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Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes

We characterized cerebral Oil Red O-positive lipid-laden cells (LLC) of aging mice evaluating their distribution, morphology, density, functional activities and inflammatory phenotype. We identified LLC in meningeal, cortical and neurogenic brain regions. The density of cerebral LLC increased with a...

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Autores principales: Shimabukuro, Marilia Kimie, Langhi, Larissa Gutman Paranhos, Cordeiro, Ingrid, Brito, José M., Batista, Claudia Maria de Castro, Mattson, Mark P., de Mello Coelho, Valeria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814830/
https://www.ncbi.nlm.nih.gov/pubmed/27029648
http://dx.doi.org/10.1038/srep23795
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author Shimabukuro, Marilia Kimie
Langhi, Larissa Gutman Paranhos
Cordeiro, Ingrid
Brito, José M.
Batista, Claudia Maria de Castro
Mattson, Mark P.
de Mello Coelho, Valeria
author_facet Shimabukuro, Marilia Kimie
Langhi, Larissa Gutman Paranhos
Cordeiro, Ingrid
Brito, José M.
Batista, Claudia Maria de Castro
Mattson, Mark P.
de Mello Coelho, Valeria
author_sort Shimabukuro, Marilia Kimie
collection PubMed
description We characterized cerebral Oil Red O-positive lipid-laden cells (LLC) of aging mice evaluating their distribution, morphology, density, functional activities and inflammatory phenotype. We identified LLC in meningeal, cortical and neurogenic brain regions. The density of cerebral LLC increased with age. LLC presenting small lipid droplets were visualized adjacent to blood vessels or deeper in the brain cortical and striatal parenchyma of aging mice. LLC with larger droplets were asymmetrically distributed in the cerebral ventricle walls, mainly located in the lateral wall. We also found that LLC in the subventricular region co-expressed beclin-1 or LC3, markers for autophagosome or autophagolysosome formation, and perilipin (PLIN), a lipid droplet-associated protein, suggesting lipophagic activity. Some cerebral LLC exhibited β galactosidase activity indicating a senescence phenotype. Moreover, we detected production of the pro-inflammatory cytokine TNF-α in cortical PLIN(+) LLC. Some cortical NeuN(+) neurons, GFAP(+) glia limitans astrocytes, Iba-1(+) microglia and S100β(+) ependymal cells expressed PLIN in the aging brain. Our findings suggest that cerebral LLC exhibit distinct cellular phenotypes and may participate in the age-associated neuroinflammatory processes.
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spelling pubmed-48148302016-04-04 Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes Shimabukuro, Marilia Kimie Langhi, Larissa Gutman Paranhos Cordeiro, Ingrid Brito, José M. Batista, Claudia Maria de Castro Mattson, Mark P. de Mello Coelho, Valeria Sci Rep Article We characterized cerebral Oil Red O-positive lipid-laden cells (LLC) of aging mice evaluating their distribution, morphology, density, functional activities and inflammatory phenotype. We identified LLC in meningeal, cortical and neurogenic brain regions. The density of cerebral LLC increased with age. LLC presenting small lipid droplets were visualized adjacent to blood vessels or deeper in the brain cortical and striatal parenchyma of aging mice. LLC with larger droplets were asymmetrically distributed in the cerebral ventricle walls, mainly located in the lateral wall. We also found that LLC in the subventricular region co-expressed beclin-1 or LC3, markers for autophagosome or autophagolysosome formation, and perilipin (PLIN), a lipid droplet-associated protein, suggesting lipophagic activity. Some cerebral LLC exhibited β galactosidase activity indicating a senescence phenotype. Moreover, we detected production of the pro-inflammatory cytokine TNF-α in cortical PLIN(+) LLC. Some cortical NeuN(+) neurons, GFAP(+) glia limitans astrocytes, Iba-1(+) microglia and S100β(+) ependymal cells expressed PLIN in the aging brain. Our findings suggest that cerebral LLC exhibit distinct cellular phenotypes and may participate in the age-associated neuroinflammatory processes. Nature Publishing Group 2016-03-31 /pmc/articles/PMC4814830/ /pubmed/27029648 http://dx.doi.org/10.1038/srep23795 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Shimabukuro, Marilia Kimie
Langhi, Larissa Gutman Paranhos
Cordeiro, Ingrid
Brito, José M.
Batista, Claudia Maria de Castro
Mattson, Mark P.
de Mello Coelho, Valeria
Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes
title Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes
title_full Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes
title_fullStr Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes
title_full_unstemmed Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes
title_short Lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes
title_sort lipid-laden cells differentially distributed in the aging brain are functionally active and correspond to distinct phenotypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814830/
https://www.ncbi.nlm.nih.gov/pubmed/27029648
http://dx.doi.org/10.1038/srep23795
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