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bioRxiv · 10.1101/2024.01.20.576443

IMPDH2 filaments protect from neurodegeneration in AMPD2 deficiency

Flores-Mendez, M.·Ohl, L.·Roule, T.·Zhou, Y.·Tintos-Hernandez, J. A.·Walsh, K.·Ortiz-Gonzalez, X. R.·Akizu, N.
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Abstract

Metabolic dysregulation is one of the most common causes of pediatric neurodegenerative disorders. However, how the disruption of ubiquitous and essential metabolic pathways predominantly affect neural tissue remains unclear. Here we use mouse models of AMPD2 deficiency to study cellular and molecular mechanisms that lead to selective neuronal vulnerability to purine metabolism imbalance. We show that AMPD deficiency in mice primarily leads to hippocampal dentate gyrus degeneration despite causing a generalized reduction of brain GTP levels. Remarkably, we found that neurodegeneration resistant regions accumulate micron sized filaments of IMPDH2, the rate limiting enzyme in GTP synthesis. In contrast, IMPDH2 filaments are barely detectable in the hippocampal dentate gyrus, which shows a progressive neuroinflammation and neurodegeneration. Furthermore, using a human AMPD2 deficient neural cell culture model, we show that blocking IMPDH2 polymerization with a dominant negative IMPDH2 variant, impairs AMPD2 deficient neural progenitor growth. Together, our findings suggest that IMPDH2 polymerization prevents detrimental GTP deprivation in neurons with available GTP precursor molecules, providing resistance to neurodegeneration. Our findings open the possibility of exploring the involvement of IMPDH2 assembly as a therapeutic intervention for neurodegeneration.

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Flores-Mendez, M., Ohl, L., Roule, T., Zhou, Y., Tintos-Hernandez, J. A., Walsh, K., Ortiz-Gonzalez, X. R., Akizu, N.. 2024-01-22. IMPDH2 filaments protect from neurodegeneration in AMPD2 deficiency. https://doi.org/10.1101/2024.01.20.576443

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