Fluid shear stress enhances differentiation of jejunal human enteroids in Intestine-Chip

• Published in: American journal of physiology: Gastrointestinal and liver physiology 2021-03, Vol.320 (3), p.G258-G271
• Main Authors: Yin, Jianyi, Sunuwar, Laxmi, Kasendra, Magdalena, Yu, Huimin, Tse, Chung-Ming, Talbot, Jr, C Conover, Boronina, Tatiana, Cole, Robert, Karalis, Katia, Donowitz, Mark
• Format: Article
• Language: English
• Subjects: Adult; Apoptosis; Carrier Proteins - metabolism; Cell Differentiation; Cells, Cultured; Enterocytes - cytology; Enterocytes - metabolism; Female; Human Umbilical Vein Endothelial Cells - metabolism; Humans; Jejunum - cytology; Jejunum - metabolism; Lithostathine - metabolism; Microfluidics - methods; Primary Cell Culture - methods; Solute Carrier Family 12, Member 2 - metabolism; Stress, Mechanical; Thrombospondins - metabolism; Wnt3A Protein - metabolism
• ISSN: 0193-1857; 1522-1547
• DOI: 10.1152/ajpgi.00282.2020

There is increasing evidence that the study of normal human enteroids duplicates many known aspects of human intestinal physiology. However, this epithelial cell-only model lacks the many nonepithelial intestinal cells present in the gastrointestinal tract and exposure to the mechanical forces to which the intestine is exposed. We tested the hypothesis that physical shear forces produced by luminal and blood flow would provide an intestinal model more closely resembling normal human jejunum. Jejunal enteroid monolayers were studied in the Emulate, Inc. Intestine-Chip under conditions of constant luminal and basolateral flow that was designed to mimic normal intestinal fluid flow, with human umbilical vein endothelial cells (HUVECs) on the basolateral surface and with Wnt3A, R-spondin, and Noggin only on the luminal surface. The jejunal enteroids formed monolayers that remained confluent for 6-8 days, began differentiating at least as early as post plating, and demonstrated continuing differentiation over the entire time of the study, as shown by quantitative real-time polymerase chain reaction and Western blot analysis. Differentiation impacted villus genes and proteins differently with early expression of regenerating family member 1α (REG1A), early reduction to a low but constant level of expression of Na -K -2Cl cotransporter 1 (NKCC1), and increasing expression of sucrase-isomaltase (SI) and downregulated in adenoma (DRA). These results were consistent with continual differentiation, as was shown to occur in mouse villus enterocytes. Compared with differentiated enteroid monolayers grown on Transwell inserts, enteroids exposed to flow were more differentiated but exhibited increased apoptosis and reduced carbohydrate metabolism, as shown by proteomic analysis. This study of human jejunal enteroids-on-chip suggests that luminal and basolateral flow produce a model of continual differentiation over time and NaCl absorption that mimics normal intestine and should provide new insights in intestinal physiology. This study showed that polarized enteroid models in which there is no basolateral Wnt3a, are differentiated, regardless of the Wnt3a status of the apical media. The study supports the concept that in the human intestine villus differentiation is not an all or none phenomenon, demonstrating that at different days after lack of basolateral Wnt exposure, clusters of genes and proteins exist geographically along the villus with different domains having d