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https://doi.org/10.1039/B915147H
Title: | Towards a human-on-chip: Culturing multiple cell types on a chip with compartmentalized microenvironments | Authors: | Zhang, Chi Zhao, Ziqing Rahim, Nur Aida Abdul van Noort, Danny Yu, Hanry |
Keywords: | Science & Technology Life Sciences & Biomedicine Physical Sciences Technology Biochemical Research Methods Chemistry, Multidisciplinary Chemistry, Analytical Nanoscience & Nanotechnology Instruments & Instrumentation Biochemistry & Molecular Biology Chemistry Science & Technology - Other Topics MICROFLUIDIC CHANNELS SPECIES-DIFFERENCES HEPATOCYTE CULTURE DRUG DISCOVERY LUNG-CANCER TOXICITY SYSTEM RAT PHARMACOKINETICS ENVIRONMENT |
Issue Date: | 1-Jan-2009 | Publisher: | ROYAL SOC CHEMISTRY | Citation: | Zhang, Chi, Zhao, Ziqing, Rahim, Nur Aida Abdul, van Noort, Danny, Yu, Hanry (2009-01-01). Towards a human-on-chip: Culturing multiple cell types on a chip with compartmentalized microenvironments. LAB ON A CHIP 9 (22) : 3185-3192. ScholarBank@NUS Repository. https://doi.org/10.1039/B915147H | Abstract: | We have developed a multi-channel 3D microfluidic cell culture system (multi-channel 3D-FCCS) with compartmentalized microenvironments for potential application in human drug screening. To this end, the multi-channel 3D-FCCS was designed for culturing different 3D cellular aggregates simultaneously to mimic multiple organs in the body. Four human cell types (C3A, A549, HK-2 and HPA) were chosen to represent the liver, lung, kidney and the adipose tissue, respectively. Cellular functions were optimized by supplementing the common medium with growth factors. However, TGF-β1 was found to enhance A549 functions but inhibit C3A functions. Therefore, TGF-β1 was specifically controlled-released inside the A549 compartment by means of gelatin microspheres mixed with cells, thus creating a cell-specific microenvironment. The function of A549 cells was enhanced while the functions of C3A, HK-2 and HPA cells were uncompromised, demonstrating the limited cross-talk between cell culture compartments similar to the in vivo situation. Such a multi-channel 3D-FCCS could be potentially used to supplement or even replace animal models in drug screening. © 2009 The Royal Society of Chemistry. | Source Title: | LAB ON A CHIP | URI: | https://scholarbank.nus.edu.sg/handle/10635/173665 | ISSN: | 14730197 14730189 |
DOI: | 10.1039/B915147H |
Appears in Collections: | Staff Publications Elements |
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