A complex human gut microbiome cultured in an anaerobic intestine-on-a-chip (vol 3, pg 583, 2019)

被引:25
作者
Jalili-Firoozinezhad, Sasan
Gazzaniga, Francesca S.
Calamari, Elizabeth L.
Camacho, Diogo M.
Fadel, Cicely W.
Bein, Amir
Swenor, Ben
Nestor, Bret
Cronce, Michael J.
Tovaglieri, Alessio
Levy, Oren
Gregory, Katherine E.
Breault, David T.
Cabral, Joaquim M. S.
Kasper, Dennis L.
Novak, Richard
Ingber, Donald E.
机构
[1] Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA
[2] Department of Bioengineering and Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Lisbon
[3] Department of Immunology, Harvard Medical School, Boston, MA
[4] Department of Health Sciences and Technology, ETH Zurich, Zurich
[5] Department of Pediatric Newborn Medicine, Brigham and Women’s Hospital, Boston, MA
[6] Department of Pediatrics, Harvard Medical School, Boston, MA
[7] Department of Endocrinology, Boston Children’s Hospital, Boston, MA
[8] Harvard Stem Cell Institute, Cambridge, MA
[9] Vascular Biology Program and Department of Surgery, Boston Children’s Hospital and Harvard Medical School, Boston, MA
[10] Harvard John A. Paulson School of Engineering and Applied Sciences, Cambridge, MA
关键词
D O I
10.1038/s41551-019-0428-x
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The diverse bacterial populations that comprise the commensal microbiome of the human intestine play a central role in health and disease. A method that sustains complex microbial communities in direct contact with living human intestinal cells and their overlying mucus layer in vitro would thus enable the investigation of host–microbiome interactions. Here, we show the extended coculture of living human intestinal epithelium with stable communities of aerobic and anaerobic human gut microbiota, using a microfluidic intestine-on-a-chip that permits the control and real-time assessment of physiologically relevant oxygen gradients. When compared to aerobic coculture conditions, the establishment of a transluminal hypoxia gradient in the chip increased intestinal barrier function and sustained a physiologically relevant level of microbial diversity, consisting of over 200 unique operational taxonomic units from 11 different genera and an abundance of obligate anaerobic bacteria, with ratios of Firmicutes and Bacteroidetes similar to those observed in human faeces. The intestine-on-a-chip may serve as a discovery tool for the development of microbiome-related therapeutics, probiotics and nutraceuticals. © 2019, The Author(s), under exclusive licence to Springer Nature Limited.
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页码:583 / 583
页数:1
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