血小板对流感疫苗的反应反映了衰老的影响

IF 8 1区 医学 Q1 CELL BIOLOGY Aging Cell Pub Date : 2023-01-19 DOI:10.1111/acel.13749
Anna Konstorum, Subhasis Mohanty, Yujiao Zhao, Anthony Melillo, Brent Vander Wyk, Allison Nelson, Sui Tsang, Tamara P. Blevins, Robert?B. Belshe, Daniel G. Chawla, Matthew T. Rondina, Thomas M. Gill, Ruth R. Montgomery, Heather G. Allore, Steven H. Kleinstein, Albert C. Shaw
{"title":"血小板对流感疫苗的反应反映了衰老的影响","authors":"Anna Konstorum,&nbsp;Subhasis Mohanty,&nbsp;Yujiao Zhao,&nbsp;Anthony Melillo,&nbsp;Brent Vander Wyk,&nbsp;Allison Nelson,&nbsp;Sui Tsang,&nbsp;Tamara P. Blevins,&nbsp;Robert?B. Belshe,&nbsp;Daniel G. Chawla,&nbsp;Matthew T. Rondina,&nbsp;Thomas M. Gill,&nbsp;Ruth R. Montgomery,&nbsp;Heather G. Allore,&nbsp;Steven H. Kleinstein,&nbsp;Albert C. Shaw","doi":"10.1111/acel.13749","DOIUrl":null,"url":null,"abstract":"<p>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.</p>","PeriodicalId":119,"journal":{"name":"Aging Cell","volume":"22 2","pages":""},"PeriodicalIF":8.0000,"publicationDate":"2023-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/acel.13749","citationCount":"0","resultStr":"{\"title\":\"Platelet response to influenza vaccination reflects effects of aging\",\"authors\":\"Anna Konstorum,&nbsp;Subhasis Mohanty,&nbsp;Yujiao Zhao,&nbsp;Anthony Melillo,&nbsp;Brent Vander Wyk,&nbsp;Allison Nelson,&nbsp;Sui Tsang,&nbsp;Tamara P. Blevins,&nbsp;Robert?B. Belshe,&nbsp;Daniel G. Chawla,&nbsp;Matthew T. Rondina,&nbsp;Thomas M. Gill,&nbsp;Ruth R. Montgomery,&nbsp;Heather G. Allore,&nbsp;Steven H. Kleinstein,&nbsp;Albert C. Shaw\",\"doi\":\"10.1111/acel.13749\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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.</p>\",\"PeriodicalId\":119,\"journal\":{\"name\":\"Aging Cell\",\"volume\":\"22 2\",\"pages\":\"\"},\"PeriodicalIF\":8.0000,\"publicationDate\":\"2023-01-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/acel.13749\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Aging Cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/acel.13749\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aging Cell","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/acel.13749","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

血小板不仅是止血的介质,也是先天免疫的介质。然而,在免疫应答过程中,年龄和老年性疾病(如虚弱)如何影响血小板功能仍不清楚。我们评估了年轻(21-35岁)和老年(≥65岁)成年人(包括大部分非虚弱的社区居民和熟练护理机构(SNF)居住的成年人,他们几乎都符合虚弱的标准)在基线和接种流感疫苗后的血小板转录组。在接种疫苗之前,我们观察到血小板活化和线粒体rna表达的年龄相关增加,编码介导翻译的蛋白质的rna表达减少。接种疫苗后28天的反应轨迹也发现了年龄相关差异。通过张量分解分析,我们发现在年轻参与者中血小板激活途径基因的RNA表达增加,但在(SNF)居住的成年人中水平下降。翻译RNA轨迹与这些激活途径呈负相关。与接种前后的年轻人相比,在蛋白质水平上,居住在社区的老年人的血小板活化都有所增强;而与社区居住的老年人相比,SNF居民的血小板活化程度降低,这可能反映了翻译RNA表达降低的影响。我们的研究结果揭示了血小板转录组和激活反应的改变可能导致老年人年龄相关的慢性炎症以及血栓性和促炎性疾病的发病率增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Platelet response to influenza vaccination reflects effects of aging

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
期刊最新文献
Residual microglia following short-term PLX5622 treatment in 5xFAD mice exhibit diminished NLRP3 inflammasome and mTOR signaling, and enhanced autophagy. Isolating the direct effects of growth hormone on lifespan and metabolism in mice. The soil Mycobacterium sp. promotes health and longevity through different bacteria-derived molecules in Caenorhabditis elegans. Correction to "Higher expression of denervation-responsive genes is negatively associated with muscle volume and performance traits in the study of muscle, mobility, and aging (SOMMA)". A small-molecule screen identifies novel aging modulators by targeting 5-HT/DA signaling pathway.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1