Epithelial Vegfa Specifies a Distinct Endothelial Population in the Mouse Lung

The lung microvasculature is essential for gas exchange and commonly considered homogeneous. We show that VEGFA from the epithelium is required for a distinct endothelial cell (EC) population in the mouse lung. Vegfa is predominantly expressed by alveolar type 1 (AT1) cells and locally required to s...

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Published inDevelopmental cell Vol. 52; no. 5; pp. 617 - 630.e6
Main Authors Vila Ellis, Lisandra, Cain, Margo P., Hutchison, Vera, Flodby, Per, Crandall, Edward D., Borok, Zea, Zhou, Bin, Ostrin, Edwin J., Wythe, Joshua D., Chen, Jichao
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 09.03.2020
Subjects
Online AccessGet full text
ISSN1534-5807
1878-1551
1878-1551
DOI10.1016/j.devcel.2020.01.009

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Abstract The lung microvasculature is essential for gas exchange and commonly considered homogeneous. We show that VEGFA from the epithelium is required for a distinct endothelial cell (EC) population in the mouse lung. Vegfa is predominantly expressed by alveolar type 1 (AT1) cells and locally required to specify a subset of ECs. Single-cell RNA sequencing (scRNA-seq) reveals that ∼15% of lung ECs are transcriptionally distinct—marked by Carbonic anhydrase 4 (Car4)—and arise from bulk ECs, as suggested by trajectory analysis. Car4 ECs have extensive cellular projections and are separated from AT1 cells by a limited basement membrane without intervening pericytes. Car4 ECs are specifically lost upon epithelial Vegfa deletion; without Car4 ECs, the alveolar space is aberrantly enlarged despite the normal appearance of myofibroblasts. Lung Car4 ECs and retina tip ECs have common and distinct features. These findings support a signaling role of AT1 cells and shed light on alveologenesis. [Display omitted] •AT1 epithelial cells express VEGFA, which promotes local alveolar angiogenesis•scRNA-seq identifies a molecularly distinct lung EC population, labeled by CAR4•CAR4 ECs display extended morphology and are lost upon epithelial Vegfa deletion•CAR4 ECs contribute to alveolar morphogenesis independent of myofibroblasts Using imaging and single-cell RNA-seq, Vila Ellis et al. identify a lung endothelial cell (EC) population with a unique transcriptome, location, morphology, and function in lung development. These ECs are involved in alveolar morphogenesis independent of myofibroblasts.
AbstractList The lung microvasculature is essential for gas exchange and commonly considered homogeneous. We show that VEGFA from the epithelium is required for a distinct endothelial cell (EC) population in the mouse lung. Vegfa is predominantly expressed by alveolar type 1 (AT1) cells and locally required to specify a subset of ECs. Single-cell RNA sequencing (scRNA-seq) reveals that ∼15% of lung ECs are transcriptionally distinct-marked by Carbonic anhydrase 4 (Car4)-and arise from bulk ECs, as suggested by trajectory analysis. Car4 ECs have extensive cellular projections and are separated from AT1 cells by a limited basement membrane without intervening pericytes. Car4 ECs are specifically lost upon epithelial Vegfa deletion; without Car4 ECs, the alveolar space is aberrantly enlarged despite the normal appearance of myofibroblasts. Lung Car4 ECs and retina tip ECs have common and distinct features. These findings support a signaling role of AT1 cells and shed light on alveologenesis.The lung microvasculature is essential for gas exchange and commonly considered homogeneous. We show that VEGFA from the epithelium is required for a distinct endothelial cell (EC) population in the mouse lung. Vegfa is predominantly expressed by alveolar type 1 (AT1) cells and locally required to specify a subset of ECs. Single-cell RNA sequencing (scRNA-seq) reveals that ∼15% of lung ECs are transcriptionally distinct-marked by Carbonic anhydrase 4 (Car4)-and arise from bulk ECs, as suggested by trajectory analysis. Car4 ECs have extensive cellular projections and are separated from AT1 cells by a limited basement membrane without intervening pericytes. Car4 ECs are specifically lost upon epithelial Vegfa deletion; without Car4 ECs, the alveolar space is aberrantly enlarged despite the normal appearance of myofibroblasts. Lung Car4 ECs and retina tip ECs have common and distinct features. These findings support a signaling role of AT1 cells and shed light on alveologenesis.
