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Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship

A brain clock, constituted of ∼20,000 peptidergically heterogeneous neurons, is located in the hypothalamic suprachiasmatic nucleus (SCN). While many peptidergic cell types have been identified, little is known about the connections among these neurons in mice. We first sought to identify contacts a...

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Autores principales: Varadarajan, Shruti, Tajiri, Mary, Jain, Rashi, Holt, Rebecca, Ahmed, Qanetha, LeSauter, Joseph, Silver, Rae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168316/
https://www.ncbi.nlm.nih.gov/pubmed/30283813
http://dx.doi.org/10.1523/ENEURO.0205-18.2018
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author Varadarajan, Shruti
Tajiri, Mary
Jain, Rashi
Holt, Rebecca
Ahmed, Qanetha
LeSauter, Joseph
Silver, Rae
author_facet Varadarajan, Shruti
Tajiri, Mary
Jain, Rashi
Holt, Rebecca
Ahmed, Qanetha
LeSauter, Joseph
Silver, Rae
author_sort Varadarajan, Shruti
collection PubMed
description A brain clock, constituted of ∼20,000 peptidergically heterogeneous neurons, is located in the hypothalamic suprachiasmatic nucleus (SCN). While many peptidergic cell types have been identified, little is known about the connections among these neurons in mice. We first sought to identify contacts among major peptidergic cell types in the SCN using triple-label fluorescent immunocytochemistry (ICC). To this end, contacts among vasoactive intestinal polypeptide (VIP), gastrin-releasing peptide (GRP), and calretinin (CALR) cells of the core, and arginine vasopressin (AVP) and met-enkephalin (ENK) cells of the shell were analyzed. Some core-to-shell and shell-to-core communications are specialized. We found that in wild-type (WT) mice, AVP fibers make extremely sparse contacts onto VIP neurons but contacts in the reverse direction are numerous. In contrast, AVP fibers make more contacts onto GRP neurons than conversely. For the other cell types tested, largely reciprocal connections are made. These results point to peptidergic cell type-specific communications between core and shell SCN neurons. To further understand the impact of VIP-to-AVP communication, we next explored the SCN in VIP-deficient mice (VIP-KO). In these animals, AVP expression is markedly reduced in the SCN, but it is not altered in the paraventricular nucleus (PVN) and supraoptic nucleus (SON). Surprisingly, in VIP-KO mice, the number of AVP appositions onto other peptidergic cell types is not different from controls. Colchicine administration, which blocks AVP transport, restored the numbers of AVP neurons in VIP-KO to that of WT littermates. The results indicate that VIP has an important role in modulating AVP expression levels in the SCN in this mouse.
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spelling pubmed-61683162018-10-03 Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship Varadarajan, Shruti Tajiri, Mary Jain, Rashi Holt, Rebecca Ahmed, Qanetha LeSauter, Joseph Silver, Rae eNeuro New Research A brain clock, constituted of ∼20,000 peptidergically heterogeneous neurons, is located in the hypothalamic suprachiasmatic nucleus (SCN). While many peptidergic cell types have been identified, little is known about the connections among these neurons in mice. We first sought to identify contacts among major peptidergic cell types in the SCN using triple-label fluorescent immunocytochemistry (ICC). To this end, contacts among vasoactive intestinal polypeptide (VIP), gastrin-releasing peptide (GRP), and calretinin (CALR) cells of the core, and arginine vasopressin (AVP) and met-enkephalin (ENK) cells of the shell were analyzed. Some core-to-shell and shell-to-core communications are specialized. We found that in wild-type (WT) mice, AVP fibers make extremely sparse contacts onto VIP neurons but contacts in the reverse direction are numerous. In contrast, AVP fibers make more contacts onto GRP neurons than conversely. For the other cell types tested, largely reciprocal connections are made. These results point to peptidergic cell type-specific communications between core and shell SCN neurons. To further understand the impact of VIP-to-AVP communication, we next explored the SCN in VIP-deficient mice (VIP-KO). In these animals, AVP expression is markedly reduced in the SCN, but it is not altered in the paraventricular nucleus (PVN) and supraoptic nucleus (SON). Surprisingly, in VIP-KO mice, the number of AVP appositions onto other peptidergic cell types is not different from controls. Colchicine administration, which blocks AVP transport, restored the numbers of AVP neurons in VIP-KO to that of WT littermates. The results indicate that VIP has an important role in modulating AVP expression levels in the SCN in this mouse. Society for Neuroscience 2018-10-02 /pmc/articles/PMC6168316/ /pubmed/30283813 http://dx.doi.org/10.1523/ENEURO.0205-18.2018 Text en Copyright © 2018 Varadarajan et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Varadarajan, Shruti
Tajiri, Mary
Jain, Rashi
Holt, Rebecca
Ahmed, Qanetha
LeSauter, Joseph
Silver, Rae
Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship
title Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship
title_full Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship
title_fullStr Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship
title_full_unstemmed Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship
title_short Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship
title_sort connectome of the suprachiasmatic nucleus: new evidence of the core-shell relationship
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168316/
https://www.ncbi.nlm.nih.gov/pubmed/30283813
http://dx.doi.org/10.1523/ENEURO.0205-18.2018
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