Cargando…

The cell adhesion molecule Fasciclin2 regulates brush border length and organization in Drosophila renal tubules

Multicellular organisms rely on cell adhesion molecules to coordinate cell–cell interactions, and to provide navigational cues during tissue formation. In Drosophila, Fasciclin 2 (Fas2) has been intensively studied due to its role in nervous system development and maintenance; yet, Fas2 is most abun...

Descripción completa

Detalles Bibliográficos
Autores principales: Halberg, Kenneth A., Rainey, Stephanie M., Veland, Iben R., Neuert, Helen, Dornan, Anthony J., Klämbt, Christian, Davies, Shireen-Anne, Dow, Julian A. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833865/
https://www.ncbi.nlm.nih.gov/pubmed/27072072
http://dx.doi.org/10.1038/ncomms11266
_version_ 1782427397594808320
author Halberg, Kenneth A.
Rainey, Stephanie M.
Veland, Iben R.
Neuert, Helen
Dornan, Anthony J.
Klämbt, Christian
Davies, Shireen-Anne
Dow, Julian A. T.
author_facet Halberg, Kenneth A.
Rainey, Stephanie M.
Veland, Iben R.
Neuert, Helen
Dornan, Anthony J.
Klämbt, Christian
Davies, Shireen-Anne
Dow, Julian A. T.
author_sort Halberg, Kenneth A.
collection PubMed
description Multicellular organisms rely on cell adhesion molecules to coordinate cell–cell interactions, and to provide navigational cues during tissue formation. In Drosophila, Fasciclin 2 (Fas2) has been intensively studied due to its role in nervous system development and maintenance; yet, Fas2 is most abundantly expressed in the adult renal (Malpighian) tubule rather than in neuronal tissues. The role Fas2 serves in this epithelium is unknown. Here we show that Fas2 is essential to brush border maintenance in renal tubules of Drosophila. Fas2 is dynamically expressed during tubule morphogenesis, localizing to the brush border whenever the tissue is transport competent. Genetic manipulations of Fas2 expression levels impact on both microvilli length and organization, which in turn dramatically affect stimulated rates of fluid secretion by the tissue. Consequently, we demonstrate a radically different role for this well-known cell adhesion molecule, and propose that Fas2-mediated intermicrovillar homophilic adhesion complexes help stabilize the brush border.
format Online
Article
Text
id pubmed-4833865
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-48338652016-05-02 The cell adhesion molecule Fasciclin2 regulates brush border length and organization in Drosophila renal tubules Halberg, Kenneth A. Rainey, Stephanie M. Veland, Iben R. Neuert, Helen Dornan, Anthony J. Klämbt, Christian Davies, Shireen-Anne Dow, Julian A. T. Nat Commun Article Multicellular organisms rely on cell adhesion molecules to coordinate cell–cell interactions, and to provide navigational cues during tissue formation. In Drosophila, Fasciclin 2 (Fas2) has been intensively studied due to its role in nervous system development and maintenance; yet, Fas2 is most abundantly expressed in the adult renal (Malpighian) tubule rather than in neuronal tissues. The role Fas2 serves in this epithelium is unknown. Here we show that Fas2 is essential to brush border maintenance in renal tubules of Drosophila. Fas2 is dynamically expressed during tubule morphogenesis, localizing to the brush border whenever the tissue is transport competent. Genetic manipulations of Fas2 expression levels impact on both microvilli length and organization, which in turn dramatically affect stimulated rates of fluid secretion by the tissue. Consequently, we demonstrate a radically different role for this well-known cell adhesion molecule, and propose that Fas2-mediated intermicrovillar homophilic adhesion complexes help stabilize the brush border. Nature Publishing Group 2016-04-13 /pmc/articles/PMC4833865/ /pubmed/27072072 http://dx.doi.org/10.1038/ncomms11266 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Halberg, Kenneth A.
Rainey, Stephanie M.
Veland, Iben R.
Neuert, Helen
Dornan, Anthony J.
Klämbt, Christian
Davies, Shireen-Anne
Dow, Julian A. T.
The cell adhesion molecule Fasciclin2 regulates brush border length and organization in Drosophila renal tubules
title The cell adhesion molecule Fasciclin2 regulates brush border length and organization in Drosophila renal tubules
title_full The cell adhesion molecule Fasciclin2 regulates brush border length and organization in Drosophila renal tubules
title_fullStr The cell adhesion molecule Fasciclin2 regulates brush border length and organization in Drosophila renal tubules
title_full_unstemmed The cell adhesion molecule Fasciclin2 regulates brush border length and organization in Drosophila renal tubules
title_short The cell adhesion molecule Fasciclin2 regulates brush border length and organization in Drosophila renal tubules
title_sort cell adhesion molecule fasciclin2 regulates brush border length and organization in drosophila renal tubules
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833865/
https://www.ncbi.nlm.nih.gov/pubmed/27072072
http://dx.doi.org/10.1038/ncomms11266
work_keys_str_mv AT halbergkennetha thecelladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT raineystephaniem thecelladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT velandibenr thecelladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT neuerthelen thecelladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT dornananthonyj thecelladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT klambtchristian thecelladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT daviesshireenanne thecelladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT dowjulianat thecelladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT halbergkennetha celladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT raineystephaniem celladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT velandibenr celladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT neuerthelen celladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT dornananthonyj celladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT klambtchristian celladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT daviesshireenanne celladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules
AT dowjulianat celladhesionmoleculefasciclin2regulatesbrushborderlengthandorganizationindrosophilarenaltubules