青少年非酒精性脂肪性肝病患者生活方式干预后循环细胞外囊泡蛋白质组货物的变化。

Changes in proteomic cargo of circulating extracellular vesicles in response to lifestyle intervention in adolescents with hepatic steatosis.

机构信息

Diabetes and Metabolic Disease Research Unit, Translational Genomics Research Institute, Phoenix, AZ, USA.

Neurogenomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.

出版信息

Clin Nutr ESPEN. 2024 Apr;60:333-342. doi: 10.1016/j.clnesp.2024.02.024. Epub 2024 Feb 23.

Abstract

BACKGROUND

Recent studies suggest that proteomic cargo of extracellular vesicles (EVs) may play a role in metabolic improvements following lifestyle interventions. However, the relationship between changes in liver fat and circulating EV-derived protein cargo following intervention remains unexplored.

METHODS

The study cohort comprised 18 Latino adolescents with obesity and hepatic steatosis (12 males/6 females; average age 13.3 ± 1.2 y) who underwent a six-month lifestyle intervention. EV size distribution and concentration were determined by light scattering intensity; EV protein composition was characterized by liquid chromatography tandem-mass spectrometry.

RESULTS

Average hepatic fat fraction (HFF) decreased 23% by the end of the intervention (12.5% [5.5] to 9.6% [4.9]; P = 0.0077). Mean EV size was smaller post-intervention compared to baseline (120.2 ± 16.4 nm to 128.4 ± 16.5 nm; P = 0.031), although the difference in mean EV concentration (1.1E+09 ± 4.1E+08 particles/mL to 1.1E+09 ± 1.8E+08 particles/mL; P = 0.656)) remained unchanged. A total of 462 proteins were identified by proteomic analysis of plasma-derived EVs from participants pre- and post-intervention, with 113 proteins showing differential abundance (56 higher and 57 lower) between the two timepoints (adj-p <0.05). Pathway analysis revealed enrichment in complement cascade, initial triggering of complement, creation of C4 and C2 activators, and regulation of complement cascade. Hepatocyte-specific EV affinity purification identified 40 proteins with suggestive (p < 0.05) differential abundance between pre- and post-intervention samples.

CONCLUSIONS

Circulating EV-derived proteins, particularly those associated with the complement cascade, may contribute to improvements in liver fat in response to lifestyle intervention.

摘要

背景

最近的研究表明,细胞外囊泡(EVs)的蛋白质组货物可能在生活方式干预后代谢改善中发挥作用。然而,干预后肝脂肪和循环 EV 衍生蛋白货物变化之间的关系尚未探索。

方法

研究队列包括 18 名拉丁裔肥胖和肝脂肪变性的青少年(12 名男性/6 名女性;平均年龄 13.3±1.2 岁),他们接受了为期六个月的生活方式干预。通过光散射强度确定 EV 大小分布和浓度;通过液相色谱串联质谱法描述 EV 蛋白组成。

结果

干预结束时,平均肝脂肪分数(HFF)下降了 23%(12.5%[5.5]至 9.6%[4.9];P=0.0077)。与基线相比,干预后平均 EV 大小较小(120.2±16.4nm 至 128.4±16.5nm;P=0.031),尽管平均 EV 浓度(1.1E+09±4.1E+08 个颗粒/mL 至 1.1E+09±1.8E+08 个颗粒/mL;P=0.656)无变化。通过对干预前后参与者的血浆衍生 EV 进行蛋白质组分析,共鉴定出 462 种蛋白质,其中 113 种蛋白质在两个时间点之间表现出差异丰度(56 种上调和 57 种下调)(adj-p<0.05)。途径分析显示补体级联、补体初始触发、C4 和 C2 激活物的产生以及补体级联的调节富集。肝细胞特异性 EV 亲和纯化鉴定出 40 种具有提示意义(p<0.05)的蛋白在干预前后样本中差异丰度。

结论

循环 EV 衍生蛋白,特别是与补体级联相关的蛋白,可能有助于生活方式干预后肝脂肪的改善。

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