Department of Infection, Immunity and Cardiovascular Disease, Medical School, University of Sheffield, Sheffield, United Kingdom.
Healthy Lifespan Institute, University of Sheffield, Sheffield, United Kingdom.
Front Immunol. 2023 Jul 13;14:1222308. doi: 10.3389/fimmu.2023.1222308. eCollection 2023.
Ageing research is establishing macrophages as key immune system regulators that undergo functional decline. Due to heterogeneity between species and tissue populations, a plethora of data exist and the power of scientific conclusions can vary substantially. This meta-analysis by information content (MAIC) and systematic literature review (SLR) aims to determine overall changes in macrophage gene and protein expression, as well as function, with age.
PubMed was utilized to collate peer-reviewed literature relating to macrophage ageing. Primary studies comparing macrophages in at least two age groups were included. Data pertaining to gene or protein expression alongside method used were extracted for MAIC analysis. For SLR analysis, data included all macrophage-specific changes with age, as well as species, ontogeny and age of groups assessed.
A total of 240 studies were included; 122 of which qualified for MAIC. The majority of papers focussed on changes in macrophage count/infiltration as a function of age, followed by gene and protein expression. The MAIC found iNOS and TNF to be the most commonly investigated entities, with 328 genes and 175 proteins showing consistent dysregulation with age across the literature. Overall findings indicate that cytokine secretion and phagocytosis are reduced and reactive oxygen species production is increased in the ageing macrophage.
Collectively, our analysis identifies critical regulators in macrophage ageing that are consistently dysregulated, highlighting a plethora of targets for further investigation. Consistent functional changes with age found here can be used to confirm an ageing macrophage phenotype in specific studies and experimental models.
衰老研究表明巨噬细胞是关键的免疫系统调节剂,其功能会随着年龄的增长而衰退。由于物种和组织群体之间存在异质性,因此存在大量数据,科学结论的说服力也会有很大差异。本研究通过信息内容(MAIC)和系统文献综述(SLR)旨在确定巨噬细胞基因和蛋白质表达以及功能随年龄变化的总体情况。
使用 PubMed 整理与巨噬细胞衰老相关的同行评议文献。纳入比较至少两个年龄组巨噬细胞的原始研究。提取与 MAIC 分析相关的基因或蛋白质表达以及使用方法的数据。对于 SLR 分析,数据包括与年龄相关的所有巨噬细胞特异性变化,以及评估的物种、个体发生和年龄组。
共纳入 240 项研究,其中 122 项符合 MAIC 标准。大多数论文侧重于巨噬细胞数量/浸润随年龄变化的功能,其次是基因和蛋白质表达。MAIC 发现 iNOS 和 TNF 是最常研究的实体,文献中有 328 个基因和 175 个蛋白质显示与年龄相关的一致失调。总体研究结果表明,衰老巨噬细胞中细胞因子分泌和吞噬作用减少,活性氧产生增加。
我们的分析综合确定了巨噬细胞衰老中一致失调的关键调节因子,突出了大量有待进一步研究的靶点。这里发现的与年龄一致的功能变化可用于在特定研究和实验模型中确认衰老巨噬细胞表型。