TSPO contributes to neuropathology and cognitive deficits in Alzheimer’s disease

The 18kDa translocator protein (TSPO) is increased in neurodegenerative diseases. In Alzheimer's disease (AD) animal models, TSPO's upregulation is detected first in astrocytes, then in microglia. However, the role of TSPO in the pathophysiology and symptoms characteristic of the disease remains unknown. In the human postmortem hippocampus, we show here that TSPO correlated positively with reactive astrocyte-associated genes and negatively with genes involved in glycolytic pathways. In addition, we observed that TSPO deletion in 3 × TgAD mice reversed the reduction in glucose uptake and reduced astrocyte reactivity. We observed a decrease of poorly and highly aggregated forms of Tau (-44% and -82%, respectively) and Aβ42 (-25% and -95%, respectively) at 9 months of age. In 5 × FAD mice, we confirmed the association between TSPO, astrocyte reactivity and Aβ. Functionally, Tau over-expression in the hippocampus induced a memory decline in WT animals, prevented in TSPO<sup>-/-</sup> mice. Altogether, these data demonstrate that TSPO plays an important role in the active progression of AD. This identifies TSPO as a potential therapeutic target and highlights the importance of astrocyte metabolism in the pathogenesis of the disease.

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Publication Details

Journal
Journal of Neuroinflammation
Published
2025-10-28
DOI
https://doi.org/10.1186/s12974-025-03583-4
Citations
4
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
4.66
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article

TSPO contributes to neuropathology and cognitive deficits in Alzheimer’s disease

Léa Meyer, Guo Jun Liu, Marta Bałkota, Pierre Maechler et al.
4 citations
Journal of Neuroinflammation
Alzheimer's disease research and treatments
4.66
article

TSPO contributes to neuropathology and cognitive deficits in Alzheimer’s disease

Léa Meyer, Guo Jun Liu, Marta Bałkota, Pierre Maechler, Richard B. Banati, Thomas Zilli, Stergios Tsartsalis, Valentina Garibotto, Ryan J. Middleton, Laurene Abjean, Farha Bouteldja, David R. Owen, Quentin Amossé, Aurélien Lathuilière, P. Millet, Benjamin B. Tournier, Kelly Ceyzériat, Aurélien M. Badina, Oriane Prudhomme
article en
4 citations

Abstract

The 18kDa translocator protein (TSPO) is increased in neurodegenerative diseases. In Alzheimer's disease (AD) animal models, TSPO's upregulation is detected first in astrocytes, then in microglia. However, the role of TSPO in the pathophysiology and symptoms characteristic of the disease remains unknown. In the human postmortem hippocampus, we show here that TSPO correlated positively with reactive astrocyte-associated genes and negatively with genes involved in glycolytic pathways. In addition, we observed that TSPO deletion in 3 × TgAD mice reversed the reduction in glucose uptake and reduced astrocyte reactivity. We observed a decrease of poorly and highly aggregated forms of Tau (-44% and -82%, respectively) and Aβ42 (-25% and -95%, respectively) at 9 months of age. In 5 × FAD mice, we confirmed the association between TSPO, astrocyte reactivity and Aβ. Functionally, Tau over-expression in the hippocampus induced a memory decline in WT animals, prevented in TSPO<sup>-/-</sup> mice. Altogether, these data demonstrate that TSPO plays an important role in the active progression of AD. This identifies TSPO as a potential therapeutic target and highlights the importance of astrocyte metabolism in the pathogenesis of the disease.

Journal of NeuroinflammationVol. 22(1)
University of Geneva (CH), The University of Sydney (AU), Australian Nuclear Science and Technology Organisation (AU), Institute of Oncology Research (CH), University Hospital of Geneva (CH), UK Dementia Research Institute (GB), Centre d'Imagerie BioMedicale (CH), Imperial College London (GB), Università della Svizzera italiana (CH), Geneva College (US)
Openalex Percentile: Top 5%
Alzheimer's disease research and treatments
4.66
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