Amylin Selectively Signals Onto POMC Neurons in the Arcuate Nucleus of the Hypothalamus

Amylin phosphorylates ERK (p-ERK) in the area postrema to reduce eating and synergizes with leptin to phosphorylate STAT3 in the arcuate (ARC) and ventromedial (VMN) hypothalamic nuclei to reduce food intake and body weight. The current studies assessed potential amylin and amylin-leptin ARC/VMN int...

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Published inDiabetes (New York, N.Y.) Vol. 67; no. 5; pp. 805 - 817
Main Authors Lutz, Thomas A., Coester, Bernd, Whiting, Lynda, Dunn-Meynell, Ambrose A., Boyle, Christina N., Bouret, Sebastien G., Levin, Barry E., Le Foll, Christelle
Format Journal Article
LanguageEnglish
Published United States American Diabetes Association 01.05.2018
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Online AccessGet full text
ISSN0012-1797
1939-327X
1939-327X
DOI10.2337/db17-1347

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Abstract Amylin phosphorylates ERK (p-ERK) in the area postrema to reduce eating and synergizes with leptin to phosphorylate STAT3 in the arcuate (ARC) and ventromedial (VMN) hypothalamic nuclei to reduce food intake and body weight. The current studies assessed potential amylin and amylin-leptin ARC/VMN interactions on ERK signaling and their roles in postnatal hypothalamic pathway development. In amylin knockout mice, the density of agouti-related protein (AgRP)-immunoreactive (IR) fibers in the hypothalamic paraventricular nucleus (PVN) was increased, while the density of α-melanocyte–stimulating hormone (αMSH) fibers was decreased. In mice deficient of the amylin receptor components RAMP1/3, both AgRP and αMSH-IR fiber densities were decreased, while only αMSH-IR fiber density was decreased in rats injected neonatally in the ARC/VMN with an adeno-associated virus short hairpin RNA against the amylin core receptor. Amylin induced p-ERK in ARC neurons, 60% of which was present in POMC-expressing neurons, with none in NPY neurons. An amylin-leptin interaction was shown by an additive effect on ARC ERK signaling in neonatal rats and a 44% decrease in amylin-induced p-ERK in the ARC of leptin receptor–deficient and of ob/ob mice. Together, these results suggest that amylin directly acts, through a p-ERK–mediated process, on POMC neurons to enhance ARC-PVN αMSH pathway development.
AbstractList Amylin phosphorylates ERK (p-ERK) in the area postrema to reduce eating and synergizes with leptin to phosphorylate STAT3 in the arcuate (ARC) and ventromedial (VMN) hypothalamic nuclei to reduce food intake and body weight. The current studies assessed potential amylin and amylin-leptin ARC/VMN interactions on ERK signaling and their roles in postnatal hypothalamic pathway development. In amylin knockout mice, the density of agouti-related protein (AgRP)-immunoreactive (IR) fibers in the hypothalamic paraventricular nucleus (PVN) was increased, while the density of α-melanocyte–stimulating hormone (αMSH) fibers was decreased. In mice deficient of the amylin receptor components RAMP1/3, both AgRP and αMSH-IR fiber densities were decreased, while only αMSH-IR fiber density was decreased in rats injected neonatally in the ARC/VMN with an adeno-associated virus short hairpin RNA against the amylin core receptor. Amylin induced p-ERK in ARC neurons, 60% of which was present in POMC-expressing neurons, with none in NPY neurons. An amylin-leptin interaction was shown by an additive effect on ARC ERK signaling in neonatal rats and a 44% decrease in amylin-induced p-ERK in the ARC of leptin receptor–deficient and of ob/ob mice. Together, these results suggest that amylin directly acts, through a p-ERK–mediated process, on POMC neurons to enhance ARC-PVN αMSH pathway development.
