Laryngotracheal Groove

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David Warburton - One of the best experts on this subject based on the ideXlab platform.

  • Overview of Lung Development in the Newborn Human.
    Neonatology, 2017
    Co-Authors: David Warburton
    Abstract:

    In human neonates rapid adaptation from an aqueous intrauterine environment to permanent air breathing is the rate-limiting step for extrauterine life, failure of which justifies the existence of neonatal intensive care units. The lung develops at about 4-6 weeks' gestation in humans as a ventral outpouching of the primitive foregut into the surrounding ventral mesenchyme, termed the Laryngotracheal Groove. At its posterior end lie progenitor cells that form a pair of bronchial tubes, from which arise all the distal epithelial structures of the lung. In humans, formation of the distal gas exchange surfaces begins in utero at about 20 weeks' gestation and is substantially established by term. Stereotypic branching of the proximal airway ends relatively early at 16-18 weeks at the bronchoalveolar duct junctions. Distally, about 5 finger-like alveolar ducts arise from each bronchoalveolar duct junction and ramify outwards towards the pleura. The majority of alveolar air sacs arise from the sides of the alveolar ducts and each of these alveoli can have up to 5 daughter alveoli arising from the outer surface as subsequent buds. At the end of each alveolar duct lie the mouths of 5 interconnected alveoli. Each family of alveoli arising from each bronchoalveolar duct junction has a different shape depending upon the limitations imposed by the pleural surface as well as the interstitial fascial planes.

  • Molecular Mechanisms of Early Lung Specification and Branching Morphogenesis
    Pediatric Research, 2005
    Co-Authors: David Warburton, Denise Tefft, Stijn De Langhe, Pierre-marie Del Moral, Mathieu Unbekandt, Vincent Fleury, Saverio Bellusci, Arnaud Mailleux, Kasper Wang
    Abstract:

    The “hard wiring” encoded within the genome that determines the emergence of the Laryngotracheal Groove and subsequently early lung branching morphogenesis is mediated by finely regulated, interactive growth factor signaling mechanisms that determine the automaticity of branching, interbranch length, stereotypy of branching, left-right asymmetry, and finally gas diffusion surface area. The extracellular matrix is an important regulator as well as a target for growth factor signaling in lung branching morphogenesis and alveolarization. Coordination not only of epithelial but also endothelial branching morphogenesis determines bronchial branching and the eventual alveolar-capillary interface. Improved prospects for lung protection, repair, regeneration, and engineering will depend on more detailed understanding of these processes. Herein, we concisely review the functionally integrated morphogenetic signaling network comprising the critical bone morphogenetic protein, fibroblast growth factor, Sonic hedgehog, transforming growth factor-β, vascular endothelial growth factor, and Wnt signaling pathways that specify and drive early embryonic lung morphogenesis.

  • Molecular mechanisms of early lung specification and branching morphogenesis.
    Pediatric research, 2005
    Co-Authors: David Warburton, Denise Tefft, Stijn De Langhe, Mathieu Unbekandt, Kasper Wang, Vincent Fleury, Saverio Bellusci, Arnaud Mailleux, Pierre-marie Del Moral, Wei Shi
    Abstract:

    The "hard wiring" encoded within the genome that determines the emergence of the Laryngotracheal Groove and subsequently early lung branching morphogenesis is mediated by finely regulated, interactive growth factor signaling mechanisms that determine the automaticity of branching, interbranch length, stereotypy of branching, left-right asymmetry, and finally gas diffusion surface area. The extracellular matrix is an important regulator as well as a target for growth factor signaling in lung branching morphogenesis and alveolarization. Coordination not only of epithelial but also endothelial branching morphogenesis determines bronchial branching and the eventual alveolar-capillary interface. Improved prospects for lung protection, repair, regeneration, and engineering will depend on more detailed understanding of these processes. Herein, we concisely review the functionally integrated morphogenetic signaling network comprising the critical bone morphogenetic protein, fibroblast growth factor, Sonic hedgehog, transforming growth factor-beta, vascular endothelial growth factor, and Wnt signaling pathways that specify and drive early embryonic lung morphogenesis.

Kasper Wang - One of the best experts on this subject based on the ideXlab platform.

