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Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development
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)...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450478/ https://www.ncbi.nlm.nih.gov/pubmed/32923614 http://dx.doi.org/10.1126/sciadv.aaz2978 |
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author | Fan, Xiaoying Fu, Yuanyuan Zhou, Xin Sun, Le Yang, Ming Wang, Mengdi Chen, Ruiguo Wu, Qian Yong, Jun Dong, Ji Wen, Lu Qiao, Jie Wang, Xiaoqun Tang, Fuchou |
author_facet | Fan, Xiaoying Fu, Yuanyuan Zhou, Xin Sun, Le Yang, Ming Wang, Mengdi Chen, Ruiguo Wu, Qian Yong, Jun Dong, Ji Wen, Lu Qiao, Jie Wang, Xiaoqun Tang, Fuchou |
author_sort | Fan, Xiaoying |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7450478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74504782020-09-11 Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development Fan, Xiaoying Fu, Yuanyuan Zhou, Xin Sun, Le Yang, Ming Wang, Mengdi Chen, Ruiguo Wu, Qian Yong, Jun Dong, Ji Wen, Lu Qiao, Jie Wang, Xiaoqun Tang, Fuchou Sci Adv Research Articles 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. American Association for the Advancement of Science 2020-08-21 /pmc/articles/PMC7450478/ /pubmed/32923614 http://dx.doi.org/10.1126/sciadv.aaz2978 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Fan, Xiaoying Fu, Yuanyuan Zhou, Xin Sun, Le Yang, Ming Wang, Mengdi Chen, Ruiguo Wu, Qian Yong, Jun Dong, Ji Wen, Lu Qiao, Jie Wang, Xiaoqun Tang, Fuchou Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development |
title | Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development |
title_full | Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development |
title_fullStr | Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development |
title_full_unstemmed | Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development |
title_short | Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development |
title_sort | single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450478/ https://www.ncbi.nlm.nih.gov/pubmed/32923614 http://dx.doi.org/10.1126/sciadv.aaz2978 |
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