Literature DB >> 22083894

Drosophila as a model for epithelial tube formation.

Rika Maruyama1, Deborah J Andrew.   

Abstract

Epithelial tubular organs are essential for life in higher organisms and include the pancreas and other secretory organs that function as biological factories for the synthesis and delivery of secreted enzymes, hormones, and nutrients essential for tissue homeostasis and viability. The lungs, which are necessary for gas exchange, vocalization, and maintaining blood pH, are organized as highly branched tubular epithelia. Tubular organs include arteries, veins, and lymphatics, high-speed passageways for delivery and uptake of nutrients, liquids, gases, and immune cells. The kidneys and components of the reproductive system are also epithelial tubes. Both the heart and central nervous system of many vertebrates begin as epithelial tubes. Thus, it is not surprising that defects in tube formation and maintenance underlie many human diseases. Accordingly, a thorough understanding how tubes form and are maintained is essential to developing better diagnostics and therapeutics. Among the best-characterized tubular organs are the Drosophila salivary gland and trachea, organs whose relative simplicity have allowed for in depth analysis of gene function, yielding key mechanistic insight into tube initiation, remodeling and maintenance. Here, we review our current understanding of salivary gland and trachea formation - highlighting recent discoveries into how these organs attain their final form and function.
Copyright © 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 22083894      PMCID: PMC3922621          DOI: 10.1002/dvdy.22775

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  177 in total

1.  The role of the tracheae and musculature during pathfinding of Drosophila embryonic sensory axons.

Authors:  A Younossi-Hartenstein; V Hartenstein
Journal:  Dev Biol       Date:  1993-08       Impact factor: 3.582

2.  The Drosophila FGF-R homolog is expressed in the embryonic tracheal system and appears to be required for directed tracheal cell extension.

Authors:  L Glazer; B Z Shilo
Journal:  Genes Dev       Date:  1991-04       Impact factor: 11.361

3.  Cell fate specification in the Drosophila salivary gland: the integration of homeotic gene function with the DPP signaling cascade.

Authors:  K D Henderson; D D Isaac; D J Andrew
Journal:  Dev Biol       Date:  1999-01-01       Impact factor: 3.582

4.  CRUMBS is involved in the control of apical protein targeting during Drosophila epithelial development.

Authors:  A Wodarz; F Grawe; E Knust
Journal:  Mech Dev       Date:  1993-12       Impact factor: 1.882

5.  breathless, a Drosophila FGF receptor homolog, is essential for migration of tracheal and specific midline glial cells.

Authors:  C Klämbt; L Glazer; B Z Shilo
Journal:  Genes Dev       Date:  1992-09       Impact factor: 11.361

6.  Elucidation of the role of breathless, a Drosophila FGF receptor homolog, in tracheal cell migration.

Authors:  M Reichman-Fried; B Dickson; E Hafen; B Z Shilo
Journal:  Genes Dev       Date:  1994-02-15       Impact factor: 11.361

7.  Organogenesis in Drosophila melanogaster: embryonic salivary gland determination is controlled by homeotic and dorsoventral patterning genes.

Authors:  S Panzer; D Weigel; S K Beckendorf
Journal:  Development       Date:  1992-01       Impact factor: 6.868

8.  Targeted gene expression as a means of altering cell fates and generating dominant phenotypes.

Authors:  A H Brand; N Perrimon
Journal:  Development       Date:  1993-06       Impact factor: 6.868

9.  Setting limits on homeotic gene function: restraint of Sex combs reduced activity by teashirt and other homeotic genes.

Authors:  D J Andrew; M A Horner; M G Petitt; S M Smolik; M P Scott
Journal:  EMBO J       Date:  1994-03-01       Impact factor: 11.598

10.  The transcription factors KNIRPS and KNIRPS RELATED control cell migration and branch morphogenesis during Drosophila tracheal development.

Authors:  C K Chen; R P Kühnlein; K G Eulenberg; S Vincent; M Affolter; R Schuh
Journal:  Development       Date:  1998-12       Impact factor: 6.868

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  32 in total

1.  Extracellular Mipp1 Activity Confers Migratory Advantage to Epithelial Cells during Collective Migration.

Authors:  Yim Ling Cheng; Deborah J Andrew
Journal:  Cell Rep       Date:  2015-11-25       Impact factor: 9.423

Review 2.  Tubulogenesis.

Authors:  M Luisa Iruela-Arispe; Greg J Beitel
Journal:  Development       Date:  2013-07       Impact factor: 6.868

Review 3.  A holey pursuit: lumen formation in the developing kidney.

Authors:  Denise K Marciano
Journal:  Pediatr Nephrol       Date:  2016-02-22       Impact factor: 3.714

Review 4.  Key roles of Arf small G proteins and biosynthetic trafficking for animal development.

Authors:  Francisco F Rodrigues; Tony J C Harris
Journal:  Small GTPases       Date:  2017-04-17

5.  Tubular Excretory Canal Structure Depends on Intermediate Filaments EXC-2 and IFA-4 in Caenorhabditis elegans.

Authors:  Hikmat Al-Hashimi; David H Hall; Brian D Ackley; Erik A Lundquist; Matthew Buechner
Journal:  Genetics       Date:  2018-06-26       Impact factor: 4.562

Review 6.  Branching morphogenesis: from cells to organs and back.

Authors:  Amanda Ochoa-Espinosa; Markus Affolter
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-10-01       Impact factor: 10.005

Review 7.  Evolutionary origins of the blood vascular system and endothelium.

Authors:  R Monahan-Earley; A M Dvorak; W C Aird
Journal:  J Thromb Haemost       Date:  2013-06       Impact factor: 5.824

Review 8.  Aging and the clock: Perspective from flies to humans.

Authors:  Aliza K De Nobrega; Lisa C Lyons
Journal:  Eur J Neurosci       Date:  2018-10-30       Impact factor: 3.386

Review 9.  The Caenorhabditis elegans Excretory System: A Model for Tubulogenesis, Cell Fate Specification, and Plasticity.

Authors:  Meera V Sundaram; Matthew Buechner
Journal:  Genetics       Date:  2016-05       Impact factor: 4.562

10.  The secreted AdamTS-A metalloprotease is required for collective cell migration.

Authors:  Afshan Ismat; Alan M Cheshire; Deborah J Andrew
Journal:  Development       Date:  2013-03-27       Impact factor: 6.868

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