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dc.contributor.authorZhang, Jianbo
dc.contributor.authorHuang, Yu-Ja
dc.contributor.authorYoon, Jun Young
dc.contributor.authorKemmitt, John
dc.contributor.authorWright, Charles
dc.contributor.authorSchneider, Kirsten
dc.contributor.authorSphabmixay, Pierre
dc.contributor.authorHernandez-Gordillo, Victor
dc.contributor.authorHolcomb, Steven J
dc.contributor.authorBhushan, Brij
dc.contributor.authorRohatgi, Gar
dc.contributor.authorBenton, Kyle
dc.contributor.authorCarpenter, David
dc.contributor.authorKester, Jemila C
dc.contributor.authorEng, George
dc.contributor.authorBreault, David T
dc.contributor.authorYilmaz, Omer
dc.contributor.authorTaketani, Mao
dc.contributor.authorVoigt, Christopher A
dc.contributor.authorCarrier, Rebecca L
dc.contributor.authorTrumper, David L
dc.contributor.authorGriffith, Linda G
dc.date.accessioned2021-10-27T19:52:36Z
dc.date.available2021-10-27T19:52:36Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/133396
dc.description.abstractBackground: The gut microbiome plays an important role in human health and disease. Gnotobiotic animal and in vitro cell-based models provide some informative insights into mechanistic crosstalk. However, there is no existing system for a long-term co-culture of a human colonic mucosal barrier with super oxygen-sensitive commensal microbes, hindering the study of human-microbe interactions in a controlled manner. Methods: Here, we investigated the effects of an abundant super oxygen-sensitive commensal anaerobe, Faecalibacterium prausnitzii, on a primary human mucosal barrier using a Gut-MIcrobiome (GuMI) physiome platform that we designed and fabricated. Findings: Long-term continuous co-culture of F. prausnitzii for two days with colon epithelia, enabled by continuous flow of completely anoxic apical media and aerobic basal media, resulted in a strictly anaerobic apical environment fostering growth of and butyrate production by F. prausnitzii, while maintaining a stable colon epithelial barrier. We identified elevated differentiation and hypoxia-responsive genes and pathways in the platform compared with conventional aerobic static culture of the colon epithelia, attributable to a combination of anaerobic environment and continuous medium replenishment. Furthermore, we demonstrated anti-inflammatory effects of F. prausnitzii through HDAC and the TLR-NFKB axis. Finally, we identified that butyrate largely contributes to the anti-inflammatory effects by downregulating TLR3 and TLR4. Conclusions: Our results are consistent with some clinical observations regarding F. prausnitzii, thus motivating further studies employing this platform with more complex engineered colon tissues for understanding the interaction between the human colonic mucosal barrier and microbiota, pathogens, or engineered bacteria.
dc.language.isoen
dc.publisherElsevier BV
dc.relation.isversionof10.1016/J.MEDJ.2020.07.001
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs License
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceElsevier
dc.titlePrimary Human Colonic Mucosal Barrier Crosstalk with Super Oxygen-Sensitive Faecalibacterium prausnitzii in Continuous Culture
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.contributor.departmentMassachusetts Institute of Technology. Center for Gynepathology Research
dc.relation.journalMed
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-08-05T15:03:27Z
dspace.orderedauthorsZhang, J; Huang, Y-J; Yoon, JY; Kemmitt, J; Wright, C; Schneider, K; Sphabmixay, P; Hernandez-Gordillo, V; Holcomb, SJ; Bhushan, B; Rohatgi, G; Benton, K; Carpenter, D; Kester, JC; Eng, G; Breault, DT; Yilmaz, O; Taketani, M; Voigt, CA; Carrier, RL; Trumper, DL; Griffith, LG
dspace.date.submission2021-08-05T15:03:30Z
mit.journal.volume2
mit.journal.issue1
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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