Institute for Genetic and Biomedical Research, National Research Council (CNR), 08045 Lanusei, Italy.
Laboratory of Genetics and Genomics, National Institute on Ageing, National Institutes of Health, Baltimore, MD 21224, USA.
Int J Mol Sci. 2023 Apr 13;24(8):7183. doi: 10.3390/ijms24087183.
Extracellular vesicles (EVs) mediate cell interactions in biological processes, such as receptor activation or molecule transfer. Estimates of variation by age and sex have been limited by small sample size, and no report has assessed the contribution of genetic factors to levels of EVs. Here, we evaluated blood levels of 25 EV and 3 platelet traits in 974 individuals (933 genotyped) and reported the first genome-wide association study (GWAS) on levels of these traits. EV levels all decreased with age, whereas the trend for their surface markers was more heterogeneous. Platelets and CD31dim platelet EVs significantly increased in females compared to males, although CD31 expression on both platelets and platelet EVs decreased in females. Levels of the other EV subsets were similar between sexes. GWAS revealed three statistically significant genetic signals associated with EV levels in the and genes and in the intergenic region between and . These add to a signal in the 3'UTR of associated with CD31 expression on platelets that was previously found to be associated with other platelet traits. These findings suggest that EV formation is not a simple, constant adjunct of metabolism but is under both age-related and genetic control that can be independent of the regulation of the levels of the cells from which the EVs derive.
细胞外囊泡 (EVs) 在生物过程中介导细胞相互作用,如受体激活或分子转移。由于样本量小,对年龄和性别变化的估计受到限制,并且没有报告评估遗传因素对 EV 水平的贡献。在这里,我们评估了 974 个人(933 个基因分型)的 25 种 EV 和 3 种血小板特征的血液水平,并报告了这些特征水平的第一项全基因组关联研究 (GWAS)。EV 水平随年龄的增长而降低,而其表面标志物的趋势更为复杂。与男性相比,女性的血小板和 CD31dim 血小板 EV 显著增加,尽管女性的血小板和血小板 EV 上的 CD31 表达均减少。其他 EV 亚群在性别之间的水平相似。GWAS 显示与 和 基因中的 EV 水平以及 和 之间的基因间区域相关的三个具有统计学意义的遗传信号。这些信号增加了先前与其他血小板特征相关的与血小板上 CD31 表达相关的 3'UTR 中的信号。这些发现表明,EV 的形成不是代谢的简单、恒定的附属物,而是受到年龄相关和遗传控制的影响,并且可以独立于 EV 来源细胞水平的调节。