Human Microphysiological Models of Intestinal Tissue and Gut Microbiome

被引:59
作者
Steinway, Steven N. [1 ]
Saleh, Jad [2 ]
Koo, Bon-Kyoung [3 ]
Delacour, Delphine [2 ]
Kim, Deok-Ho [1 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Paris Diderot Univ, Inst Jacques Monod, Cell Adhes & Mech, CNRS UMR 7592, Paris, France
[3] Austrian Acad Sci IMBA, Vienna Bioctr VBC, Inst Mol Biotechnol, Vienna, Austria
[4] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
关键词
microphysiological model; gut-on-a-chip; organ chip; microbiome; intestinal tissue; organoid; microfluidics; IN-VITRO EXPANSION; PLURIPOTENT STEM-CELLS; EXTRACELLULAR-MATRIX; MOUSE SMALL; ORGANOIDS; CULTURE; MORPHOGENESIS; CANCER; LIVER; METABOLISM;
D O I
10.3389/fbioe.2020.00725
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The gastrointestinal (GI) tract is a complex system responsible for nutrient absorption, digestion, secretion, and elimination of waste products that also hosts immune surveillance, the intestinal microbiome, and interfaces with the nervous system. Traditionalin vitrosystems cannot harness the architectural and functional complexity of the GI tract. Recent advances in organoid engineering, microfluidic organs-on-a-chip technology, and microfabrication allows us to create betterin vitromodels of human organs/tissues. These micro-physiological systems could integrate the numerous cell types involved in GI development and physiology, including intestinal epithelium, endothelium (vascular), nerve cells, immune cells, and their interplay/cooperativity with the microbiome. In this review, we report recent progress in developing micro-physiological models of the GI systems. We also discuss how these models could be used to study normal intestinal physiology such as nutrient absorption, digestion, and secretion as well as GI infection, inflammation, cancer, and metabolism.
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页数:17
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