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Metabolic alterations in Parkinson’s disease astrocytes

In Parkinson`s disease (PD), the loss of dopaminergic (DA) neurons in the substantia nigra pars compacta is associated with Lewy bodies arising from the accumulation of alpha-synuclein protein which leads ultimately to movement impairment. While PD has been considered a disease of the DA neurons, a...

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Autores principales: Sonninen, Tuuli-Maria, Hämäläinen, Riikka H., Koskuvi, Marja, Oksanen, Minna, Shakirzyanova, Anastasia, Wojciechowski, Sara, Puttonen, Katja, Naumenko, Nikolay, Goldsteins, Gundars, Laham-Karam, Nihay, Lehtonen, Marko, Tavi, Pasi, Koistinaho, Jari, Lehtonen, Šárka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468111/
https://www.ncbi.nlm.nih.gov/pubmed/32879386
http://dx.doi.org/10.1038/s41598-020-71329-8
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author Sonninen, Tuuli-Maria
Hämäläinen, Riikka H.
Koskuvi, Marja
Oksanen, Minna
Shakirzyanova, Anastasia
Wojciechowski, Sara
Puttonen, Katja
Naumenko, Nikolay
Goldsteins, Gundars
Laham-Karam, Nihay
Lehtonen, Marko
Tavi, Pasi
Koistinaho, Jari
Lehtonen, Šárka
author_facet Sonninen, Tuuli-Maria
Hämäläinen, Riikka H.
Koskuvi, Marja
Oksanen, Minna
Shakirzyanova, Anastasia
Wojciechowski, Sara
Puttonen, Katja
Naumenko, Nikolay
Goldsteins, Gundars
Laham-Karam, Nihay
Lehtonen, Marko
Tavi, Pasi
Koistinaho, Jari
Lehtonen, Šárka
author_sort Sonninen, Tuuli-Maria
collection PubMed
description In Parkinson`s disease (PD), the loss of dopaminergic (DA) neurons in the substantia nigra pars compacta is associated with Lewy bodies arising from the accumulation of alpha-synuclein protein which leads ultimately to movement impairment. While PD has been considered a disease of the DA neurons, a glial contribution, in particular that of astrocytes, in PD pathogenesis is starting to be uncovered. Here, we report findings from astrocytes derived from induced pluripotent stem cells of LRRK2 G2019S mutant patients, with one patient also carrying a GBA N370S mutation, as well as healthy individuals. The PD patient astrocytes manifest the hallmarks of the disease pathology including increased expression of alpha-synuclein. This has detrimental consequences, resulting in altered metabolism, disturbed Ca(2+) homeostasis and increased release of cytokines upon inflammatory stimulation. Furthermore, PD astroglial cells manifest increased levels of polyamines and polyamine precursors while lysophosphatidylethanolamine levels are decreased, both of these changes have been reported also in PD brain. Collectively, these data reveal an important role for astrocytes in PD pathology and highlight the potential of iPSC-derived cells in disease modeling and drug discovery.
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spelling pubmed-74681112020-09-03 Metabolic alterations in Parkinson’s disease astrocytes Sonninen, Tuuli-Maria Hämäläinen, Riikka H. Koskuvi, Marja Oksanen, Minna Shakirzyanova, Anastasia Wojciechowski, Sara Puttonen, Katja Naumenko, Nikolay Goldsteins, Gundars Laham-Karam, Nihay Lehtonen, Marko Tavi, Pasi Koistinaho, Jari Lehtonen, Šárka Sci Rep Article In Parkinson`s disease (PD), the loss of dopaminergic (DA) neurons in the substantia nigra pars compacta is associated with Lewy bodies arising from the accumulation of alpha-synuclein protein which leads ultimately to movement impairment. While PD has been considered a disease of the DA neurons, a glial contribution, in particular that of astrocytes, in PD pathogenesis is starting to be uncovered. Here, we report findings from astrocytes derived from induced pluripotent stem cells of LRRK2 G2019S mutant patients, with one patient also carrying a GBA N370S mutation, as well as healthy individuals. The PD patient astrocytes manifest the hallmarks of the disease pathology including increased expression of alpha-synuclein. This has detrimental consequences, resulting in altered metabolism, disturbed Ca(2+) homeostasis and increased release of cytokines upon inflammatory stimulation. Furthermore, PD astroglial cells manifest increased levels of polyamines and polyamine precursors while lysophosphatidylethanolamine levels are decreased, both of these changes have been reported also in PD brain. Collectively, these data reveal an important role for astrocytes in PD pathology and highlight the potential of iPSC-derived cells in disease modeling and drug discovery. Nature Publishing Group UK 2020-09-02 /pmc/articles/PMC7468111/ /pubmed/32879386 http://dx.doi.org/10.1038/s41598-020-71329-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sonninen, Tuuli-Maria
Hämäläinen, Riikka H.
Koskuvi, Marja
Oksanen, Minna
Shakirzyanova, Anastasia
Wojciechowski, Sara
Puttonen, Katja
Naumenko, Nikolay
Goldsteins, Gundars
Laham-Karam, Nihay
Lehtonen, Marko
Tavi, Pasi
Koistinaho, Jari
Lehtonen, Šárka
Metabolic alterations in Parkinson’s disease astrocytes
title Metabolic alterations in Parkinson’s disease astrocytes
title_full Metabolic alterations in Parkinson’s disease astrocytes
title_fullStr Metabolic alterations in Parkinson’s disease astrocytes
title_full_unstemmed Metabolic alterations in Parkinson’s disease astrocytes
title_short Metabolic alterations in Parkinson’s disease astrocytes
title_sort metabolic alterations in parkinson’s disease astrocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468111/
https://www.ncbi.nlm.nih.gov/pubmed/32879386
http://dx.doi.org/10.1038/s41598-020-71329-8
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