Young Plasma Rejuvenates Blood Dna Methylation Profile, Extends Mean Lifespan And Improves Physical Appearance In Old Rats

Priscila Chiavellini, Marianne Lehmann, Maria D Gallardo, Martina Canatelli Mallat, Diana C Pasquini, Joseph A Zoller, Juozas Gordevicius, Mauricio Girard, Ezequiel Lacunza, Claudia B Herenu, Steve Horvath, Rodolfo G Goya
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Abstract

There is converging evidence that young blood conveys cells, vesicles and molecules able to revitalize function and restore organ integrity in old individuals. We assessed the effects of young plasma on the lifespan, epigenetic age and healthspan of old female rats. Beginning at 25.6 months of age, a group of 9 rats (group T) was i.p. injected with plasma from young rats until their natural death. A group of 8 control rats of the same age received no treatment (group C). Blood samples were collected every other week. Survival curves showed that from age 26 to 30 months, none of the group T animals died, whereas the survival curve of group C rats began to decline at age 26 months. Blood DNAm age versus chronological age showed that DNAm age in young animals increased faster than chronological age, then slowed down, entering a plateau after 27 months. The DNAm age of the treated rats fell below the DNAm age of controls and, in numerical terms, remained consistently lower until natural death. When rats were grouped according to the similarities in their differential blood DNA methylation profile, samples from the treated and control rats clustered in separate groups. Analysis of promoter differential methylation in genes involved in systemic regulatory activities revealed specific GO term enrichment related to the insulin-like factors pathways as well as to cytokines and chemokines associated with immune and homeostatic functions. We conclude that young plasma therapy may constitute a natural noninvasive intervention for epigenetic rejuvenation and health enhancement.
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年轻血浆可使血液 DNA 甲基化轮廓年轻化,延长老龄大鼠的平均寿命并改善其体貌特征
有越来越多的证据表明,年轻血液中输送的细胞、囊泡和分子能够振兴老年人的功能并恢复器官的完整性。我们评估了年轻血浆对老年雌性大鼠寿命、表观遗传年龄和健康寿命的影响。从 25.6 个月大的大鼠开始,给一组 9 只大鼠(T 组)注射年轻大鼠的血浆,直到它们自然死亡。8 只同龄对照组大鼠未接受任何治疗(C 组)。每隔一周采集一次血液样本。生存曲线显示,从 26 个月大到 30 个月大,T 组大鼠无一死亡,而 C 组大鼠的生存曲线在 26 个月大时开始下降。血液中DNAm年龄与实际年龄的对比显示,幼鼠DNAm年龄的增长速度快于实际年龄的增长速度,然后放缓,在27个月后进入平稳期。接受治疗的大鼠的DNAm年龄低于对照组的DNAm年龄,而且从数值上看,一直持续较低,直到自然死亡。当根据大鼠血液 DNA 甲基化差异图谱的相似性对大鼠进行分组时,治疗大鼠和对照组大鼠的样本被分成了不同的组。对参与系统调节活动的基因启动子差异甲基化的分析表明,特定的 GO 术语富集与胰岛素样因子通路以及与免疫和平衡功能相关的细胞因子和趋化因子有关。我们得出的结论是,年轻血浆疗法可能是一种天然的非侵入性干预措施,可用于表观遗传年轻化和增强健康。
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