生物
益生菌
肠道菌群
小肠
免疫系统
动物
细胞生物学
生态学
微生物学
免疫学
细菌
生物化学
遗传学
作者
Benjamin A. H. Jensen,Marc Heyndrickx,Daisy Jonkers,Alan R. Mackie,Sam Millet,Malwina Naghibi,Simone Isling Pærregaard,Bruno Pot,Delphine Saulnier,Christian Sina,Luc Sterkman,Pieter Van den Abbeele,Naomi Venlet,Erwin G. Zoetendal,Arthur Constantijn Ouwehand
标识
DOI:10.1016/j.xcrm.2023.101190
摘要
Research on gut microbiota has generally focused on fecal samples, representing luminal content of the large intestine. However, nutrient uptake is restricted to the small intestine. Abundant immune cell populations at this anatomical site combined with diminished mucus secretion and looser junctions (partly to allow for more efficient fluid and nutrient absorption) also results in intimate host-microbe interactions despite more rapid transit. It is thus crucial to dissect key differences in both ecology and physiology between small and large intestine to better leverage the immense potential of human gut microbiota imprinting, including probiotic engraftment at biological sensible niches. Here, we provide a detailed review unfolding how the physiological and anatomical differences between the small and large intestine affect gut microbiota composition, function, and plasticity. This information is key to understanding how gut microbiota manipulation, including probiotic administration, may strain-dependently transform host-microbe interactions at defined locations.
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