Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish

The sense of smell in vertebrates is detected by specialized sensory neurons derived from the peripheral nervous system. Classically, it has been presumed that the olfactory placode forms all olfactory sensory neurons. In contrast, we show that the cranial neural crest is the primary source of micro...

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Main Authors: Ankur Saxena, Brian N Peng, Marianne E Bronner
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2013-03-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/00336
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spelling doaj-c77a03a135f94fb58d7006ffa3f3451a2021-05-04T21:29:33ZengeLife Sciences Publications LtdeLife2050-084X2013-03-01210.7554/eLife.00336Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafishAnkur Saxena0Brian N Peng1Marianne E Bronner2Division of Biology, California Institute of Technology, Pasadena, United StatesDivision of Biology, California Institute of Technology, Pasadena, United StatesDivision of Biology, California Institute of Technology, Pasadena, United StatesThe sense of smell in vertebrates is detected by specialized sensory neurons derived from the peripheral nervous system. Classically, it has been presumed that the olfactory placode forms all olfactory sensory neurons. In contrast, we show that the cranial neural crest is the primary source of microvillous sensory neurons within the olfactory epithelium of zebrafish embryos. Using photoconversion-based fate mapping and live cell tracking coupled with laser ablation, we followed neural crest precursors as they migrated from the neural tube to the nasal cavity. A subset that coexpressed Sox10 protein and a neurogenin1 reporter ingressed into the olfactory epithelium and differentiated into microvillous sensory neurons. Timed loss-of-function analysis revealed a critical role for Sox10 in microvillous neurogenesis. Taken together, these findings directly demonstrate a heretofore unknown contribution of the cranial neural crest to olfactory sensory neurons in zebrafish and provide important insights into the assembly of the nascent olfactory system.https://elifesciences.org/articles/00336neural crest migrationolfactory developmentmicrovillous sensory neuronneurogenesis
collection DOAJ
language English
format Article
sources DOAJ
author Ankur Saxena
Brian N Peng
Marianne E Bronner
spellingShingle Ankur Saxena
Brian N Peng
Marianne E Bronner
Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish
eLife
neural crest migration
olfactory development
microvillous sensory neuron
neurogenesis
author_facet Ankur Saxena
Brian N Peng
Marianne E Bronner
author_sort Ankur Saxena
title Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish
title_short Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish
title_full Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish
title_fullStr Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish
title_full_unstemmed Sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish
title_sort sox10-dependent neural crest origin of olfactory microvillous neurons in zebrafish
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2013-03-01
description The sense of smell in vertebrates is detected by specialized sensory neurons derived from the peripheral nervous system. Classically, it has been presumed that the olfactory placode forms all olfactory sensory neurons. In contrast, we show that the cranial neural crest is the primary source of microvillous sensory neurons within the olfactory epithelium of zebrafish embryos. Using photoconversion-based fate mapping and live cell tracking coupled with laser ablation, we followed neural crest precursors as they migrated from the neural tube to the nasal cavity. A subset that coexpressed Sox10 protein and a neurogenin1 reporter ingressed into the olfactory epithelium and differentiated into microvillous sensory neurons. Timed loss-of-function analysis revealed a critical role for Sox10 in microvillous neurogenesis. Taken together, these findings directly demonstrate a heretofore unknown contribution of the cranial neural crest to olfactory sensory neurons in zebrafish and provide important insights into the assembly of the nascent olfactory system.
topic neural crest migration
olfactory development
microvillous sensory neuron
neurogenesis
url https://elifesciences.org/articles/00336
work_keys_str_mv AT ankursaxena sox10dependentneuralcrestoriginofolfactorymicrovillousneuronsinzebrafish
AT briannpeng sox10dependentneuralcrestoriginofolfactorymicrovillousneuronsinzebrafish
AT marianneebronner sox10dependentneuralcrestoriginofolfactorymicrovillousneuronsinzebrafish
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