Zeber-Lubecka Natalia, Kulecka Maria, Balabas Aneta, Czarnowski Pawel, Pyśniak Kazimiera, Dąbrowska Michalina, Ostrowski Jerzy, Hennig Ewa E
Department of Gastroenterology, Hepatology and Clinical Oncology, Centre of Postgraduate Medical Education, 02-781 Warsaw, Poland.
Department of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, Poland.
Biology (Basel). 2025 Sep 17;14(9):1278. doi: 10.3390/biology14091278.
Apolipoprotein A-IV (ApoA-IV) has been implicated in modulating the gut microbiota. However, chronic high-fat diet (HFD) consumption impairs ApoA-IV signaling and disrupts gut microbial balance, contributing to obesity and insulin resistance. This study aimed to investigate the role of ApoA-IV in shaping the gut microbiota and associated metabolic profiles throughout the lifespan of mice exposed to an HFD. Fecal samples were collected from ApoA-IV knockout (KO) and wild-type mice at five time points for microbiota and metabolite profiling using 16S rRNA gene sequencing and gas chromatography-mass spectrometry, respectively. Lifespan was longest in ApoA-IV-KO mice on a normal diet, while the HFD reduced survival across genotypes. Microbiota analysis revealed diet- and age-dependent shifts, including an elevated Firmicutes/Bacteroidota ratio, altered abundance of and reduced in ApoA-IV-KO mice on the HFD. Metabolic profiling showed a stronger impact of diet than genotype, with early and persistent increases in branched-chain amino acids and reductions in short-chain fatty acids (SCFAs). ApoA-IV deficiency modulated lifespan microbial and metabolic changes and shaped distinct responses to dietary stress. Despite age-related convergence in microbiota structure, genotype-specific differences in metabolite profiles and SCFA-producing bacteria correlations persisted into old age, demonstrating the lasting impact of ApoA-IV on host metabolic adaptation.
载脂蛋白A-IV(ApoA-IV)与调节肠道微生物群有关。然而,长期食用高脂饮食(HFD)会损害ApoA-IV信号传导并破坏肠道微生物平衡,导致肥胖和胰岛素抵抗。本研究旨在调查ApoA-IV在暴露于HFD的小鼠整个生命周期中对塑造肠道微生物群和相关代谢谱的作用。分别在五个时间点从ApoA-IV基因敲除(KO)小鼠和野生型小鼠收集粪便样本,使用16S rRNA基因测序和气相色谱-质谱法进行微生物群和代谢物分析。正常饮食的ApoA-IV-KO小鼠寿命最长,而HFD降低了各基因型小鼠的存活率。微生物群分析揭示了饮食和年龄依赖性变化,包括HFD喂养的ApoA-IV-KO小鼠中厚壁菌门/拟杆菌门比例升高、特定菌属丰度改变以及某菌属减少。代谢物分析表明,饮食对代谢物的影响比基因型更强,支链氨基酸早期持续增加,短链脂肪酸(SCFA)减少。ApoA-IV缺乏调节了寿命、微生物和代谢变化,并塑造了对饮食应激的不同反应。尽管微生物群结构在年龄增长过程中趋同,但代谢物谱和SCFA产生菌相关性的基因型特异性差异持续到老年,表明ApoA-IV对宿主代谢适应具有持久影响。