Genos Glycobiology Laboratory, Zagreb, Croatia.
Department of Twins Research and Genetic Epidemiology, Kings College London, UK.
J Gerontol A Biol Sci Med Sci. 2014 Jul;69(7):779-89. doi: 10.1093/gerona/glt190. Epub 2013 Dec 10.
Fine structural details of glycans attached to the conserved N-glycosylation site significantly not only affect function of individual immunoglobulin G (IgG) molecules but also mediate inflammation at the systemic level. By analyzing IgG glycosylation in 5,117 individuals from four European populations, we have revealed very complex patterns of changes in IgG glycosylation with age. Several IgG glycans (including FA2B, FA2G2, and FA2BG2) changed considerably with age and the combination of these three glycans can explain up to 58% of variance in chronological age, significantly more than other markers of biological age like telomere lengths. The remaining variance in these glycans strongly correlated with physiological parameters associated with biological age. Thus, IgG glycosylation appears to be closely linked with both chronological and biological ages. Considering the important role of IgG glycans in inflammation, and because the observed changes with age promote inflammation, changes in IgG glycosylation also seem to represent a factor contributing to aging.
Glycosylation is the key posttranslational mechanism that regulates function of immunoglobulins, with multiple systemic repercussions to the immune system. Our study of IgG glycosylation in 5,117 individuals from four European populations has revealed very extensive and complex changes in IgG glycosylation with age. The combined index composed of only three glycans explained up to 58% of variance in age, considerably more than other biomarkers of age like telomere lengths. The remaining variance in these glycans strongly correlated with physiological parameters associated with biological age; thus, IgG glycosylation appears to be closely linked with both chronological and biological ages. The ability to measure human biological aging using molecular profiling has practical applications for diverse fields such as disease prevention and treatment, or forensics.
附着在保守 N-糖基化位点上的聚糖的精细结构细节不仅显著影响单个免疫球蛋白 G(IgG)分子的功能,而且还介导全身性炎症。通过分析来自四个欧洲人群的 5117 个人的 IgG 糖基化,我们揭示了 IgG 糖基化随年龄变化的非常复杂的模式。几种 IgG 聚糖(包括 FA2B、FA2G2 和 FA2BG2)随年龄变化相当大,这三种聚糖的组合可以解释高达 58%的年龄差异,明显超过其他生物年龄标志物,如端粒长度。这些聚糖的剩余方差与与生物年龄相关的生理参数强烈相关。因此,IgG 糖基化似乎与年龄和生物年龄密切相关。考虑到 IgG 聚糖在炎症中的重要作用,并且由于观察到的与年龄相关的变化会促进炎症,因此 IgG 糖基化的变化似乎也代表了导致衰老的一个因素。
糖基化是调节免疫球蛋白功能的关键翻译后机制,对免疫系统有多种全身性影响。我们对来自四个欧洲人群的 5117 个人的 IgG 糖基化研究揭示了 IgG 糖基化随年龄变化的非常广泛和复杂的变化。仅由三种聚糖组成的组合指数解释了高达 58%的年龄差异,明显超过其他年龄标志物,如端粒长度。这些聚糖的剩余方差与与生物年龄相关的生理参数强烈相关;因此,IgG 糖基化似乎与年龄和生物年龄密切相关。使用分子谱图测量人类生物衰老的能力在疾病预防和治疗或法医学等各个领域具有实际应用。