Department of Pathology, Yale School of Medicine, New Haven, Connecticut, USA.
Department of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, Connecticut, USA.
Aging Cell. 2023 Feb;22(2):e13749. doi: 10.1111/acel.13749. Epub 2023 Jan 19.
Platelets are uniquely positioned as mediators of not only hemostasis but also innate immunity. However, how age and geriatric conditions such as frailty influence platelet function during an immune response remains unclear. We assessed the platelet transcriptome at baseline and following influenza vaccination in Younger (age 21-35) and Older (age ≥65) adults (including community-dwelling individuals who were largely non-frail and skilled nursing facility (SNF)-resident adults who nearly all met criteria for frailty). Prior to vaccination, we observed an age-associated increase in the expression of platelet activation and mitochondrial RNAs and decrease in RNAs encoding proteins mediating translation. Age-associated differences were also identified in post-vaccination response trajectories over 28 days. Using tensor decomposition analysis, we found increasing RNA expression of genes in platelet activation pathways in young participants, but decreasing levels in (SNF)-resident adults. Translation RNA trajectories were inversely correlated with these activation pathways. Enhanced platelet activation was found in community-dwelling older adults at the protein level, compared to young individuals both prior to and post-vaccination; whereas SNF residents showed decreased platelet activation compared to community-dwelling older adults that could reflect the influence of decreased translation RNA expression. Our results reveal alterations in the platelet transcriptome and activation responses that may contribute to age-associated chronic inflammation and the increased incidence of thrombotic and pro-inflammatory diseases in older adults.
血小板作为止血和先天免疫的介质具有独特的地位。然而,年龄和衰弱等老年疾病如何影响免疫反应期间的血小板功能仍不清楚。我们评估了年轻(年龄 21-35 岁)和老年(年龄≥65 岁)成年人(包括主要非衰弱的社区居住者和几乎都符合衰弱标准的熟练护理设施(SNF)居民)在基线和流感疫苗接种后的血小板转录组。在接种疫苗之前,我们观察到血小板活化和线粒体 RNA 的表达随年龄增加,而编码翻译中介蛋白的 RNA 减少。在 28 天的疫苗接种后反应轨迹中也发现了与年龄相关的差异。使用张量分解分析,我们发现年轻参与者中血小板活化途径的基因 RNA 表达增加,但 SNF 居民中的水平降低。翻译 RNA 轨迹与这些活化途径呈负相关。与年轻个体相比,接种疫苗前后,社区居住的老年成年人在蛋白质水平上表现出增强的血小板活化;而 SNF 居民的血小板活化减少,这可能反映出翻译 RNA 表达减少的影响。我们的研究结果揭示了血小板转录组和激活反应的改变,这些改变可能导致与年龄相关的慢性炎症以及老年成年人中血栓形成和促炎疾病的发生率增加。