Amylin phosphorylates ERK (p-ERK) in the area postrema to reduce eating and synergizes with leptin to phosphorylate STAT3 in the arcuate (ARC) and ventromedial (VMN) hypothalamic nuclei to reduce food intake and body weight. The current studies assessed potential amylin and amylin-leptin ARC/VMN interactions on ERK signaling and their roles in postnatal hypothalamic pathway development. In amylin knockout mice, the density of agouti-related protein (AgRP)-immunoreactive (IR) fibers in the hypothalamic paraventricular nucleus (PVN) was increased, while the density of α-melanocyte-stimulating hormone (αMSH) fibers was decreased. In mice deficient of the amylin receptor components RAMP1/3, both AgRP and αMSH-IR fiber densities were decreased, while only αMSH-IR fiber density was decreased in rats injected neonatally in the ARC/VMN with an adeno-associated virus short hairpin RNA against the amylin core receptor. Amylin induced p-ERK in ARC neurons, 60% of which was present in POMC-expressing neurons, with none in NPY neurons. An amylin-leptin interaction was shown by an additive effect on ARC ERK signaling in neonatal rats and a 44% decrease in amylin-induced p-ERK in the ARC of leptin receptor-deficient and of ob/ob mice. Together, these results suggest that amylin directly acts, through a p-ERK-mediated process, on POMC neurons to enhance ARC-PVN αMSH pathway development.Amylin phosphorylates ERK (p-ERK) in the area postrema to reduce eating and synergizes with leptin to phosphorylate STAT3 in the arcuate (ARC) and ventromedial (VMN) hypothalamic nuclei to reduce food intake and body weight. The current studies assessed potential amylin and amylin-leptin ARC/VMN interactions on ERK signaling and their roles in postnatal hypothalamic pathway development. In amylin knockout mice, the density of agouti-related protein (AgRP)-immunoreactive (IR) fibers in the hypothalamic paraventricular nucleus (PVN) was increased, while the density of α-melanocyte-stimulating hormone (αMSH) fibers was decreased. In mice deficient of the amylin receptor components RAMP1/3, both AgRP and αMSH-IR fiber densities were decreased, while only αMSH-IR fiber density was decreased in rats injected neonatally in the ARC/VMN with an adeno-associated virus short hairpin RNA against the amylin core receptor. Amylin induced p-ERK in ARC neurons, 60% of which was present in POMC-expressing neurons, with none in NPY neurons. An amylin-leptin interaction was shown by an additive effect on ARC ERK signaling in neonatal rats and a 44% decrease in amylin-induced p-ERK in the ARC of leptin receptor-deficient and of ob/ob mice. Together, these results suggest that amylin directly acts, through a p-ERK-mediated process, on POMC neurons to enhance ARC-PVN αMSH pathway development.
Author Coester, Bernd
Lutz, Thomas A.
Le Foll, Christelle
Whiting, Lynda
Boyle, Christina N.
Dunn-Meynell, Ambrose A.
Levin, Barry E.
Bouret, Sebastien G.
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  orcidid: 0000-0002-6677-5488
  surname: Le Foll
  fullname: Le Foll, Christelle
  organization: Institute of Veterinary Physiology, University of Zurich, Zurich, Switzerland
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Snippet Amylin phosphorylates ERK (p-ERK) in the area postrema to reduce eating and synergizes with leptin to phosphorylate STAT3 in the arcuate (ARC) and ventromedial...
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SubjectTerms Agouti-related protein
Agouti-Related Protein - metabolism
alpha-MSH - metabolism
Amylin
Animal models
Animals
Animals, Newborn
Arcuate nucleus
Arcuate Nucleus of Hypothalamus - metabolism
Area postrema
Body weight
Diabetes
Feeding Behavior
Female
Fibers
Food intake
Health care
Hypothalamus
Islet Amyloid Polypeptide - genetics
Islet Amyloid Polypeptide - metabolism
Leptin - metabolism
Male
MAP Kinase Signaling System
Metabolism
Mice
Mice, Knockout
Mice, Obese
Neonates
Neurons
Neurons - metabolism
Neuropeptide Y
Neuropeptide Y - metabolism
Paraventricular Hypothalamic Nucleus - metabolism
Paraventricular nucleus
Pro-Opiomelanocortin - metabolism
Proopiomelanocortin
Rats, Sprague-Dawley
Receptor activity modifying proteins
Receptor Activity-Modifying Protein 1 - genetics
Receptor Activity-Modifying Protein 1 - metabolism
Receptor Activity-Modifying Protein 3 - genetics
Receptor Activity-Modifying Protein 3 - metabolism
Ribonucleic acid
RNA
RNA viruses
Signal transduction
Stat3 protein
Ventromedial Hypothalamic Nucleus - metabolism
Title Amylin Selectively Signals Onto POMC Neurons in the Arcuate Nucleus of the Hypothalamus
URI https://www.ncbi.nlm.nih.gov/pubmed/29467172
https://www.proquest.com/docview/2090480979
https://www.proquest.com/docview/2007420108
https://pubmed.ncbi.nlm.nih.gov/PMC5910000
Volume 67
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