A small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.

Adult vertebrates have retained the ability to regenerate peripheral nerves after injury, although regeneration is frequently incomplete, often leading to functional impairments. Small molecule screens using whole organisms have high potential to identify biologically relevant targets, yet currently...

Full description

Bibliographic Details
Main Authors: Juliane Bremer, Julianne Skinner, Michael Granato
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5456414?pdf=render
id doaj-b31b3cf59cd74179a34d701017427ded
record_format Article
spelling doaj-b31b3cf59cd74179a34d701017427ded2020-11-24T22:03:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01126e017885410.1371/journal.pone.0178854A small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.Juliane BremerJulianne SkinnerMichael GranatoAdult vertebrates have retained the ability to regenerate peripheral nerves after injury, although regeneration is frequently incomplete, often leading to functional impairments. Small molecule screens using whole organisms have high potential to identify biologically relevant targets, yet currently available assays for in vivo peripheral nerve regeneration are either very laborious and/or require complex technology. Here we take advantage of the optical transparency of larval zebrafish to develop a simple and fast pectoral fin removal assay that measures peripheral nerve regeneration in vivo. Twenty-four hours after fin amputation we observe robust and stereotyped nerve regrowth at the fin base. Similar to laser mediated nerve transection, nerve regrowth after fin amputation requires Schwann cells and FGF signaling, confirming that the fin amputation assay identifies pathways relevant for peripheral nerve regeneration. From a library of small molecules with known targets, we identified 21 compounds that impair peripheral nerve regeneration. Several of these compounds target known regulators of nerve regeneration, further validating the fin removal assay. Twelve of the identified compounds affect targets not previously known to control peripheral nerve regeneration. Using a laser-mediated nerve transection assay we tested ten of those compounds and confirmed six of these compounds to impair peripheral nerve regeneration: an EGFR inhibitor, a glucocorticoid, prostaglandin D2, a retinoic acid agonist, an inhibitor of calcium channels and a topoisomerase I inhibitor. Thus, we established a technically simple assay to rapidly identify valuable entry points into pathways critical for vertebrate peripheral nerve regeneration.http://europepmc.org/articles/PMC5456414?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Juliane Bremer
Julianne Skinner
Michael Granato
spellingShingle Juliane Bremer
Julianne Skinner
Michael Granato
A small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.
PLoS ONE
author_facet Juliane Bremer
Julianne Skinner
Michael Granato
author_sort Juliane Bremer
title A small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.
title_short A small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.
title_full A small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.
title_fullStr A small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.
title_full_unstemmed A small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.
title_sort small molecule screen identifies in vivo modulators of peripheral nerve regeneration in zebrafish.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Adult vertebrates have retained the ability to regenerate peripheral nerves after injury, although regeneration is frequently incomplete, often leading to functional impairments. Small molecule screens using whole organisms have high potential to identify biologically relevant targets, yet currently available assays for in vivo peripheral nerve regeneration are either very laborious and/or require complex technology. Here we take advantage of the optical transparency of larval zebrafish to develop a simple and fast pectoral fin removal assay that measures peripheral nerve regeneration in vivo. Twenty-four hours after fin amputation we observe robust and stereotyped nerve regrowth at the fin base. Similar to laser mediated nerve transection, nerve regrowth after fin amputation requires Schwann cells and FGF signaling, confirming that the fin amputation assay identifies pathways relevant for peripheral nerve regeneration. From a library of small molecules with known targets, we identified 21 compounds that impair peripheral nerve regeneration. Several of these compounds target known regulators of nerve regeneration, further validating the fin removal assay. Twelve of the identified compounds affect targets not previously known to control peripheral nerve regeneration. Using a laser-mediated nerve transection assay we tested ten of those compounds and confirmed six of these compounds to impair peripheral nerve regeneration: an EGFR inhibitor, a glucocorticoid, prostaglandin D2, a retinoic acid agonist, an inhibitor of calcium channels and a topoisomerase I inhibitor. Thus, we established a technically simple assay to rapidly identify valuable entry points into pathways critical for vertebrate peripheral nerve regeneration.
url http://europepmc.org/articles/PMC5456414?pdf=render
work_keys_str_mv AT julianebremer asmallmoleculescreenidentifiesinvivomodulatorsofperipheralnerveregenerationinzebrafish
AT julianneskinner asmallmoleculescreenidentifiesinvivomodulatorsofperipheralnerveregenerationinzebrafish
AT michaelgranato asmallmoleculescreenidentifiesinvivomodulatorsofperipheralnerveregenerationinzebrafish
AT julianebremer smallmoleculescreenidentifiesinvivomodulatorsofperipheralnerveregenerationinzebrafish
AT julianneskinner smallmoleculescreenidentifiesinvivomodulatorsofperipheralnerveregenerationinzebrafish
AT michaelgranato smallmoleculescreenidentifiesinvivomodulatorsofperipheralnerveregenerationinzebrafish
_version_ 1725831268710481920