Lifespan extension with preservation of hippocampal function in aged system x-deficient male mice.

Verbruggen, Lise;Ates, Gamze;Lara, Olaya;De Munck, Jolien;Massie, Ann;et.al.
(2022) Molecular Psychiatry — Vol. 27, n° 4, p. 2355-2368 (2022)

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Authors
  • Verbruggen, Lise
    Author
  • Ates, Gamzeorcid-logo
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  • Lara, Olayaorcid-logo
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  • De Munck, Jolienorcid-logo
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  • Beckers, Paulineorcid-logoUCLouvain
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  • Massie, Annorcid-logo
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Abstract
The cystine/glutamate antiporter system x has been identified as the major source of extracellular glutamate in several brain regions as well as a modulator of neuroinflammation, and genetic deletion of its specific subunit xCT (xCT) is protective in mouse models for age-related neurological disorders. However, the previously observed oxidative shift in the plasma cystine/cysteine ratio of adult xCT mice led to the hypothesis that system x deletion would negatively affect life- and healthspan. Still, till now the role of system x in physiological aging remains unexplored. We therefore studied the effect of xCT deletion on the aging process of mice, with a particular focus on the immune system, hippocampal function, and cognitive aging. We observed that male xCT mice have an extended lifespan, despite an even more increased plasma cystine/cysteine ratio in aged compared to adult mice. This oxidative shift does not negatively impact the general health status of the mice. On the contrary, the age-related priming of the innate immune system, that manifested as increased LPS-induced cytokine levels and hypothermia in xCT mice, was attenuated in xCT mice. While this was associated with only a very moderate shift towards a more anti-inflammatory state of the aged hippocampus, we observed changes in the hippocampal metabolome that were associated with a preserved hippocampal function and the retention of hippocampus-dependent memory in male aged xCT mice. Targeting system x is thus not only a promising strategy to prevent cognitive decline, but also to promote healthy aging.
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Citations

Verbruggen, L., Ates, G., Lara, O., De Munck, J., Villers, A., De Pauw, L., Ottestad-Hansen, S., Kobayashi, S., Beckers, P., Janssen, P., Sato, H., Zhou, Y., Hermans, E., Njemini, R., Arckens, L., Danbolt, N. C., De Bundel, D., Aerts, J. L., Barbé, K., et al. (2022). Lifespan extension with preservation of hippocampal function in aged system x-deficient male mice. Molecular Psychiatry, 27(4), 2355-2368. https://doi.org/10.1038/s41380-022-01470-5 (Original work published 2022)