A molecular atlas of cell types and zonation in the brain vasculature
Cerebrovascular disease is the third most common cause of death in developed countries, but our understanding of the cells that compose the cerebral vasculature is limited. Here, using vascular single-cell transcriptomics, we provide molecular definitions for the principal types of blood vascular an...
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Published in | Nature (London) Vol. 554; no. 7693; pp. 475 - 480 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
22.02.2018
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Abstract | Cerebrovascular disease is the third most common cause of death in developed countries, but our understanding of the cells that compose the cerebral vasculature is limited. Here, using vascular single-cell transcriptomics, we provide molecular definitions for the principal types of blood vascular and vessel-associated cells in the adult mouse brain. We uncover the transcriptional basis of the gradual phenotypic change (zonation) along the arteriovenous axis and reveal unexpected cell type differences: a seamless continuum for endothelial cells versus a punctuated continuum for mural cells. We also provide insight into pericyte organotypicity and define a population of perivascular fibroblast-like cells that are present on all vessel types except capillaries. Our work illustrates the power of single-cell transcriptomics to decode the higher organizational principles of a tissue and may provide the initial chapter in a molecular encyclopaedia of the mammalian vasculature.
Single-cell transcriptomic analysis of the murine blood–brain barrier provides molecular definitions of the main vascular cell types, classifies perivascular cell types and sheds light on the organization of the arteriovenous axis.
Molecular map of brain vascular cells
Good vascular health is essential to proper brain function. Yet brain vascular cells have not been systematically characterized at a molecular level. Christer Betsholtz and colleagues use single-cell transcriptomics to identify the molecular profiles of the main vascular cell types in the adult mouse brain. The molecular identity and phenotype of endothelial cells change gradually along the arteriovenous axis, whereas mural cells are precisely defined either as arterial or arteriole smooth muscle cells and pericytes, or as venous smooth muscle cells. The work also provides a comprehensive molecular definition of pericytes, showing that the pericytes of one organ are highly homogeneous but quite distinct from those of a different organ. Finally, the analyses uncover a novel perivascular cell type that shares some similarities with fibroblasts and that makes up the outer layer of all brain vessels except capillaries. |
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AbstractList | Cerebrovascular disease is the third most common cause of death in developed countries, but our understanding of the cells that compose the cerebral vasculature is limited. Here, using vascular single-cell transcriptomics, we provide molecular definitions for the principal types of blood vascular and vessel-associated cells in the adult mouse brain. We uncover the transcriptional basis of the gradual phenotypic change (zonation) along the arteriovenous axis and reveal unexpected cell type differences: a seamless continuum for endothelial cells versus a punctuated continuum for mural cells. We also provide insight into pericyte organotypicity and define a population of perivascular fibroblast-like cells that are present on all vessel types except capillaries. Our work illustrates the power of single-cell transcriptomics to decode the higher organizational principles of a tissue and may provide the initial chapter in a molecular encyclopaedia of the mammalian vasculature. Cerebrovascular disease is the third most common cause of death in developed countries, but our understanding of the cells that compose the cerebral vasculature is limited. Here, using vascular single-cell transcriptomics, we provide molecular definitions for the principal types of blood vascular and vessel-associated cells in the adult mouse brain. We uncover the transcriptional basis of the gradual phenotypic change (zonation) along the arteriovenous axis and reveal unexpected cell type differences: a seamless continuum for endothelial cells versus a punctuated continuum for mural cells. We also provide insight into pericyte organotypicity and define a population of perivascular fibroblast-like cells that are present on all vessel types except capillaries. Our work illustrates the power of single-cell transcriptomics to decode the higher organizational principles of a tissue and may provide the initial chapter in a molecular encyclopaedia of the mammalian vasculature. Single-cell transcriptomic analysis of the murine blood–brain barrier provides molecular definitions of the main vascular cell types, classifies perivascular cell types and sheds light on the organization of the arteriovenous axis. Molecular map of brain vascular cells Good vascular health is essential to proper brain function. Yet brain vascular cells have not been systematically characterized at a molecular level. Christer Betsholtz and colleagues use single-cell transcriptomics to identify the molecular profiles of the main vascular cell types in the adult mouse brain. The molecular identity and phenotype of endothelial cells change gradually along the arteriovenous axis, whereas mural cells are precisely defined either as arterial or arteriole smooth muscle cells and pericytes, or as venous smooth muscle cells. The work also provides a comprehensive molecular definition of pericytes, showing that the pericytes of one organ are highly homogeneous but quite distinct from those of a different organ. Finally, the analyses uncover a novel perivascular cell type that shares some similarities with fibroblasts and that makes up the outer layer of all brain vessels except capillaries. Cerebrovascular disease is the third most common cause of death in developed countries, but our understanding of the cells that compose the cerebral vasculature