  • Molecular Mechanisms of Early Lung Specification and Branching Morphogenesis
    Pediatric Research, 2005
    Co-Authors: David Warburton, Denise Tefft, Stijn De Langhe, Pierre-marie Del Moral, Mathieu Unbekandt, Vincent Fleury, Saverio Bellusci, Arnaud Mailleux, Kasper Wang
    Abstract:

    The “hard wiring” encoded within the genome that determines the emergence of the Laryngotracheal Groove and subsequently early lung branching morphogenesis is mediated by finely regulated, interactive growth factor signaling mechanisms that determine the automaticity of branching, interbranch length, stereotypy of branching, left-right asymmetry, and finally gas diffusion surface area. The extracellular matrix is an important regulator as well as a target for growth factor signaling in lung branching morphogenesis and alveolarization. Coordination not only of epithelial but also endothelial branching morphogenesis determines bronchial branching and the eventual alveolar-capillary interface. Improved prospects for lung protection, repair, regeneration, and engineering will depend on more detailed understanding of these processes. Herein, we concisely review the functionally integrated morphogenetic signaling network comprising the critical bone morphogenetic protein, fibroblast growth factor, Sonic hedgehog, transforming growth factor-β, vascular endothelial growth factor, and Wnt signaling pathways that specify and drive early embryonic lung morphogenesis.

  • Molecular mechanisms of early lung specification and branching morphogenesis.
    Pediatric research, 2005
    Co-Authors: David Warburton, Denise Tefft, Stijn De Langhe, Mathieu Unbekandt, Kasper Wang, Vincent Fleury, Saverio Bellusci, Arnaud Mailleux, Pierre-marie Del Moral, Wei Shi
    Abstract:

    The "hard wiring" encoded within the genome that determines the emergence of the Laryngotracheal Groove and subsequently early lung branching morphogenesis is mediated by finely regulated, interactive growth factor signaling mechanisms that determine the automaticity of branching, interbranch length, stereotypy of branching, left-right asymmetry, and finally gas diffusion surface area. The extracellular matrix is an important regulator as well as a target for growth factor signaling in lung branching morphogenesis and alveolarization. Coordination not only of epithelial but also endothelial branching morphogenesis determines bronchial branching and the eventual alveolar-capillary interface. Improved prospects for lung protection, repair, regeneration, and engineering will depend on more detailed understanding of these processes. Herein, we concisely review the functionally integrated morphogenetic signaling network comprising the critical bone morphogenetic protein, fibroblast growth factor, Sonic hedgehog, transforming growth factor-beta, vascular endothelial growth factor, and Wnt signaling pathways that specify and drive early embryonic lung morphogenesis.

Nancy A. Mcnelly - One of the best experts on this subject based on the ideXlab platform.

  • Macrophage development: II. Early ontogeny of macrophage populations in brain, liver, and lungs of rat embryos as revealed by a lectin marker.
    The Anatomical record, 1992
    Co-Authors: Sergei P. Sorokin, Richard F. Hoyt, Dana G. Blunt, Nancy A. Mcnelly
    Abstract:

    Earliest origins of macrophage populations in the central nervous system, the liver, and the lungs were studied in rat embryos aged between 10.5-11 days and 14 days of gestation, based on light and electron microscopic identification of macrophages using peroxidase-coupled isolectin B4 of Griffonia simplicifolia (GSA I-B4), which recognizes alpha-D-galactose groups on the cell membrane. During embryonic life macrophages and their precursors are GSA I-B4-positive and generally bereft of peroxidase-positive granules. At 10.5 days the yolk sac and embryonic circulations have just become joined, the brain has five vesicles but nerve cells are little differentiated, the liver exists as a diverticulum of the gut with fingerlike extensions of hepatocytes, and the lungs as a Laryngotracheal Groove. Macrophages and/or their precursors occurred in small numbers in embryonic mesenchyme and blood vessels but showed no special affinity for either liver or lung rudiments. The developing brain was the first organ to be colonized, beginning on prenatal day 12. The liver followed between days 12 and 13 and was succeeded by the lungs, beginning between days 13 and 14. Dividing macrophages were present in these organs at the outset of colonization and throughout the duration of the embryo series, indicating that from the beginning, replication of resident cells contributes to growth of the local population. Granulocyte precursors were first apparent in the liver around day 13; they are also GSA-positive but are distinguished from macrophages by their content of peroxidase-positive granules. Organ cultures of 13-day liver and lungs, and 14-day brain tissue, indicate that whereas isolated liver fragments support the formation of both granulocytes and macrophages, only the latter develop in brain or lung cultures. A resident population of macrophages evidently is set up very early in these organs, well before white cells colonize the spleen, bone marrow, and other future blood forming regions. The events outlined are seen as stages in an embryo-wide process that leads to establishment of macrophage populations in various organs.

