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Hunot, S.

Publications and source records attributed to Hunot, S..

2 recordsLinked to original sources

Microglial Foxo3 shapes dopaminergic vulnerability in Parkinson disease

Neurodegenerative diseases such as Parkinsons disease (PD) result from complex interactions between neuronal stress and the surrounding tissue environment, yet the determinants that govern this interplay remain incompletely understood. While neuronal responses to mitochondrial dysfunction and proteotoxic stress have been extensively characterized, the contribution of the microglial state to disease progression remains unclear. Here, we identify the transcription factor Foxo3 as a key regulator of dopaminergic vulnerability acting predominantly through microglia-, rather than neuron-intrinsic, mechanisms. Foxo3 was rapidly induced and translocated to the nucleus in dopaminergic-like cells in response to mitochondrial complex I inhibition and -synuclein aggregation, indicating activation of a conserved neuronal stress response. However, neuron-specific deletion of Foxo3 attenuated early Parkinson-like transcriptional signatures but did not confer sustained in vivo neuroprotection. In contrast, microglia-specific deletion of Foxo3 provided robust and durable protection against dopaminergic degeneration across complementary mouse models, including both MPTP intoxication and -synuclein-driven pathology. Translatomic profiling revealed that Foxo3 deficiency induces extensive transcriptional remodeling of microglia at baseline, establishing a distinct state enriched in immune-related and phagocytic pathways that remains compatible with tissue homeostasis. Strikingly, neuroprotection occurred despite minimal transcriptional reprogramming following neurotoxic insult, suggesting that disease outcome is dictated by the baseline microglial state rather than by the magnitude of transcriptional responses to neurotoxic insult. Mechanistically, neuroprotection correlated with selective modulation of discrete signaling nodes, including reinforcement of the TREM2-TYROBP axis and attenuation of pathways involved in intracellular signal amplification, rather than with broad suppression of inflammatory programs. These findings indicate that Foxo3 does not primarily regulate the magnitude of microglial activation, but instead defines the baseline configuration and response thresholds that shape subsequent neuroimmune dynamics. Together, our results identify baseline microglial state as a determinant of neurodegenerative trajectory and position Foxo3 as a central regulator of this process. More broadly, these findings provide a framework in which microglial state-setting, rather than the magnitude of reactive responses alone, governs dopaminergic vulnerability, with potential implications for therapeutic strategies targeting neuroimmune interactions in Parkinsons disease.

neuroscience↗

Parkinson's disease-derived alpha-Synuclein assemblies combined with TNFalpha and Prostaglandin E2 induces a specific chronic-type inflammatory phenotype in microglial cells

Parkinsons disease (PD) is a common age-related neurodegenerative disorder characterized by the aggregation of -synuclein (SYN) building up intraneuronal inclusions termed Lewy pathology. Mounting evidence suggests that neuron-released SYN aggregates could be central to microglial activation, which in turn mounts and orchestrates neuroinflammatory processes potentially harmful to neurons. Therefore, understanding the mechanisms that drive microglial cell activation, polarization and function in PD might have important therapeutic implications. Here, using primary microglia, we investigated the inflammatory potential of pure SYN fibrils derived from PD patients. We further explored and characterized microglial cell responses to a chronic-type inflammatory stimulation combining PD patient-derived SYN fibrils (FPD), Tumor necrosis factor- (TNF) and prostaglandin E2 (PGE2) (TPFPD). We showed that FPD hold stronger inflammatory potency than pure SYN fibrils generated de novo. When combined with TNF and PGE2, FPD polarizes microglia toward a particular functional phenotype departing from FPD-treated cells and featuring lower inflammatory cytokine and higher glutamate release. Whereas metabolomic studies showed that TPFPD-exposed microglia were closely related to classically activated M1 proinflammatory cells, notably with similar tricarboxylic acid cycle disruption, transcriptomic analysis revealed that TPFPD-activated microglia assume a unique molecular signature highlighting upregulation of genes involved in glutathione and iron metabolisms. In particular, TPFPD-specific upregulation of Slc7a11 (which encodes the cystine-glutamate antiporter xCT) was consistent with the increased glutamate response and cytotoxic activity of these cells toward midbrain dopaminergic neurons in vitro. Together, these data further extend the structure-pathological relationship of SYN fibrillar polymorphs to their innate immune properties and demonstrate that PD-derived SYN fibrils, TNF and PGE2 act in concert to drive microglial cell activation toward a specific and highly neurotoxic chronic-type inflammatory phenotype characterized by robust glutamate release and iron retention.

neuroscience↗