Literature DB >> 27274435

Drosophila Imaginal Discs as a Model of Epithelial Wound Repair and Regeneration.

Rachel Smith-Bolton1.   

Abstract

Significance: The Drosophila larval imaginal discs, which form the adult fly during metamorphosis, are an established model system for the study of epithelial tissue damage. The disc proper is a simple columnar epithelium, but it contains complex patterning and cell-fate specification, and is genetically tractable. These features enable unbiased genetic screens to identify genes involved in all aspects of the wound response, from sensing damage to wound closure, initiation of regeneration, and re-establishment of proper cell fates. Identification of the genes that facilitate epithelial wound closure and regeneration will enable development of more sophisticated wound treatments for clinical use. Recent Advances: Imaginal disc epithelia can be damaged in many different ways, including fragmentation, induction of cell death, and irradiation. Recent work has demonstrated that the tissue's response to damage varies depending on how the wound was induced. Here, we summarize the different responses activated in these epithelial tissues after the different types of damage. Critical Issues: These studies highlight that not all wounds elicit the same response from the surrounding tissue. A complete understanding of the various wound-healing mechanisms in Drosophila will be a first step in understanding how to manage damaged human tissues and optimize healing in different clinical contexts. Future Directions: Further work is necessary to understand the similarities and differences among an epithelial tissue's responses to different insults. Ongoing studies will identify the genes and pathways employed by injured imaginal discs. Thus, work in this genetically tractable system complements work in more conventional wound-healing models.

Entities:  

Year:  2016        PMID: 27274435      PMCID: PMC4876537          DOI: 10.1089/wound.2014.0547

Source DB:  PubMed          Journal:  Adv Wound Care (New Rochelle)        ISSN: 2162-1918            Impact factor:   4.730


  65 in total

1.  Maintenance of imaginal disc plasticity and regenerative potential in Drosophila by p53.

Authors:  Brent S Wells; Laura A Johnston
Journal:  Dev Biol       Date:  2011-10-19       Impact factor: 3.582

2.  Role of Jun N-terminal Kinase (JNK) signaling in the wound healing and regeneration of a Drosophila melanogaster wing imaginal disc.

Authors:  Jaakko Mattila; Leonid Omelyanchuk; Satu Kyttälä; Heikki Turunen; Seppo Nokkala
Journal:  Int J Dev Biol       Date:  2005       Impact factor: 2.203

3.  Regeneration and duplication following operations in situ on the imaginal discs of Drosophila melanogaster.

Authors:  P J Bryant
Journal:  Dev Biol       Date:  1971-12       Impact factor: 3.582

4.  DRONC coordinates cell death and compensatory proliferation.

Authors:  Shu Kondo; Nanami Senoo-Matsuda; Yasushi Hiromi; Masayuki Miura
Journal:  Mol Cell Biol       Date:  2006-10       Impact factor: 4.272

5.  Secreted peptide Dilp8 coordinates Drosophila tissue growth with developmental timing.

Authors:  Julien Colombani; Ditte S Andersen; Pierre Léopold
Journal:  Science       Date:  2012-05-04       Impact factor: 47.728

6.  Compensatory proliferation in Drosophila imaginal discs requires Dronc-dependent p53 activity.

Authors:  Brent S Wells; Eri Yoshida; Laura A Johnston
Journal:  Curr Biol       Date:  2006-08-22       Impact factor: 10.834

7.  Gene expression following induction of regeneration in Drosophila wing imaginal discs. Expression profile of regenerating wing discs.

Authors:  Enrique Blanco; Marina Ruiz-Romero; Sergi Beltran; Manel Bosch; Adrià Punset; Florenci Serras; Montserrat Corominas
Journal:  BMC Dev Biol       Date:  2010-09-02       Impact factor: 1.978

8.  Three genes control the timing, the site and the size of blastema formation in Drosophila.

Authors:  Kimberly D McClure; Anne Sustar; Gerold Schubiger
Journal:  Dev Biol       Date:  2008-04-15       Impact factor: 3.582

9.  Sustained production of ROS triggers compensatory proliferation and is required for regeneration to proceed.

Authors:  Carole Gauron; Christine Rampon; Mohamed Bouzaffour; Eliane Ipendey; Jérémie Teillon; Michel Volovitch; Sophie Vriz
Journal:  Sci Rep       Date:  2013       Impact factor: 4.379

10.  Transgressions of compartment boundaries and cell reprogramming during regeneration in Drosophila.

Authors:  Salvador C Herrera; Ginés Morata
Journal:  Elife       Date:  2014-04-22       Impact factor: 8.140

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  5 in total

Review 1.  An unexpected friend - ROS in apoptosis-induced compensatory proliferation: Implications for regeneration and cancer.

Authors:  Neha Diwanji; Andreas Bergmann
Journal:  Semin Cell Dev Biol       Date:  2017-07-05       Impact factor: 7.727

2.  Chemical Amputation and Regeneration of the Pharynx in the Planarian Schmidtea mediterranea.

Authors:  Divya A Shiroor; Tisha E Bohr; Carolyn E Adler
Journal:  J Vis Exp       Date:  2018-03-26       Impact factor: 1.355

Review 3.  Killers creating new life: caspases drive apoptosis-induced proliferation in tissue repair and disease.

Authors:  Caitlin E Fogarty; Andreas Bergmann
Journal:  Cell Death Differ       Date:  2017-03-31       Impact factor: 15.828

4.  The many fates of tissue regeneration.

Authors:  Christopher Abdullah; Robert J Duronio
Journal:  PLoS Genet       Date:  2018-11-21       Impact factor: 5.917

5.  Bioinformatics analysis of fibroblasts exposed to TGF‑β at the early proliferation phase of wound repair.

Authors:  Bobin Mi; Guohui Liu; Wu Zhou; Huijuan Lv; Kun Zha; Yi Liu; Qipeng Wu; Jing Liu
Journal:  Mol Med Rep       Date:  2017-09-26       Impact factor: 2.952

  5 in total

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