Leptin receptor-positive and leptin receptor-negative proopiomelanocortin neurons innervate an identical set of brain structures

Leandro B Lima, Martin Metzger, Isadora C Furigo, J Donato

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

Neurons that express the prohormone proopiomelanocortin (POMC) in the arcuate hypothalamic nucleus (Arc) are engaged in the regulation of energy balance and glucose homeostasis. Additionally, POMC neurons are considered key first-order cells regulated by leptin. Interestingly, in the Arc, POMC cells that express the leptin receptor (POMC/LepR+ cells) are found side by side with POMC cells not directly responsive to leptin (POMC/LepR- cells). However, it remains unknown whether these distinct populations innervate different target regions. Therefore, the objective of the present study was to compare the projections of POMC/LepR+ and POMC/LepR- neurons. Using genetically modified LepR-reporter mice to identify leptin receptor-expressing cells and immunohistochemistry to stain POMC-derived peptides (α-MSH or β-endorphin) we confirmed that approximately 80% of Arc β-endorphin-positive neurons co-expressed leptin receptors. POMC/LepR+ and POMC/LepR- axons were intermingled in all of their target regions. As revealed by confocal microscopy, we found an elevated degree of co-localization between α-MSH+ axons and the reporter protein (tdTomato) in all brain regions analyzed, with co-localization coefficients ranging from 0.889 to 0.701. Thus, these two populations of POMC neurons seem to project to the same set of brain structures, although one of the two subtypes of POMC axons was sometimes found to be more abundant than the other in distinct subregions of the same nucleus. Therefore, POMC/LepR+ and POMC/LepR- cells may target separate neuronal populations and consequently activate distinct neuronal circuits within some target nuclei. These findings contribute to unravel the neuronal circuits involved in the regulation of energy balance and glucose homeostasis.

Original languageEnglish
Pages (from-to)366-376
Number of pages11
JournalBrain Research
Volume1646
Early online date16 Jun 2016
DOIs
Publication statusPublished - 1 Sept 2016
Externally publishedYes

Bibliographical note

Copyright © 2016 Elsevier B.V. All rights reserved.

Funder

São Paulo Research Foundation (FAPESP-Brazil, Grant numbers: 2010/18086-0, 2012/02388-3 and 2015/10992-6)

Keywords

  • POMC
  • α-MSH
  • β-endorphin
  • Melanocortin
  • ROSA26 Cre reporter
  • Hypothalamus

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