| Literature DB >> 30247461 |
Yasumasa Mashimo1, Momoko Yoshioka2, Yumie Tokunaga2, Christopher Fockenberg2, Shiho Terada2, Yoshie Koyama2, Teiko Shibata-Seki3, Koki Yoshimoto2, Risako Sakai2, Hayase Hakariya2, Li Liu2, Toshihiro Akaike4, Eiry Kobatake3, Siew-Eng How5, Motonari Uesugi6, Yong Chen7, Ken-Ichiro Kamei8.
Abstract
Cellular microenvironments consist of a variety of cues, such as growth factors, extracellular matrices, and intercellular interactions. These cues are well orchestrated and are crucial in regulating cell functions in a living system. Although a number of researchers have attempted to investigate the correlation between environmental factors and desired cellular functions, much remains unknown. This is largely due to the lack of a proper methodology to mimic such environmental cues in vitro, and simultaneously test different environmental cues on cells. Here, we report an integrated platform of microfluidic channels and a nanofiber array, followed by high-content single-cell analysis, to examine stem cell phenotypes altered by distinct environmental factors. To demonstrate the application of this platform, this study focuses on the phenotypes of self-renewing human pluripotent stem cells (hPSCs). Here, we present the preparation procedures for a nanofiber array and the microfluidic structure in the fabrication of a Multiplexed Artificial Cellular MicroEnvironment (MACME) array. Moreover, overall steps of the single-cell profiling, cell staining with multiple fluorescent markers, multiple fluorescence imaging, and statistical analyses, are described.Entities:
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Year: 2018 PMID: 30247461 PMCID: PMC6235102 DOI: 10.3791/57377
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355