Social interactions among epithelial cells during tracheal branching morphogenesis

Many organs are composed of tubular networks that arise by branching morphogenesis in which cells bud from an epithelium and organize into a tube. Fibroblast growth factors (FGFs) and other signalling molecules have been shown to guide branch budding and outgrowth, but it is not known how epithelial cells coordinate their movements and morphogenesis. Here we use genetic mosaic analysis in Drosophila melanogaster to show that there are two functionally distinct classes of cells in budding tracheal branches: cells at the tip that respond directly to Branchless FGF and lead branch outgrowth, and trailing cells that receive a secondary signal to follow the lead cells and form a tube. These roles are not pre-specified; rather, there is competition between cells such that those with the highest FGF receptor activity take the lead positions, whereas those with less FGF receptor activity assume subsidiary positions and form the branch stalk. Competition appears to involve Notch-mediated lateral inhibition that prevents extra cells from assuming the lead. There may also be cooperation between budding cells, because in a mosaic epithelium, cells that cannot respond to the chemoattractant, or respond only poorly, allow other cells in the epithelium to move ahead of them.

[1]  S. Hayashi,et al.  Interplay of Notch and FGF signaling restricts cell fate and MAPK activation in the Drosophila trachea. , 1999, Development.

[2]  Nobuyuki Itoh,et al.  Tube or not tube: remodeling epithelial tissues by branching morphogenesis. , 2003, Developmental cell.

[3]  B. Hogan,et al.  Bmp4 and Fgf10 play opposing roles during lung bud morphogenesis. , 2000, Development.

[4]  M. Krasnow,et al.  serpentine and vermiform Encode Matrix Proteins with Chitin Binding and Deacetylation Domains that Limit Tracheal Tube Length in Drosophila , 2006, Current Biology.

[5]  B. Shilo,et al.  breathless, a Drosophila FGF receptor homolog, is essential for migration of tracheal and specific midline glial cells. , 1992, Genes & development.

[6]  M. Affolter,et al.  Distinct roles for two receptor tyrosine kinases in epithelial branching morphogenesis in Drosophila. , 2005, Developmental cell.

[7]  N. Hacohen,et al.  sprouty Encodes a Novel Antagonist of FGF Signaling that Patterns Apical Branching of the Drosophila Airways , 1998, Cell.

[8]  F. Costantini,et al.  The role of GDNF/Ret signaling in ureteric bud cell fate and branching morphogenesis. , 2005, Developmental cell.

[9]  Matthew Freeman,et al.  Sprouty, an Intracellular Inhibitor of Ras Signaling , 1999, Cell.

[10]  N. Perrimon,et al.  Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. , 1993, Development.

[11]  B. Hogan,et al.  Organogenesis: Molecular Mechanisms Of Tubulogenesis , 2002, Nature Reviews Genetics.

[12]  B. Shilo,et al.  MAP kinase in situ activation atlas during Drosophila embryogenesis. , 1997, Development.

[13]  A. McMahon,et al.  GDNF induces branching and increased cell proliferation in the ureter of the mouse. , 1997, Developmental biology.

[14]  M. Affolter,et al.  In vivo imaging reveals different cellular functions for FGF and Dpp signaling in tracheal branching morphogenesis. , 2002, Developmental cell.

[15]  W. Cardoso,et al.  FGF-10 is a chemotactic factor for distal epithelial buds during lung development. , 1998, Developmental biology.

[16]  K. Golic Site-specific recombination between homologous chromosomes in Drosophila. , 1991, Science.

[17]  M. Krasnow,et al.  Genetic control of branching morphogenesis. , 1999, Science.

[18]  S. Hayashi,et al.  Control of tracheal tubulogenesis by Wingless signaling. , 2000, Development.

[19]  M. Metzstein,et al.  Branching morphogenesis of the Drosophila tracheal system. , 2003, Annual review of cell and developmental biology.

[20]  K. Alitalo,et al.  VEGF guides angiogenic sprouting utilizing endothelial tip cell filopodia , 2003, The Journal of cell biology.

[21]  Eric Johnson,et al.  Oxygen Regulation of Airway Branching in Drosophila Is Mediated by Branchless FGF , 1999, Cell.

[22]  M. Krasnow,et al.  branchless Encodes a Drosophila FGF Homolog That Controls Tracheal Cell Migration and the Pattern of Branching , 1996, Cell.

[23]  C. Klämbt,et al.  The Drosophila gene pointed encodes two ETS-like proteins which are involved in the development of the midline glial cells. , 1993, Development.

[24]  F. Imam,et al.  stumps, a Drosophila gene required for fibroblast growth factor (FGF)-directed migrations of tracheal and mesodermal cells. , 1999, Genetics.

[25]  M. Affolter,et al.  The Drosophila protein Dof is specifically required for FGF signaling. , 1998, Molecular cell.

[26]  M. Llimargas Wingless and its signalling pathway have common and separable functions during tracheal development. , 2000, Development.

[27]  N. Hacohen,et al.  Development of the Drosophila tracheal system occurs by a series of morphologically distinct but genetically coupled branching events. , 1996, Development.

[28]  M. Llimargas,et al.  The Notch pathway helps to pattern the tips of the Drosophila tracheal branches by selecting cell fates. , 1999, Development.