4.4 Article

Platelet factors are induced by longevity factor klotho and enhance cognition in young and aging mice

Journal

NATURE AGING
Volume -, Issue -, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s43587-023-00468-0

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Platelet factors regulate wound healing and can signal from the blood to the brain. This study shows that the platelet factor 4 (PF4) can permeate the brain and enhance cognition. Systemic administration of klotho, a protein that enhances longevity and cognition, increases the levels of platelet factors, including PF4, in mice. PF4 treatment improves synaptic plasticity and cognition in young mice, and decreases cognitive deficits and restores aging-induced changes in hippocampal factors in old mice.
Platelet factors regulate wound healing and can signal from the blood to the brain(1,2). However, whether platelet factors modulate cognition, a highly valued and central manifestation of brain function, is unknown. Here we show that systemic platelet factor 4 (PF4) permeates the brain and enhances cognition. We found that, in mice, peripheral administration of klotho, a longevity and cognition-enhancing protein(3-7), increased the levels of multiple platelet factors in plasma, including PF4. A pharmacologic intervention that inhibits platelet activation blocked klotho-mediated cognitive enhancement, indicating that klotho may require platelets to enhance cognition. To directly test the effects of platelet factors on the brain, we treated mice with vehicle or systemic PF4. In young mice, PF4 enhanced synaptic plasticity and cognition. In old mice, PF4 decreased cognitive deficits and restored aging-induced increases of select factors associated with cognitive performance in the hippocampus. The effects of klotho on cognition were still present in mice lacking PF4, suggesting this platelet factor is sufficient to enhance cognition but not necessary for the effects of klotho-and that other unidentified factors probably contribute. Augmenting platelet factors, possible messengers of klotho, may enhance cognition in the young brain and decrease cognitive deficits in the aging brain.

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