Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans.

In mammals, Bone Morphogenetic Protein (BMP) pathway signaling is important for the growth and homeostasis of extracellular matrix, including basement membrane remodeling, scarring, and bone growth. A conserved BMP member in Caenorhabditis elegans, DBL-1, regulates body length in a dose-sensitive ma...

Full description

Bibliographic Details
Main Authors: Robbie D Schultz, Emily E Bennett, E Ann Ellis, Tina L Gumienny
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4094471?pdf=render
id doaj-416b4957938248e189c192ff6a5c15b0
record_format Article
spelling doaj-416b4957938248e189c192ff6a5c15b02020-11-25T02:32:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0197e10192910.1371/journal.pone.0101929Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans.Robbie D SchultzEmily E BennettE Ann EllisTina L GumiennyIn mammals, Bone Morphogenetic Protein (BMP) pathway signaling is important for the growth and homeostasis of extracellular matrix, including basement membrane remodeling, scarring, and bone growth. A conserved BMP member in Caenorhabditis elegans, DBL-1, regulates body length in a dose-sensitive manner. Loss of DBL-1 pathway signaling also results in increased anesthetic sensitivity. However, the physiological basis of these pleiotropic phenotypes is largely unknown. We created a DBL-1 over-expressing strain and show that sensitivity to anesthetics is inversely related to the dose of DBL-1. Using pharmacological, genetic analyses, and a novel dye permeability assay for live, microwave-treated animals, we confirm that DBL-1 is required for the barrier function of the cuticle, a specialized extracellular matrix. We show that DBL-1 signaling is required to prevent animals from forming tail-entangled aggregates in liquid. Stripping lipids off the surface of wild-type animals recapitulates this phenotype. Finally, we find that DBL-1 signaling affects ultrastructure of the nematode cuticle in a dose-dependent manner, as surface lipid content and cuticular organization are disrupted in animals with genetically altered DBL-1 levels. We propose that the lipid layer coating the nematode cuticle normally prevents tail entanglement, and that reduction of this layer by loss of DBL-1 signaling promotes aggregation. This work provides a physiological mechanism that unites the DBL-1 signaling pathway roles of not only body size regulation and drug responsiveness, but also the novel Hoechst 33342 staining and aggregation phenotypes, through barrier function, content, and organization of the cuticle.http://europepmc.org/articles/PMC4094471?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Robbie D Schultz
Emily E Bennett
E Ann Ellis
Tina L Gumienny
spellingShingle Robbie D Schultz
Emily E Bennett
E Ann Ellis
Tina L Gumienny
Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans.
PLoS ONE
author_facet Robbie D Schultz
Emily E Bennett
E Ann Ellis
Tina L Gumienny
author_sort Robbie D Schultz
title Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans.
title_short Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans.
title_full Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans.
title_fullStr Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans.
title_full_unstemmed Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans.
title_sort regulation of extracellular matrix organization by bmp signaling in caenorhabditis elegans.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description In mammals, Bone Morphogenetic Protein (BMP) pathway signaling is important for the growth and homeostasis of extracellular matrix, including basement membrane remodeling, scarring, and bone growth. A conserved BMP member in Caenorhabditis elegans, DBL-1, regulates body length in a dose-sensitive manner. Loss of DBL-1 pathway signaling also results in increased anesthetic sensitivity. However, the physiological basis of these pleiotropic phenotypes is largely unknown. We created a DBL-1 over-expressing strain and show that sensitivity to anesthetics is inversely related to the dose of DBL-1. Using pharmacological, genetic analyses, and a novel dye permeability assay for live, microwave-treated animals, we confirm that DBL-1 is required for the barrier function of the cuticle, a specialized extracellular matrix. We show that DBL-1 signaling is required to prevent animals from forming tail-entangled aggregates in liquid. Stripping lipids off the surface of wild-type animals recapitulates this phenotype. Finally, we find that DBL-1 signaling affects ultrastructure of the nematode cuticle in a dose-dependent manner, as surface lipid content and cuticular organization are disrupted in animals with genetically altered DBL-1 levels. We propose that the lipid layer coating the nematode cuticle normally prevents tail entanglement, and that reduction of this layer by loss of DBL-1 signaling promotes aggregation. This work provides a physiological mechanism that unites the DBL-1 signaling pathway roles of not only body size regulation and drug responsiveness, but also the novel Hoechst 33342 staining and aggregation phenotypes, through barrier function, content, and organization of the cuticle.
url http://europepmc.org/articles/PMC4094471?pdf=render
work_keys_str_mv AT robbiedschultz regulationofextracellularmatrixorganizationbybmpsignalingincaenorhabditiselegans
AT emilyebennett regulationofextracellularmatrixorganizationbybmpsignalingincaenorhabditiselegans
AT eannellis regulationofextracellularmatrixorganizationbybmpsignalingincaenorhabditiselegans
AT tinalgumienny regulationofextracellularmatrixorganizationbybmpsignalingincaenorhabditiselegans
_version_ 1724819481637683200