TY - JOUR
T1 - Human Colon-on-a-Chip Enables Continuous In Vitro Analysis of Colon Mucus Layer Accumulation and Physiology
AU - Sontheimer-Phelps, Alexandra
AU - Chou, David B.
AU - Tovaglieri, Alessio
AU - Ferrante, Thomas C.
AU - Duckworth, Taylor
AU - Fadel, Cicely
AU - Frismantas, Viktoras
AU - Sutherland, Arlene D.
AU - Jalili-Firoozinezhad, Sasan
AU - Kasendra, Magdalena
AU - Stas, Eric
AU - Weaver, James C.
AU - Richmond, Camilla A.
AU - Levy, Oren
AU - Prantil-Baun, Rachelle
AU - Breault, David T.
AU - Ingber, Donald E.
N1 - Publisher Copyright:
© 2020 The Authors
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Background & Aims: The mucus layer in the human colon protects against commensal bacteria and pathogens, and defects in its unique bilayered structure contribute to intestinal disorders, such as ulcerative colitis. However, our understanding of colon physiology is limited by the lack of in vitro models that replicate human colonic mucus layer structure and function. Here, we investigated if combining organ-on-a-chip and organoid technologies can be leveraged to develop a human-relevant in vitro model of colon mucus physiology. Methods: A human colon-on-a-chip (Colon Chip) microfluidic device lined by primary patient-derived colonic epithelial cells was used to recapitulate mucus bilayer formation, and to visualize mucus accumulation in living cultures noninvasively. Results: The Colon Chip supports spontaneous goblet cell differentiation and accumulation of a mucus bilayer with impenetrable and penetrable layers, and a thickness similar to that observed in the human colon, while maintaining a subpopulation of proliferative epithelial cells. Live imaging of the mucus layer formation on-chip showed that stimulation of the colonic epithelium with prostaglandin E2, which is increased during inflammation, causes rapid mucus volume expansion via an Na-K-Cl cotransporter 1 ion channel–dependent increase in its hydration state, but no increase in de novo mucus secretion. Conclusions: This study shows the production of colonic mucus with a physiologically relevant bilayer structure in vitro, which can be analyzed in real time noninvasively. The Colon Chip may offer a new preclinical tool to analyze the role of mucus in human intestinal homeostasis as well as diseases, such as ulcerative colitis and cancer.
AB - Background & Aims: The mucus layer in the human colon protects against commensal bacteria and pathogens, and defects in its unique bilayered structure contribute to intestinal disorders, such as ulcerative colitis. However, our understanding of colon physiology is limited by the lack of in vitro models that replicate human colonic mucus layer structure and function. Here, we investigated if combining organ-on-a-chip and organoid technologies can be leveraged to develop a human-relevant in vitro model of colon mucus physiology. Methods: A human colon-on-a-chip (Colon Chip) microfluidic device lined by primary patient-derived colonic epithelial cells was used to recapitulate mucus bilayer formation, and to visualize mucus accumulation in living cultures noninvasively. Results: The Colon Chip supports spontaneous goblet cell differentiation and accumulation of a mucus bilayer with impenetrable and penetrable layers, and a thickness similar to that observed in the human colon, while maintaining a subpopulation of proliferative epithelial cells. Live imaging of the mucus layer formation on-chip showed that stimulation of the colonic epithelium with prostaglandin E2, which is increased during inflammation, causes rapid mucus volume expansion via an Na-K-Cl cotransporter 1 ion channel–dependent increase in its hydration state, but no increase in de novo mucus secretion. Conclusions: This study shows the production of colonic mucus with a physiologically relevant bilayer structure in vitro, which can be analyzed in real time noninvasively. The Colon Chip may offer a new preclinical tool to analyze the role of mucus in human intestinal homeostasis as well as diseases, such as ulcerative colitis and cancer.
KW - Goblet Cell
KW - Inflammatory Bowel Disease
KW - Intestine
KW - Microfluidic
KW - Organ Chip
KW - Organoid
UR - http://www.scopus.com/inward/record.url?scp=85079665015&partnerID=8YFLogxK
U2 - 10.1016/j.jcmgh.2019.11.008
DO - 10.1016/j.jcmgh.2019.11.008
M3 - Article
C2 - 31778828
AN - SCOPUS:85079665015
SN - 2352-345X
VL - 9
SP - 507
EP - 526
JO - CMGH
JF - CMGH
IS - 3
ER -