Cargando…

Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents

Puberty is a critical period in mesocorticolimbic dopamine (DA) system development, particularly for the medial prefrontal cortex (mPFC) projection which achieves maturity in early adulthood. The guidance cue netrin-1 organizes neuronal networks by attracting or repelling cellular processes through...

Descripción completa

Detalles Bibliográficos
Autores principales: Manitt, Colleen, Labelle-Dumais, Cassandre, Eng, Conrad, Grant, Alanna, Mimee, Andrea, Stroh, Thomas, Flores, Cecilia
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900213/
https://www.ncbi.nlm.nih.gov/pubmed/20628609
http://dx.doi.org/10.1371/journal.pone.0011463
_version_ 1782183602878939136
author Manitt, Colleen
Labelle-Dumais, Cassandre
Eng, Conrad
Grant, Alanna
Mimee, Andrea
Stroh, Thomas
Flores, Cecilia
author_facet Manitt, Colleen
Labelle-Dumais, Cassandre
Eng, Conrad
Grant, Alanna
Mimee, Andrea
Stroh, Thomas
Flores, Cecilia
author_sort Manitt, Colleen
collection PubMed
description Puberty is a critical period in mesocorticolimbic dopamine (DA) system development, particularly for the medial prefrontal cortex (mPFC) projection which achieves maturity in early adulthood. The guidance cue netrin-1 organizes neuronal networks by attracting or repelling cellular processes through DCC (deleted in colorectal cancer) and UNC-5 homologue (UNC5H) receptors, respectively. We have shown that variations in netrin-1 receptor levels lead to selective reorganization of mPFC DA circuitry, and changes in DA-related behaviors, in transgenic mice and in rats. Significantly, these effects are only observed after puberty, suggesting that netrin-1 mediated effects on DA systems vary across development. Here we report on the normal expression of DCC and UNC5H in the ventral tegmental area (VTA) by DA neurons from embryonic life to adulthood, in both mice and rats. We show a dramatic and enduring pubertal change in the ratio of DCC:UNC5H receptors, reflecting a shift toward predominant UNC5H function. This shift in DCC:UNC5H ratio coincides with the pubertal emergence of UNC5H expression by VTA DA neurons. Although the distribution of DCC and UNC5H by VTA DA neurons changes during puberty, the pattern of netrin-1 immunoreactivity in these cells does not. Together, our findings suggest that DCC:UNC5H ratios in DA neurons at critical periods may have important consequences for the organization and function of mesocorticolimbic DA systems.
format Text
id pubmed-2900213
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-29002132010-07-13 Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents Manitt, Colleen Labelle-Dumais, Cassandre Eng, Conrad Grant, Alanna Mimee, Andrea Stroh, Thomas Flores, Cecilia PLoS One Research Article Puberty is a critical period in mesocorticolimbic dopamine (DA) system development, particularly for the medial prefrontal cortex (mPFC) projection which achieves maturity in early adulthood. The guidance cue netrin-1 organizes neuronal networks by attracting or repelling cellular processes through DCC (deleted in colorectal cancer) and UNC-5 homologue (UNC5H) receptors, respectively. We have shown that variations in netrin-1 receptor levels lead to selective reorganization of mPFC DA circuitry, and changes in DA-related behaviors, in transgenic mice and in rats. Significantly, these effects are only observed after puberty, suggesting that netrin-1 mediated effects on DA systems vary across development. Here we report on the normal expression of DCC and UNC5H in the ventral tegmental area (VTA) by DA neurons from embryonic life to adulthood, in both mice and rats. We show a dramatic and enduring pubertal change in the ratio of DCC:UNC5H receptors, reflecting a shift toward predominant UNC5H function. This shift in DCC:UNC5H ratio coincides with the pubertal emergence of UNC5H expression by VTA DA neurons. Although the distribution of DCC and UNC5H by VTA DA neurons changes during puberty, the pattern of netrin-1 immunoreactivity in these cells does not. Together, our findings suggest that DCC:UNC5H ratios in DA neurons at critical periods may have important consequences for the organization and function of mesocorticolimbic DA systems. Public Library of Science 2010-07-08 /pmc/articles/PMC2900213/ /pubmed/20628609 http://dx.doi.org/10.1371/journal.pone.0011463 Text en Manitt et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Manitt, Colleen
Labelle-Dumais, Cassandre
Eng, Conrad
Grant, Alanna
Mimee, Andrea
Stroh, Thomas
Flores, Cecilia
Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents
title Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents
title_full Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents
title_fullStr Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents
title_full_unstemmed Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents
title_short Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents
title_sort peri-pubertal emergence of unc-5 homologue expression by dopamine neurons in rodents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900213/
https://www.ncbi.nlm.nih.gov/pubmed/20628609
http://dx.doi.org/10.1371/journal.pone.0011463
work_keys_str_mv AT manittcolleen peripubertalemergenceofunc5homologueexpressionbydopamineneuronsinrodents
AT labelledumaiscassandre peripubertalemergenceofunc5homologueexpressionbydopamineneuronsinrodents
AT engconrad peripubertalemergenceofunc5homologueexpressionbydopamineneuronsinrodents
AT grantalanna peripubertalemergenceofunc5homologueexpressionbydopamineneuronsinrodents
AT mimeeandrea peripubertalemergenceofunc5homologueexpressionbydopamineneuronsinrodents
AT strohthomas peripubertalemergenceofunc5homologueexpressionbydopamineneuronsinrodents
AT florescecilia peripubertalemergenceofunc5homologueexpressionbydopamineneuronsinrodents