Abstract
Converging evidence made clear that declining brain energetics contribute to aging and are implicated in the initiation and progression of neurodegenerative disorders such as Alzheimer’s and Parkinson’s disease. Indeed, both pathologies involve instances of hypometabolism of glucose and oxygen in the brain causing mitochondrial dysfunction, energetic failure and oxidative stress. Importantly, recent evidence suggests that astrocytes, which play a key role in supporting neuronal function and metabolism, might contribute to the development of neurodegenerative diseases. Therefore, exploring how the neuro-supportive role of astrocytes may be impaired in the context of these disorders has great therapeutic potential. In the following, we will discuss some of the so far identified features underlining the astrocyte-neuron metabolic crosstalk. Thereby, special focus will be given to the role of mitochondria. Furthermore, we will report on recent advancements concerning iPSC-derived models used to unravel the metabolic contribution of astrocytes to neuronal demise. Finally, we discuss how mitochondrial dysfunction in astrocytes could contribute to inflammatory signaling in neurodegenerative diseases.
| Original language | English |
|---|---|
| Article number | 668517 |
| Journal | Frontiers in Endocrinology |
| Volume | 12 |
| Pages (from-to) | 668517 |
| ISSN | 1664-2392 |
| DOIs | |
| Publication status | Published - 07.05.2021 |
Funding
PM, SP, and AG were supported by the Luxembourg National Research Fund (FNR) within the CORE (CAMeSyn, C19/BM/ 13688526) and ATTRACT programs (Model-IPD, FNR9631103). In addition, PM was supported by the FNR via the PARK-QC DTU (PRIDE17/12244779/PARK-QC). AG and SP were supported by a donation from Le Foyer Assurances Luxembourg, which was matched by the FNR within the framework of the PARK-QC DTU program.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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SDG 10 Reduced Inequalities
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