Elucidating the pathogenic mechanisms of AD brain-derived tau-containing extracellular vesicles: Highly transmissible and preferential propagation to GABAergic neurons

Ruan, Z.; Pathak, D.; Kalavai, S. V.; Yoshii-Kitahara, A.; Muraoka, S.; Takamatsu-Yukawa, K.; Hu, J.; Wang, Y.; Hersh, S.; Gorantla, S.; Kayed, R.; Gendelman, H.; Ikezu, S.; Luebke, J. I.; Ikezu, T.

doi:10.1101/2020.03.15.992719

bioRxiv · 10.1101/2020.03.15.992719

Elucidating the pathogenic mechanisms of AD brain-derived tau-containing extracellular vesicles: Highly transmissible and preferential propagation to GABAergic neurons

Ruan, Z.·Pathak, D.·Kalavai, S. V.·Yoshii-Kitahara, A.·Muraoka, S.·Takamatsu-Yukawa, K.·Hu, J.·Wang, Y.·Hersh, S.·Gorantla, S.·Kayed, R.·Gendelman, H.·Ikezu, S.·Luebke, J. I.·Ikezu, T.

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Abstract

Extracellular vesicles (EVs) propagate tau pathology for Alzheimers disease (AD). How EV transmission influences AD are, nonetheless, poorly understood. To these ends, the physicochemical and molecular structure-function relationships of human brain-derived EVs, from AD and prodromal AD (pAD), were compared to non-demented controls (CTRL). AD EVs were shown to be significantly enriched in epitope-specific tau oligomers versus pAD or CTRL EVs assayed by dot-blot and atomic force microscopy tests. AD EVs were efficiently internalized by murine cortical neurons and transferred tau with higher aggregation potency than pAD and CTRL EVs. Strikingly, inoculation of tau-containing AD EVs into the outer molecular layer of the dentate gyrus induced tau propagation throughout the hippocampus. This was seen in 22 months-old C57BL/6 mice at 4.5 months post-injection by semiquantitative brain-wide immunohistochemistry tests with multiple anti-phospho-tau (p-tau) antibodies. Inoculation of the equal amount of tau from CTRL EVs or as oligomer or fibril-enriched fraction from the same AD donor showed little propagation. AD EVs induced tau accumulation in the hippocampus as oligomers or sarkosyl-insoluble proteins. Unexpectedly, p-tau cells were mostly GAD67+ GABAergic neurons and to a lesser extent, GluR2/3+ excitatory mossy cells, showing preferential EV-mediated GABAergic neuronal tau propagation. Whole-cell patch clamp recording of Cornu Ammonis (CA1) pyramidal cells showed significant reduction in the amplitude of spontaneous inhibitory post-synaptic currents. This was accompanied by reductions in c-fos+ GAD67+GABAergic neurons and GAD67+ GABAergic neuronal puncta surrounding pyramidal neurons in the CA1 region confirming reduced interneuronal projections. Our study posits a novel tau-associated pathological mechanism for brain-derived EVs.

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Ruan, Z., Pathak, D., Kalavai, S. V., Yoshii-Kitahara, A., Muraoka, S., Takamatsu-Yukawa, K., Hu, J., Wang, Y., Hersh, S., Gorantla, S., Kayed, R., Gendelman, H., Ikezu, S., Luebke, J. I., Ikezu, T.. 2020-03-15. Elucidating the pathogenic mechanisms of AD brain-derived tau-containing extracellular vesicles: Highly transmissible and preferential propagation to GABAergic neurons. https://doi.org/10.1101/2020.03.15.992719

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