The lung microvasculature is essential for gas exchange and commonly considered homogeneous. We show that VEGFA from the epithelium is required for a distinct endothelial cell (EC) population in the mouse lung. Vegfa is predominantly expressed by alveolar type 1 (AT1) cells and locally required to specify a subset of ECs. Single cell RNA-seq reveals that ~15% of lung ECs are transcriptionally distinct – marked by Carbonic anhydrase 4 (Car4) – and arise from bulk ECs, as suggested by trajectory analysis. Car4 ECs have extensive cellular projections and are separated from AT1 cells by a limited basement membrane without intervening pericytes. Car4 ECs are specifically lost upon epithelial Vegfa deletion; without Car4 ECs, the alveolar space is aberrantly enlarged despite the normal appearance of myofibroblasts. Lung Car4 ECs and retina tip ECs have common and distinct features. These findings support a signaling role of AT1 cells and shed light on alveologenesis. Using imaging and single cell RNA-seq, Vila Ellis et al. identify a lung endothelial cell (EC) population with a unique transcriptome, location, morphology, and function in lung development. These ECs are involved in alveolar morphogenesis independent of myofibroblasts.
The lung microvasculature is essential for gas exchange and commonly considered homogeneous. We show that VEGFA from the epithelium is required for a distinct endothelial cell (EC) population in the mouse lung. Vegfa is predominantly expressed by alveolar type 1 (AT1) cells and locally required to specify a subset of ECs. Single-cell RNA sequencing (scRNA-seq) reveals that ∼15% of lung ECs are transcriptionally distinct-marked by Carbonic anhydrase 4 (Car4)-and arise from bulk ECs, as suggested by trajectory analysis. Car4 ECs have extensive cellular projections and are separated from AT1 cells by a limited basement membrane without intervening pericytes. Car4 ECs are specifically lost upon epithelial Vegfa deletion; without Car4 ECs, the alveolar space is aberrantly enlarged despite the normal appearance of myofibroblasts. Lung Car4 ECs and retina tip ECs have common and distinct features. These findings support a signaling role of AT1 cells and shed light on alveologenesis.
The lung microvasculature is essential for gas exchange and commonly considered homogeneous. We show that VEGFA from the epithelium is required for a distinct endothelial cell (EC) population in the mouse lung. Vegfa is predominantly expressed by alveolar type 1 (AT1) cells and locally required to specify a subset of ECs. Single-cell RNA sequencing (scRNA-seq) reveals that ∼15% of lung ECs are transcriptionally distinct—marked by Carbonic anhydrase 4 (Car4)—and arise from bulk ECs, as suggested by trajectory analysis. Car4 ECs have extensive cellular projections and are separated from AT1 cells by a limited basement membrane without intervening pericytes. Car4 ECs are specifically lost upon epithelial Vegfa deletion; without Car4 ECs, the alveolar space is aberrantly enlarged despite the normal appearance of myofibroblasts. Lung Car4 ECs and retina tip ECs have common and distinct features. These findings support a signaling role of AT1 cells and shed light on alveologenesis. [Display omitted] •AT1 epithelial cells express VEGFA, which promotes local alveolar angiogenesis•scRNA-seq identifies a molecularly distinct lung EC population, labeled by CAR4•CAR4 ECs display extended morphology and are lost upon epithelial Vegfa deletion•CAR4 ECs contribute to alveolar morphogenesis independent of myofibroblasts Using imaging and single-cell RNA-seq, Vila Ellis et al. identify a lung endothelial cell (EC) population with a unique transcriptome, location, morphology, and function in lung development. These ECs are involved in alveolar morphogenesis independent of myofibroblasts.
Author Zhou, Bin
Wythe, Joshua D.
