Protective variant in PLCgamma2 mitigates Alzheimer's disease associated pathology via enhancing beneficial microglia functions

Takalo, M.; Jeskanen, H.; Rolova, T.; Kervinen, I.; Hellen, M.; Heikkinen, S.; Koivisto, H.; Jokivarsi, K.; Muller, S. A.; Koivumaki, E.-M.; Makinen, P.; Juopperi, S.-P.; Willman, R.-M.; Sinisalo, R.; Hoffman, D.; Jantti, H.; Peitz, M.; Fliessbach, K.; Kuulasmaa, T.; Natunen, T.; Kemppainen, S.; Poutiainen, P.; Leinonen, V.; Malm, T.; Martiskainen, H.; Ramirez, A.; Haapasalo, A.; Lichtenthaler, S. F.; Tanila, H.; Haass, C.; Rinne, J.; Koistinaho, J.; Hiltunen, M.

doi:10.1101/2024.09.12.612207

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bioRxiv · 10.1101/2024.09.12.612207

Protective variant in PLCgamma2 mitigates Alzheimer's disease associated pathology via enhancing beneficial microglia functions

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Abstract

BackgroundPLC{gamma}2-P522R (phospholipase C gamma 2, proline 522 to arginine) is a protective variant that reduces the risk for late onset Alzheimers disease. Recently, it was shown to decrease {beta}-amyloid pathology in 5XFAD mouse model of AD. In this study, our goal was to investigate the protective functions of PLC{gamma}2-P522R variant in a less aggressive mouse model of AD as well as to assess the underlying mechanisms at the molecular and cellular level using mouse and human microglia models. MethodsThe effects of the protective PLC{gamma}2-P522R variant on microglia activation, AD-related {beta}-amyloid and neuronal pathologies, as well as behavioral changes were investigated in PLC{gamma}2-P522R knock-in mice crossbred with APP/PS1 AD model mice. Transcriptomic, proteomic, and functional studies were carried out in cultured and acutely isolated adult PLC{gamma}2-P522R mouse microglia to study molecular mechanisms. Finally, microglia-like cell models generated from blood and skin biopsy samples of the PLC{gamma}2-P522R variant carriers were employed to translate the key findings to human cells. ResultsOur results demonstrate that the PLC{gamma}2-P522R variant reduced brain {beta}-amyloid plaque burden of APP/PS1 mice. Simultaneously, PLC{gamma}2-P522R variant increased non-proinflammatory microglia activation and microglia clustering around {beta}-amyloid plaques, leading to reduced {beta}-amyloid plaque-associated neuronal dystrophy. In cultured mouse primary microglia, PLC{gamma}2-P522R variant decreased accumulation of large lipid droplets, reduced cell stress, and increased acute response to strong inflammatory stimuli. Transcriptomic and proteomic analyses in acutely isolated adult mouse microglia as well as in human monocyte-derived microglial cells showed that PLC{gamma}2-P522R upregulates mitochondrial fatty acid oxidation and downregulates inflammatory/interferon signaling pathways. Accordingly, PLC{gamma}2-P522R increased mitochondrial respiration in iPSC-derived microglial cells. ConclusionsTogether, these findings suggest that PLC{gamma}2-P522R variant exerts protection against AD-associated {beta}-amyloid and neuronal pathologies via enhancing microglial barrier formation around {beta}-amyloid plaques and suppressing pro-inflammatory activation. Observed changes in fatty acid metabolism and mitochondrial flexibility as well as the downregulation of genes involved in inflammatory signaling pathways suggest that these protective effects of the PLC{gamma}2-P522R variant are mediated through an anti-ageing mechanism.

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Takalo, M., Jeskanen, H., Rolova, T., Kervinen, I., Hellen, M., Heikkinen, S., Koivisto, H., Jokivarsi, K., Muller, S. A., Koivumaki, E.-M., Makinen, P., Juopperi, S.-P., Willman, R.-M., Sinisalo, R., Hoffman, D., Jantti, H., Peitz, M., Fliessbach, K., Kuulasmaa, T., Natunen, T., Kemppainen, S., Poutiainen, P., Leinonen, V., Malm, T., Martiskainen, H., Ramirez, A., Haapasalo, A., Lichtenthaler, S. F., Tanila, H., Haass, C., Rinne, J., Koistinaho, J., Hiltunen, M.. 2024-09-14. Protective variant in PLCgamma2 mitigates Alzheimer's disease associated pathology via enhancing beneficial microglia functions. https://doi.org/10.1101/2024.09.12.612207

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