Commercial Dairy Cow Milk microRNAs Resist Digestion under Simulated Gastrointestinal Tract Conditions

被引:150
|
作者
Benmoussa, Abderrahim [1 ,2 ]
Lee, Chan Ho C. [1 ,2 ]
Laffont, Benoit [1 ,2 ]
Savard, Patricia [3 ]
Laugier, Jonathan [1 ,2 ]
Boilard, Eric [1 ,2 ]
Gilbert, Caroline [1 ,2 ]
Fliss, Ismail [3 ]
Provost, Patrick [1 ,2 ]
机构
[1] Univ Laval, Dept Microbiol Infect Dis & Immun, Univ Laval Hosp Ctr, Univ Quebec Hosp Ctr,Res Ctr, Quebec City, PQ, Canada
[2] Univ Laval, Fac Med, Quebec City, PQ, Canada
[3] Univ Laval, Inst Nutr & Funct Foods, STELA Dairy Res Ctr, Quebec City, PQ, Canada
来源
JOURNAL OF NUTRITION | 2016年 / 146卷 / 11期
基金
加拿大健康研究院;
关键词
digestion; exosome; extracellular vesicles; microRNA; milk; TIM-1; IN-VITRO DIGESTION; MESSENGER-RNA; EXTRACELLULAR VESICLES; EXOSOMES; QUANTIFICATION; SYSTEM; CELLS; MIRNAS; MODEL; INFLAMMATION;
D O I
10.3945/jn.116.237651
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: MicroRNAs are small, gene-regulatory noncoding RNA species present in large amounts in milk, where they seem to be protected against degradative conditions, presumably because of their association with exosomes. Objective: We monitored the relative stability of commercial dairy cow milk microRNAs during digestion and examined their associations with extracellular vesicles (EVs). Methods: We used a computer-controlled, in vitro, gastrointestinal model TNO intestinal model-1 (TIM-1) and analyzed, by quantitative polymerase chain reaction, the concentration of 2 microRNAs within gastrointestinal tract compartments at different points in time. EVs within TIM-1 digested and nondigested samples were studied by immunoblotting, dynamic light scattering, quantitative polymerase chain reaction, and density measurements. Results: A large quantity of dairy milk Bos taurus microRNA-223 (bta-miR-223) and bta-miR-125b (similar to 10(9)-10(10)) copies/300 mL milk) withstood digestion under simulated gastrointestinal tract conditions, with the stomach causing the most important decrease in microRNA amounts. A large quantity of these 2 microRNAs (similar to 10(8)-10(9) copies/300 mL milk) was detected in the upper small intestine compartments, which supports their potential bioaccessibility. A protocol optimized for the enrichment of dairy milk exosomes yielded a 100,000 x g pellet fraction that was positive for the exosomal markers tumor susceptibility gene-101 (TSG101), apoptosis-linked gene 2-interacting protein X (ALIX), and heat shock protein 70 (HSP70) and containing bta-miR-223 and bta-miR-125b. This approach, based on successive ultracentrifugation steps, also revealed the existence of ALIX(-), HSP70(-/low), and TSG101(-/low) EVs larger than exosomes and 2-6 times more enriched in bta-miR-223 and bta-miR-125b (P < 0.05). Conclusions: Our findings indicate that commercial dairy cow milk contains numerous microRNAs that can resist digestion and are associated mostly with ALIX(-), HSP70(-/low), and TSG101(-/low) EVs. Our results support the existence of interspecies transfer of microRNAs mediated by milk consumption and challenge our current view of exosomes as the sole carriers of milk-derived microRNAs.
引用
收藏
页码:2206 / 2215
页数:10
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