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...
Autores principales: | , , , , , , |
---|---|
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 |