Inactivation of the PHD3-FOXO3 axis blunts the type I interferon response in microglia and ameliorates Alzheimer’s disease progression

Microglia respond to Alzheimer's disease (AD) with varied transcriptional responses. We show that oligomeric Aß (oAß) induces the expression of <i>Hif1a</i> and <i>Egln3</i> in microglia in vitro, together with the transcription of the type I interferon signature (IFNS) genes in a PHD3-dependent manner. We identify FOXO3 as a repressor of IFNS, whose abundance decreases upon PHD3 induction in response to oAß. In vivo, loss of PHD3 correlates with abrogation of the IFNS and activation of the disease-associated microglia signature, an increase in microglia proximity to Aß plaques and phagocytosis of both Aß and small plaques. PHD3 deficiency mitigated the Aß plaque-associated neuropathology and rescued behavioral deficits of an AD mouse model. Last, we demonstrate that microglial PHD3 overexpression in the absence of Aß pathology is sufficient to induce the IFNS and behavioral alterations. Together, our data strongly indicate that the inactivation of the PHD3-FOXO3 axis controls the microglial IFNS in a cell autonomous manner, improving AD outcome.

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Publication Details

Journal
Science Advances
Published
2025-05-28
DOI
https://doi.org/10.1126/sciadv.adu2244
Citations
4
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
3.37
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article

Inactivation of the PHD3-FOXO3 axis blunts the type I interferon response in microglia and ameliorates Alzheimer’s disease progression

Carmen Romero‐Molina, Rosana March‐Díaz, Alberto Pascual, Manuel A. Sánchez-García et al.
4 citations
Science Advances
Neuroinflammation and Neurodegeneration Mechanisms
3.37
article

Inactivation of the PHD3-FOXO3 axis blunts the type I interferon response in microglia and ameliorates Alzheimer’s disease progression

Carmen Romero‐Molina, Rosana March‐Díaz, Alberto Pascual, Manuel A. Sánchez-García, Victoria Navarro, Marisa Vizuete, Daniel Cabello-Rivera, Ana M. Muñoz-Cabello, Juan M. Barba-Reyes, Alicia E. Rosales‐Nieves, Javier Vitórica, Clara Ortega‐de San Luis, Matthew E. Cockman, Antonio Heras‐Garvin, José López‐Barneo, Ana B. Muñoz‐Manchado, Nieves Lara-Ureña, Silvia Quiñones-Cañete, Bella Mora-Romero
article en
4 citations

Abstract

Microglia respond to Alzheimer's disease (AD) with varied transcriptional responses. We show that oligomeric Aß (oAß) induces the expression of <i>Hif1a</i> and <i>Egln3</i> in microglia in vitro, together with the transcription of the type I interferon signature (IFNS) genes in a PHD3-dependent manner. We identify FOXO3 as a repressor of IFNS, whose abundance decreases upon PHD3 induction in response to oAß. In vivo, loss of PHD3 correlates with abrogation of the IFNS and activation of the disease-associated microglia signature, an increase in microglia proximity to Aß plaques and phagocytosis of both Aß and small plaques. PHD3 deficiency mitigated the Aß plaque-associated neuropathology and rescued behavioral deficits of an AD mouse model. Last, we demonstrate that microglial PHD3 overexpression in the absence of Aß pathology is sufficient to induce the IFNS and behavioral alterations. Together, our data strongly indicate that the inactivation of the PHD3-FOXO3 axis controls the microglial IFNS in a cell autonomous manner, improving AD outcome.

Science AdvancesVol. 11(22)
The Francis Crick Institute (GB), Instituto de Salud Carlos III (ES), Karolinska Institutet (SE), Biomedical Research Networking Center on Neurodegenerative Diseases (ES), Centro de Investigación Biomédica en Red de Salud Mental (ES), Biomedical Research and Innovation Institute of Cadiz (ES), Instituto de Biomedicina de Sevilla (ES), Hospital Universitario Virgen del Rocío (ES), Universidad de Sevilla (ES)
Good health and well-being
Openalex Percentile: Top 8%
Neuroinflammation and Neurodegeneration Mechanisms
3.37
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