is limited. Here, using vascular single-cell transcriptomics, we provide molecular definitions for the principal types of blood vascular and vessel-associated cells in the adult mouse brain. We uncover the transcriptional basis of the gradual phenotypic change (zonation) along the arteriovenous axis and reveal unexpected cell type differences: a seamless continuum for endothelial cells versus a punctuated continuum for mural cells. We also provide insight into pericyte organotypicity and define a population of perivascular fibroblast-like cells that are present on all vessel types except capillaries. Our work illustrates the power of single-cell transcriptomics to decode the higher organizational principles of a tissue and may provide the initial chapter in a molecular encyclopaedia of the mammalian vasculature.Cerebrovascular disease is the third most common cause of death in developed countries, but our understanding of the cells that compose the cerebral vasculature is limited. Here, using vascular single-cell transcriptomics, we provide molecular definitions for the principal types of blood vascular and vessel-associated cells in the adult mouse brain. We uncover the transcriptional basis of the gradual phenotypic change (zonation) along the arteriovenous axis and reveal unexpected cell type differences: a seamless continuum for endothelial cells versus a punctuated continuum for mural cells. We also provide insight into pericyte organotypicity and define a population of perivascular fibroblast-like cells that are present on all vessel types except capillaries. Our work illustrates the power of single-cell transcriptomics to decode the higher organizational principles of a tissue and may provide the initial chapter in a molecular encyclopaedia of the mammalian vasculature. |
Audience | Academic |
Author | Sun, Ying Mochizuki, Naoki Zarb, Yvette Andrae, Johanna Räsänen, Markus Del Gaudio, Francesca Keller, Annika Lendahl, Urban Laviña, Bàrbara Betsholtz, Christer Raschperger, Elisabeth Vanlandewijck, Michael Mäe, Maarja Andaloussi Gouveia, Leonor Ando, Koji Lebouvier, Thibaud He, Liqun Nahar, Khayrun |
Author_xml | – sequence: 1 givenname: Michael surname: Vanlandewijck fullname: Vanlandewijck, Michael organization: Karolinska Institutet/AstraZeneca Integrated Cardio Metabolic Centre (KI/AZ ICMC), Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University – sequence: 2 givenname: Liqun surname: He fullname: He, Liqun organization: Department of Neurosurgery, Tianjin Medical University General Hospital, Tianjin Neurological Institute, Key Laboratory of Post-Neuroinjury Neuro-Repair and Regeneration in Central Nervous System, Ministry of Education and Tianjin City – sequence: 3 givenname: Maarja Andaloussi surname: Mäe fullname: Mäe, Maarja Andaloussi organization: Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University – sequence: 4 givenname: Johanna surname: Andrae fullname: Andrae, Johanna organization: Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University – sequence: 5 givenname: Koji surname: Ando fullname: Ando, Koji organization: Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University – sequence: 6 givenname: Francesca surname: Del Gaudio fullname: Del Gaudio, Francesca organization: Department of Cell and Molecular Biology, Karolinska Institutet – sequence: 7 givenname: Khayrun surname: Nahar fullname: Nahar, Khayrun organization: Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University – sequence: 8 givenname: Thibaud surname: Lebouvier fullname: Lebouvier, Thibaud organization: Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Inserm U1171, University of Lille, CHU, Memory Center, Distalz – sequence: 9 givenname: Bàrbara surname: Laviña fullname: Laviña, Bàrbara organization: Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University – sequence: 10 givenname: Leonor surname: Gouveia fullname: Gouveia, Leonor organization: Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University – sequence: 11 givenname: Ying surname: Sun fullname: Sun, Ying organization: Department of Bioinformatics, Zhongyuan Union Genetic Technology Co., Ltd., No.45 – sequence: 12 givenname: Elisabeth surname: Raschperger fullname: Raschperger, Elisabeth organization: Karolinska Institutet/AstraZeneca Integrated Cardio Metabolic Centre (KI/AZ ICMC) – sequence: 13 givenname: Markus surname: Räsänen fullname: Räsänen, Markus organization: Wihuri Research Institute and Translational Cancer Biology Program, Biomedicum Helsinki, University of Helsinki – sequence: 14 givenname: Yvette surname: Zarb fullname: Zarb, Yvette organization: Division of Neurosurgery, Zürich University Hospital, Zürich University – sequence: 15 givenname: Naoki surname: Mochizuki fullname: Mochizuki, Naoki organization: Department of Cell Biology, National Cerebral and Cardiovascular Center Research Institute, AMED-CREST, National Cerebral and Cardiovascular Center – sequence: 16 givenname: Annika surname: Keller fullname: Keller, Annika organization: Division of Neurosurgery, Zürich University Hospital, Zürich University – sequence: 17 givenname: Urban surname: Lendahl fullname: Lendahl, Urban organization: Department of Cell and Molecular Biology, Karolinska Institutet – sequence: 18 givenname: Christer surname: Betsholtz fullname: Betsholtz, Christer email: christer.betsholtz@ki.se organization: Karolinska Institutet/AstraZeneca Integrated Cardio Metabolic Centre (KI/AZ ICMC), Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29443965$$D View this record in MEDLINE/PubMed https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-349342$$DView record from Swedish Publication Index http://kipublications.ki.se/Default.aspx?queryparsed=id:137714465$$DView record from Swedish Publication Index |
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Snippet | Cerebrovascular disease is the third most common cause of death in developed countries, but our understanding of the cells that compose the cerebral... |
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Title | A molecular atlas of cell types and zonation in the brain vasculature |
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