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Pulmonary pericytes regulate lung morphogenesis.
Kato, Katsuhiro; Diéguez-Hurtado, Rodrigo; Park, Do Young; Hong, Seon Pyo; Kato-Azuma, Sakiko; Adams, Susanne; Stehling, Martin; Trappmann, Britta; Wrana, Jeffrey L; Koh, Gou Young; Adams, Ralf H.
Affiliation
  • Kato K; Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, and University of Münster, Faculty of Medicine, D-48149, Münster, Germany. katsuhiro.kato@mpi-muenster.mpg.de.
  • Diéguez-Hurtado R; Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, and University of Münster, Faculty of Medicine, D-48149, Münster, Germany.
  • Park DY; Center for Vascular Research, Institute of Basic Science (IBS), Daejeon, 34141, Republic of Korea.
  • Hong SP; Graduate School of Medical Science and Engineering, and Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Korea.
  • Kato-Azuma S; Center for Vascular Research, Institute of Basic Science (IBS), Daejeon, 34141, Republic of Korea.
  • Adams S; Graduate School of Medical Science and Engineering, and Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Korea.
  • Stehling M; Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, and University of Münster, Faculty of Medicine, D-48149, Münster, Germany.
  • Trappmann B; Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, and University of Münster, Faculty of Medicine, D-48149, Münster, Germany.
  • Wrana JL; Electron Microscopy and Flow Cytometry Units, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.
  • Koh GY; Bioactive Materials Laboratory, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.
  • Adams RH; Centre for Systems Biology, Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, M5G 1X5, Canada.
Nat Commun ; 9(1): 2448, 2018 06 22.
Article in En | MEDLINE | ID: mdl-29934496
Blood vessels are essential for blood circulation but also control organ growth, homeostasis, and regeneration, which has been attributed to the release of paracrine signals by endothelial cells. Endothelial tubules are associated with specialised mesenchymal cells, termed pericytes, which help to maintain vessel wall integrity. Here we identify pericytes as regulators of epithelial and endothelial morphogenesis in postnatal lung. Mice lacking expression of the Hippo pathway components YAP and TAZ in pericytes show defective alveologenesis. Mutant pericytes are present in normal numbers but display strongly reduced expression of hepatocyte growth factor leading to impaired activation of the c-Met receptor, which is expressed by alveolar epithelial cells. YAP and TAZ are also required for expression of angiopoietin-1 by pulmonary pericytes, which also controls hepatocyte growth factor expression and thereby alveologenesis in an autocrine fashion. These findings establish that pericytes have important, organ-specific signalling properties and coordinate the behavior of epithelial and vascular cells during lung morphogenesis.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pulmonary Alveoli / Neovascularization, Physiologic / Pericytes / Morphogenesis Type of study: Prognostic_studies Limits: Animals Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2018 Document type: Article Affiliation country: Germany Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pulmonary Alveoli / Neovascularization, Physiologic / Pericytes / Morphogenesis Type of study: Prognostic_studies Limits: Animals Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2018 Document type: Article Affiliation country: Germany Country of publication: United kingdom