Nature · 2023 · 251 citations · 52 references
Life SciencesImmunologyNeuroscienceAgingInflammationNeuroimmunologyAge-related Physiological ChangesBiological AgingCognitive AgingCognitive ImpairmentNeuroinflammationNeuroprotectionAge-related Immune DeclineAge-related NeuroinflammationAging-related Immune DysfunctionAging-related InflammationHippocampal AgingHippocampal InflammationSynaptic Plasticity ModulationSystemic Administration
. Here we show that platelet factors transfer the benefits of young blood to the ageing brain. Systemic exposure of aged male mice to a fraction of blood plasma from young mice containing platelets decreased neuroinflammation in the hippocampus at the transcriptional and cellular level and ameliorated hippocampal-dependent cognitive impairments. Circulating levels of the platelet-derived chemokine platelet factor 4 (PF4) (also known as CXCL4) were elevated in blood plasma preparations of young mice and humans relative to older individuals. Systemic administration of exogenous PF4 attenuated age-related hippocampal neuroinflammation, elicited synaptic-plasticity-related molecular changes and improved cognition in aged mice. We implicate decreased levels of circulating pro-ageing immune factors and restoration of the ageing peripheral immune system in the beneficial effects of systemic PF4 on the aged brain. Mechanistically, we identified CXCR3 as a chemokine receptor that, in part, mediates the cellular, molecular and cognitive benefits of systemic PF4 on the aged brain. Together, our data identify platelet-derived factors as potential therapeutic targets to abate inflammation and rescue cognition in old age.
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Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
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STAR: ultrafast universal RNA-seq aligner
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