Robust Formation of an Epithelial Layer of Human Intestinal Organoids in a Polydimethylsiloxane-Based Gut-on-a-Chip Microdevice

被引:17
作者
Shin, Woojung [1 ]
Ambrosini, Yoko M. [1 ]
Shin, Yong Cheol [1 ]
Wu, Alexander [1 ]
Min, Soyoun [1 ]
Koh, Domin [1 ]
Park, Sowon [2 ]
Kim, Seung [2 ]
Koh, Hong [2 ]
Kim, Hyun Jung [1 ,3 ]
机构
[1] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
[2] Yonsei Univ, Severance Hosp, Severance Fecal Microbiota Transplantat Ctr, Dept Pediat,Coll Med, Seoul, South Korea
[3] Univ Texas Austin, Dell Med Sch, Dept Oncol, Austin, TX 78712 USA
来源
FRONTIERS IN MEDICAL TECHNOLOGY | 2020年 / 2卷
基金
新加坡国家研究基金会; 美国国家卫生研究院;
关键词
polydimethylsiloxane; hydrophobicity; surface functionalization; organoids; extracellular matrix; cell attachment; gut-on-a-chip; MICROFLUIDIC DEVICES; IN-VITRO; POLY(DIMETHYLSILOXANE); MICROBIOME; SURFACE; CELLS; POLYETHYLENIMINE; CYTOTOXICITY; CHALLENGES; MECHANISM;
D O I
10.3389/fmedt.2020.00002
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Polydimethylsiloxane (PDMS) is a silicone polymer that has been predominantly used in a human organ-on-a-chip microphysiological system. The hydrophobic surface of a microfluidic channel made of PDMS often results in poor adhesion of the extracellular matrix (ECM) as well as cell attachment. The surface modification by plasma or UV/ozone treatment in a PDMS-based device produces a hydrophilic surface that allows robust ECM coating and the reproducible attachment of human intestinal immortalized cell lines. However, these surface-activating methods have not been successful in forming a monolayer of the biopsy-derived primary organoid epithelium. Several existing protocols to grow human intestinal organoid cells in a PDMS microchannel are not always reproducibly operative due to the limited information. Here, we report an optimized methodology that enables robust and reproducible attachment of the intestinal organoid epithelium in a PDMS-based gut-on-a-chip. Among several reported protocols, we optimized a method by performing polyethyleneimine-based surface functionalization followed by the glutaraldehyde cross linking to activate the PDMS surface. Moreover, we discovered that the post-functionalization step contributes to provide uniform ECM deposition that allows to produce a robust attachment of the dissociated intestinal organoid epithelium in a PDMS-based microdevice. We envision that our optimized protocol may disseminate an enabling methodology to advance the integration of human organotypic cultures in a human organ-on-a-chip for patient-specific disease modeling.
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页数:13
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