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Leptin potentiates astrogenesis in the developing hypothalamus

BACKGROUND: The proper establishment of hypothalamic feeding circuits during early development has a profound influence on energy homeostasis, and perturbing this process could predispose individuals to obesity and its associated consequences later in life. The maturation of hypothalamic neuronal ci...

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Autores principales: Rottkamp, Daniele M., Rudenko, Ivan A., Maier, Matthew T., Roshanbin, Sahar, Yulyaningsih, Ernie, Perez, Luz, Valdearcos, Martin, Chua, Streamson, Koliwad, Suneil K., Xu, Allison W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632125/
https://www.ncbi.nlm.nih.gov/pubmed/26629411
http://dx.doi.org/10.1016/j.molmet.2015.08.005
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author Rottkamp, Daniele M.
Rudenko, Ivan A.
Maier, Matthew T.
Roshanbin, Sahar
Yulyaningsih, Ernie
Perez, Luz
Valdearcos, Martin
Chua, Streamson
Koliwad, Suneil K.
Xu, Allison W.
author_facet Rottkamp, Daniele M.
Rudenko, Ivan A.
Maier, Matthew T.
Roshanbin, Sahar
Yulyaningsih, Ernie
Perez, Luz
Valdearcos, Martin
Chua, Streamson
Koliwad, Suneil K.
Xu, Allison W.
author_sort Rottkamp, Daniele M.
collection PubMed
description BACKGROUND: The proper establishment of hypothalamic feeding circuits during early development has a profound influence on energy homeostasis, and perturbing this process could predispose individuals to obesity and its associated consequences later in life. The maturation of hypothalamic neuronal circuitry in rodents takes place during the initial postnatal weeks, and this coincides with a dramatic surge in the circulating level of leptin, which is known to regulate the outgrowth of key neuronal projections in the maturing hypothalamus. Coincidently, this early postnatal period also marks the rapid proliferation and expansion of astrocytes in the brain. METHODS: Here we examined the effects of leptin on the proliferative capacity of astrocytes in the developing hypothalamus by treating postnatal mice with leptin. Mutant mice were also generated to conditionally remove leptin receptors from glial fibrillary acidic protein (GFAP)-expressing cells in the postnatal period. RESULTS AND CONCLUSIONS: We show that GFAP-expressing cells in the periventricular zone of the 3rd ventricle were responsive to leptin during the initial postnatal week. Leptin enhanced the proliferation of astrocytes in the postnatal hypothalamus and conditional removal of leptin receptors from GFAP-expressing cells during early postnatal period limited astrocyte proliferation. While increasing evidence demonstrates a direct role of leptin in regulating astrocytes in the adult brain, and given the essential function of astrocytes in modulating neuronal function and connectivity, our study indicates that leptin may exert its metabolic effects, in part, by promoting hypothalamic astrogenesis during early postnatal development.
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spelling pubmed-46321252015-12-01 Leptin potentiates astrogenesis in the developing hypothalamus Rottkamp, Daniele M. Rudenko, Ivan A. Maier, Matthew T. Roshanbin, Sahar Yulyaningsih, Ernie Perez, Luz Valdearcos, Martin Chua, Streamson Koliwad, Suneil K. Xu, Allison W. Mol Metab Brief Communication BACKGROUND: The proper establishment of hypothalamic feeding circuits during early development has a profound influence on energy homeostasis, and perturbing this process could predispose individuals to obesity and its associated consequences later in life. The maturation of hypothalamic neuronal circuitry in rodents takes place during the initial postnatal weeks, and this coincides with a dramatic surge in the circulating level of leptin, which is known to regulate the outgrowth of key neuronal projections in the maturing hypothalamus. Coincidently, this early postnatal period also marks the rapid proliferation and expansion of astrocytes in the brain. METHODS: Here we examined the effects of leptin on the proliferative capacity of astrocytes in the developing hypothalamus by treating postnatal mice with leptin. Mutant mice were also generated to conditionally remove leptin receptors from glial fibrillary acidic protein (GFAP)-expressing cells in the postnatal period. RESULTS AND CONCLUSIONS: We show that GFAP-expressing cells in the periventricular zone of the 3rd ventricle were responsive to leptin during the initial postnatal week. Leptin enhanced the proliferation of astrocytes in the postnatal hypothalamus and conditional removal of leptin receptors from GFAP-expressing cells during early postnatal period limited astrocyte proliferation. While increasing evidence demonstrates a direct role of leptin in regulating astrocytes in the adult brain, and given the essential function of astrocytes in modulating neuronal function and connectivity, our study indicates that leptin may exert its metabolic effects, in part, by promoting hypothalamic astrogenesis during early postnatal development. Elsevier 2015-09-04 /pmc/articles/PMC4632125/ /pubmed/26629411 http://dx.doi.org/10.1016/j.molmet.2015.08.005 Text en © 2015 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 Brief Communication
Rottkamp, Daniele M.
Rudenko, Ivan A.
Maier, Matthew T.
Roshanbin, Sahar
Yulyaningsih, Ernie
Perez, Luz
Valdearcos, Martin
Chua, Streamson
Koliwad, Suneil K.
Xu, Allison W.
Leptin potentiates astrogenesis in the developing hypothalamus
title Leptin potentiates astrogenesis in the developing hypothalamus
title_full Leptin potentiates astrogenesis in the developing hypothalamus
title_fullStr Leptin potentiates astrogenesis in the developing hypothalamus
title_full_unstemmed Leptin potentiates astrogenesis in the developing hypothalamus
title_short Leptin potentiates astrogenesis in the developing hypothalamus
title_sort leptin potentiates astrogenesis in the developing hypothalamus
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632125/
https://www.ncbi.nlm.nih.gov/pubmed/26629411
http://dx.doi.org/10.1016/j.molmet.2015.08.005
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