Cain, Margo P.
Ostrin, Edwin J.
Chen, Jichao
Crandall, Edward D.
Borok, Zea
Flodby, Per
Hutchison, Vera
Vila Ellis, Lisandra
AuthorAffiliation 5 Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine and Hastings Center for Pulmonary Research, University of Southern California, Los Angeles, California 90033, USA
6 The State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai, 200031, China
8 Department of Molecular Physiology and Biophysics, Cardiovascular Research Institute, Baylor College of Medicine, Houston, TX 77030, USA
3 The University of Texas MD Anderson Cancer Center UT Health Graduate School of Biomedical Sciences, Houston, Texas 77030, USA
4 Graduate Program in Developmental Biology, Baylor College of Medicine, Houston, Texas 77030, USA
2 Tecnologico de Monterrey – Escuela de Medicina, Monterrey 64710, Mexico
1 Department of Pulmonary Medicine, the University of Texas M. D. Anderson Canc
AuthorAffiliation_xml – name: 3 The University of Texas MD Anderson Cancer Center UT Health Graduate School of Biomedical Sciences, Houston, Texas 77030, USA
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  surname: Zhou
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  surname: Chen
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  email: jchen16@mdanderson.org
  organization: Department of Pulmonary Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32059772$$D View this record in MEDLINE/PubMed
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ISSN 1534-5807
1878-1551
IngestDate Thu Aug 21 18:05:58 EDT 2025
Tue Aug 05 10:15:57 EDT 2025
Wed Feb 19 02:23:55 EST 2025
Tue Jul 01 00:48:11 EDT 2025
Thu Apr 24 23:11:18 EDT 2025
Fri Feb 23 02:48:53 EST 2024
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Issue 5
Keywords angiogenesis
VEGF
endothelial cell
lung alveolar type 1 cell
single-cell RNA-seq
lung vasculature
vascular biology
lung development
alveologenesis
CAR4
Language English
License Copyright © 2020 Elsevier Inc. All rights reserved.
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content type line 23
AUTHOR CONTRIBUTIONS
LVE, JDW, and JC designed research; LVE, MPC, VH, EJO, and JC performed research; PF, EDC, and ZB provided the Aqp5Cre mice; BZ provided the AplnCreER mice; LVE, JDW, and JC wrote the paper; all authors read and approved the paper.
OpenAccessLink http://www.cell.com/article/S1534580720300101/pdf
PMID 32059772
PQID 2355964146
PQPubID 23479
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_7170573
proquest_miscellaneous_2355964146
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  year: 2020
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  day: 09
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– reference: 32155436 - Dev Cell. 2020 Mar 9;52(5):546-547
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Snippet The lung microvasculature is essential for gas exchange and commonly considered homogeneous. We show that VEGFA from the epithelium is required for a distinct...
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SubjectTerms Alveolar Epithelial Cells - cytology
Alveolar Epithelial Cells - metabolism
alveologenesis
angiogenesis
Animals
CAR4
Carbonic Anhydrase IV - genetics
Carbonic Anhydrase IV - metabolism
Cells, Cultured
endothelial cell
Endothelial Cells - cytology
Endothelial Cells - metabolism
Endothelium, Vascular - cytology
Endothelium, Vascular - metabolism
Lung - cytology
Lung - growth & development
Lung - metabolism
lung alveolar type 1 cell
lung development
lung vasculature
Mice
Morphogenesis
Myofibroblasts - cytology
Neovascularization, Physiologic
single-cell RNA-seq
vascular biology
Vascular Endothelial Growth Factor A - genetics
Vascular Endothelial Growth Factor A - metabolism
VEGF
Title Epithelial Vegfa Specifies a Distinct Endothelial Population in the Mouse Lung
URI https://dx.doi.org/10.1016/j.devcel.2020.01.009
https://www.ncbi.nlm.nih.gov/pubmed/32059772
https://www.proquest.com/docview/2355964146
https://pubmed.ncbi.nlm.nih.gov/PMC7170573
Volume 52
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