Wei Shi - One of the best experts on this subject based on the ideXlab platform.

  • Molecular mechanisms of early lung specification and branching morphogenesis.
    Pediatric research, 2005
    Co-Authors: David Warburton, Denise Tefft, Stijn De Langhe, Mathieu Unbekandt, Kasper Wang, Vincent Fleury, Saverio Bellusci, Arnaud Mailleux, Pierre-marie Del Moral, Wei Shi
    Abstract:

    The "hard wiring" encoded within the genome that determines the emergence of the Laryngotracheal Groove and subsequently early lung branching morphogenesis is mediated by finely regulated, interactive growth factor signaling mechanisms that determine the automaticity of branching, interbranch length, stereotypy of branching, left-right asymmetry, and finally gas diffusion surface area. The extracellular matrix is an important regulator as well as a target for growth factor signaling in lung branching morphogenesis and alveolarization. Coordination not only of epithelial but also endothelial branching morphogenesis determines bronchial branching and the eventual alveolar-capillary interface. Improved prospects for lung protection, repair, regeneration, and engineering will depend on more detailed understanding of these processes. Herein, we concisely review the functionally integrated morphogenetic signaling network comprising the critical bone morphogenetic protein, fibroblast growth factor, Sonic hedgehog, transforming growth factor-beta, vascular endothelial growth factor, and Wnt signaling pathways that specify and drive early embryonic lung morphogenesis.

Denise Tefft - One of the best experts on this subject based on the ideXlab platform.

  • Molecular Mechanisms of Early Lung Specification and Branching Morphogenesis
    Pediatric Research, 2005
    Co-Authors: David Warburton, Denise Tefft, Stijn De Langhe, Pierre-marie Del Moral, Mathieu Unbekandt, Vincent Fleury, Saverio Bellusci, Arnaud Mailleux, Kasper Wang
    Abstract:

    The “hard wiring” encoded within the genome that determines the emergence of the Laryngotracheal Groove and subsequently early lung branching morphogenesis is mediated by finely regulated, interactive growth factor signaling mechanisms that determine the automaticity of branching, interbranch length, stereotypy of branching, left-right asymmetry, and finally gas diffusion surface area. The extracellular matrix is an important regulator as well as a target for growth factor signaling in lung branching morphogenesis and alveolarization. Coordination not only of epithelial but also endothelial branching morphogenesis determines bronchial branching and the eventual alveolar-capillary interface. Improved prospects for lung protection, repair, regeneration, and engineering will depend on more detailed understanding of these processes. Herein, we concisely review the functionally integrated morphogenetic signaling network comprising the critical bone morphogenetic protein, fibroblast growth factor, Sonic hedgehog, transforming growth factor-β, vascular endothelial growth factor, and Wnt signaling pathways that specify and drive early embryonic lung morphogenesis.

  • Molecular mechanisms of early lung specification and branching morphogenesis.
    Pediatric research, 2005
    Co-Authors: David Warburton, Denise Tefft, Stijn De Langhe, Mathieu Unbekandt, Kasper Wang, Vincent Fleury, Saverio Bellusci, Arnaud Mailleux, Pierre-marie Del Moral, Wei Shi
    Abstract:

    The "hard wiring" encoded within the genome that determines the emergence of the Laryngotracheal Groove and subsequently early lung branching morphogenesis is mediated by finely regulated, interactive growth factor signaling mechanisms that determine the automaticity of branching, interbranch length, stereotypy of branching, left-right asymmetry, and finally gas diffusion surface area. The extracellular matrix is an important regulator as well as a target for growth factor signaling in lung branching morphogenesis and alveolarization. Coordination not only of epithelial but also endothelial branching morphogenesis determines bronchial branching and the eventual alveolar-capillary interface. Improved prospects for lung protection, repair, regeneration, and engineering will depend on more detailed understanding of these processes. Herein, we concisely review the functionally integrated morphogenetic signaling network comprising the critical bone morphogenetic protein, fibroblast growth factor, Sonic hedgehog, transforming growth factor-beta, vascular endothelial growth factor, and Wnt signaling pathways that specify and drive early embryonic lung morphogenesis.