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 in | Developmental cell Vol. 52; no. 5; pp. 617 - 630.e6 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
09.03.2020
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Subjects | |
Online Access | Get full text |
ISSN | 1534-5807 1878-1551 1878-1551 |
DOI | 10.1016/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. |
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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 – name: 8 Department of Molecular Physiology and Biophysics, Cardiovascular Research Institute, Baylor College of Medicine, Houston, TX 77030, USA – name: 7 Department of General Internal Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA – name: 2 Tecnologico de Monterrey – Escuela de Medicina, Monterrey 64710, Mexico – name: 4 Graduate Program in Developmental Biology, Baylor College of Medicine, Houston, Texas 77030, USA – name: 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 – name: 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 – name: 1 Department of Pulmonary Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA |
Author_xml | – sequence: 1 givenname: Lisandra surname: Vila Ellis fullname: Vila Ellis, Lisandra organization: Department of Pulmonary Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA – sequence: 2 givenname: Margo P. surname: Cain fullname: Cain, Margo P. organization: Department of Pulmonary Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA – sequence: 3 givenname: Vera surname: Hutchison fullname: Hutchison, Vera organization: Department of Pulmonary Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA – sequence: 4 givenname: Per surname: Flodby fullname: Flodby, Per organization: Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine and Hastings Center for Pulmonary Research, University of Southern California, Los Angeles, CA 90033, USA – sequence: 5 givenname: Edward D. surname: Crandall fullname: Crandall, Edward D. organization: Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine and Hastings Center for Pulmonary Research, University of Southern California, Los Angeles, CA 90033, USA – sequence: 6 givenname: Zea surname: Borok fullname: Borok, Zea organization: Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine and Hastings Center for Pulmonary Research, University of Southern California, Los Angeles, CA 90033, USA – sequence: 7 givenname: Bin surname: Zhou fullname: Zhou, Bin organization: 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 – sequence: 8 givenname: Edwin J. surname: Ostrin fullname: Ostrin, Edwin J. organization: Department of Pulmonary Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA – sequence: 9 givenname: Joshua D. surname: Wythe fullname: Wythe, Joshua D. organization: Department of Molecular Physiology and Biophysics, Cardiovascular Research Institute, Baylor College of Medicine, Houston, TX 77030, USA – sequence: 10 givenname: Jichao surname: Chen fullname: Chen, Jichao email: jchen16@mdanderson.org organization: Department of Pulmonary Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA |
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Keywords | angiogenesis VEGF endothelial cell lung alveolar type 1 cell single-cell RNA-seq lung vasculature vascular biology lung development alveologenesis CAR4 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 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. |
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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 |
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