Shin Woojung, Ambrosini Yoko M, Shin Yong Cheol, Wu Alexander, Min Soyoun, Koh Domin, Park Sowon, Kim Seung, Koh Hong, Kim Hyun Jung
Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, United States.
Severance Fecal Microbiota Transplantation Center, Severance Hospital, Department of Pediatrics, Yonsei University College of Medicine, Seoul, South Korea.
Front Med Technol. 2020 Aug;2. doi: 10.3389/fmedt.2020.00002. Epub 2020 Aug 7.
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.
聚二甲基硅氧烷(PDMS)是一种有机硅聚合物,主要用于人体芯片上器官的微生理系统。由PDMS制成的微流控通道的疏水表面常常导致细胞外基质(ECM)的粘附性差以及细胞附着困难。在基于PDMS的装置中通过等离子体或紫外线/臭氧处理进行表面改性可产生亲水性表面,从而实现强大的ECM涂层以及人肠道永生化细胞系的可重复附着。然而,这些表面活化方法在形成活检来源的原代类器官上皮单层方面并不成功。由于信息有限,现有的几种在PDMS微通道中培养人肠道类器官细胞的方案并不总是能够可重复地操作。在此,我们报告了一种优化方法,该方法能够在基于PDMS的肠道芯片中实现肠道类器官上皮的强大且可重复的附着。在几种已报道的方案中,我们通过基于聚乙烯亚胺的表面功能化,随后进行戊二醛交联以活化PDMS表面,优化了一种方法。此外,我们发现功能化后步骤有助于提供均匀的ECM沉积,从而能够在基于PDMS的微装置中实现解离的肠道类器官上皮的强大附着。我们设想,我们优化的方案可能会传播一种促进人体芯片上器官中人体器官型培养物整合以进行患者特异性疾病建模的可行方法。