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MCH Neurons Regulate Permeability of the Median Eminence Barrier
Melanin-concentrating hormone (MCH)-expressing neurons are key regulators of energy and glucose homeostasis. Here, we demonstrate that they provide dense projections to the median eminence (ME) in close proximity to tanycytes and fenestrated vessels. Chemogenetic activation of MCH neurons as well as...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383232/ https://www.ncbi.nlm.nih.gov/pubmed/32407670 http://dx.doi.org/10.1016/j.neuron.2020.04.020 |
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author | Jiang, Hong Gallet, Sarah Klemm, Paul Scholl, Pia Folz-Donahue, Kat Altmüller, Janine Alber, Jens Heilinger, Christian Kukat, Christian Loyens, Anne Müller-Fielitz, Helge Sundaram, Sivaraj Schwaninger, Markus Prevot, Vincent Brüning, Jens C. |
author_facet | Jiang, Hong Gallet, Sarah Klemm, Paul Scholl, Pia Folz-Donahue, Kat Altmüller, Janine Alber, Jens Heilinger, Christian Kukat, Christian Loyens, Anne Müller-Fielitz, Helge Sundaram, Sivaraj Schwaninger, Markus Prevot, Vincent Brüning, Jens C. |
author_sort | Jiang, Hong |
collection | PubMed |
description | Melanin-concentrating hormone (MCH)-expressing neurons are key regulators of energy and glucose homeostasis. Here, we demonstrate that they provide dense projections to the median eminence (ME) in close proximity to tanycytes and fenestrated vessels. Chemogenetic activation of MCH neurons as well as optogenetic stimulation of their projections in the ME enhance permeability of the ME by increasing fenestrated vascular loops and enhance leptin action in the arcuate nucleus of the hypothalamus (ARC). Unbiased phosphoRiboTrap-based assessment of cell activation upon chemogenetic MCH neuron activation reveals MCH-neuron-dependent regulation of endothelial cells. MCH neurons express the vascular endothelial growth factor A (VEGFA), and blocking VEGF-R signaling attenuates the leptin-sensitizing effect of MCH neuron activation. Our experiments reveal that MCH neurons directly regulate permeability of the ME barrier, linking the activity of energy state and sleep regulatory neurons to the regulation of hormone accessibility to the ARC. |
format | Online Article Text |
id | pubmed-7383232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73832322020-07-30 MCH Neurons Regulate Permeability of the Median Eminence Barrier Jiang, Hong Gallet, Sarah Klemm, Paul Scholl, Pia Folz-Donahue, Kat Altmüller, Janine Alber, Jens Heilinger, Christian Kukat, Christian Loyens, Anne Müller-Fielitz, Helge Sundaram, Sivaraj Schwaninger, Markus Prevot, Vincent Brüning, Jens C. Neuron Article Melanin-concentrating hormone (MCH)-expressing neurons are key regulators of energy and glucose homeostasis. Here, we demonstrate that they provide dense projections to the median eminence (ME) in close proximity to tanycytes and fenestrated vessels. Chemogenetic activation of MCH neurons as well as optogenetic stimulation of their projections in the ME enhance permeability of the ME by increasing fenestrated vascular loops and enhance leptin action in the arcuate nucleus of the hypothalamus (ARC). Unbiased phosphoRiboTrap-based assessment of cell activation upon chemogenetic MCH neuron activation reveals MCH-neuron-dependent regulation of endothelial cells. MCH neurons express the vascular endothelial growth factor A (VEGFA), and blocking VEGF-R signaling attenuates the leptin-sensitizing effect of MCH neuron activation. Our experiments reveal that MCH neurons directly regulate permeability of the ME barrier, linking the activity of energy state and sleep regulatory neurons to the regulation of hormone accessibility to the ARC. Cell Press 2020-07-22 /pmc/articles/PMC7383232/ /pubmed/32407670 http://dx.doi.org/10.1016/j.neuron.2020.04.020 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Jiang, Hong Gallet, Sarah Klemm, Paul Scholl, Pia Folz-Donahue, Kat Altmüller, Janine Alber, Jens Heilinger, Christian Kukat, Christian Loyens, Anne Müller-Fielitz, Helge Sundaram, Sivaraj Schwaninger, Markus Prevot, Vincent Brüning, Jens C. MCH Neurons Regulate Permeability of the Median Eminence Barrier |
title | MCH Neurons Regulate Permeability of the Median Eminence Barrier |
title_full | MCH Neurons Regulate Permeability of the Median Eminence Barrier |
title_fullStr | MCH Neurons Regulate Permeability of the Median Eminence Barrier |
title_full_unstemmed | MCH Neurons Regulate Permeability of the Median Eminence Barrier |
title_short | MCH Neurons Regulate Permeability of the Median Eminence Barrier |
title_sort | mch neurons regulate permeability of the median eminence barrier |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383232/ https://www.ncbi.nlm.nih.gov/pubmed/32407670 http://dx.doi.org/10.1016/j.neuron.2020.04.020 |
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