layer, and mature neurons. Neurons showed clear spatial and temporal distinctions, while glial cells of different origins showed development patterns similar to those of mice, and we captured the developmental trajectory of oligodendrocyte lineage cells until the human mid-fetal stage. Additionally, we verified region-specific characteristics of neurons in the cortex, including their distinct electrophysiological features. With systematic single-cell analysis, we decoded human neuronal development in temporal and spatial dimensions from GW7 to GW28, offering deeper insights into the molecular regulations underlying human neurogenesis and cortical development.
文章链接：https://advances.sciencemag.org/content/6/34/eaaz2978
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