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Nlrp3 基因在循环白细胞中的表达在健康衰老过程中下降。

Nlrp3 Gene Expression in Circulating Leukocytes Declines During Healthy Aging.

机构信息

Univ. Bourgogne Franche-Comté, Biologie Animale Cellulaire et Moléculaire, INSERM U866, Dijon, France.

Univ. Bourgogne Franche-Comté, INSERM U1231 "Lipides, Nutrition, Cancer", CADIR, Dijon, France.

出版信息

J Gerontol A Biol Sci Med Sci. 2018 Jul 9;73(8):1045-1049. doi: 10.1093/gerona/gly018.

Abstract

Aging is often associated with elevated levels of low grade inflammation supposed to drive age-associated diseases. Here, we conducted a cross-sectional study on 58 healthy volunteers, aged from 19 to 81, to investigate the relationship between age and the expression of three inflammasome component genes (Nlrp3, Asc, Casp1), the up-stream transcription factor NFkB, and the pro-inflammatory cytokine Il-1β in leukocytes. We also assessed C-reactive protein (CRP) and IL-1β in plasma, as additional inflammatory markers. We did not find any support to the hypothesis that inflammasone activation increases with age. Expression of Asc, Casp1, NFkB, and Il-1β did not vary with age, body mass index (BMI), and CRP levels. In addition, expression did not differ between males and females or between smokers and non-smokers. A notable exception was the expression of Nlrp3 which varied non-linearly with age. Specifically, Nlrp3 expression strongly declined during aging, in subjects who were between 50 and 81 years old. CRP was higher in women and increased as a function of age-corrected BMI, while only four subjects showed detectable amount of IL-1β in plasma. Further work on larger cohorts with a longitudinal monitoring should be conducted to corroborate the finding that healthy aging is associated with a decrease in inflammasome activation.

摘要

衰老是与低度炎症水平升高相关的,这种低度炎症被认为是导致与年龄相关疾病的原因。在这里,我们对 58 名年龄在 19 至 81 岁之间的健康志愿者进行了横断面研究,以调查年龄与三种炎症小体成分基因(Nlrp3、Asc、Casp1)、上游转录因子 NFkB 和白细胞介素-1β(IL-1β)表达之间的关系。我们还评估了血浆中的 C 反应蛋白(CRP)和 IL-1β,作为额外的炎症标志物。我们没有发现任何证据支持炎症小体激活随年龄增长而增加的假说。Asc、Casp1、NFkB 和 IL-1β的表达与年龄、体重指数(BMI)和 CRP 水平无关。此外,表达在男性和女性之间或吸烟者和非吸烟者之间没有差异。一个值得注意的例外是 Nlrp3 的表达,它与年龄呈非线性变化。具体来说,Nlrp3 的表达在 50 至 81 岁的受试者中随衰老而强烈下降。CRP 在女性中较高,并随年龄校正 BMI 的增加而增加,而只有 4 名受试者的血浆中检测到可检测量的 IL-1β。应该对更大的队列进行纵向监测,以进一步证实健康衰老与炎症小体激活的降低有关的发现。

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