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dc.contributor.authorJiang, L
dc.contributor.authorIvich, F
dc.contributor.authorTahsin, S
dc.contributor.authorTran, M
dc.contributor.authorFrank, S B
dc.contributor.authorMiranti, C K
dc.contributor.authorZohar, Y
dc.date.accessioned2020-02-01T01:58:13Z
dc.date.available2020-02-01T01:58:13Z
dc.date.issued2019-11-20
dc.identifier.citationJiang, L., Ivich, F., Tahsin, S., Tran, M., Frank, S. B., Miranti, C. K., & Zohar, Y. (2019). Human stroma and epithelium co-culture in a microfluidic model of a human prostate gland. Biomicrofluidics, 13(6), 064116.en_US
dc.identifier.issn1932-1058
dc.identifier.pmid31768202
dc.identifier.doi10.1063/1.5126714
dc.identifier.urihttp://hdl.handle.net/10150/636861
dc.description.abstractThe prostate is a walnut-sized gland that surrounds the urethra of males at the base of the bladder comprising a muscular portion, which controls the release of urine, and a glandular portion, which secretes fluids that nourish and protect sperms. Here, we report the development of a microfluidic-based model of a human prostate gland. The polydimethylsiloxane (PDMS) microfluidic device, consisting of two stacked microchannels separated by a polyester porous membrane, enables long-term in vitro cocultivation of human epithelial and stromal cells. The porous separation membrane provides an anchoring scaffold for long-term culturing of the two cell types on its opposite surfaces allowing paracrine signaling but not cell crossing between the two channels. The microfluidic device is transparent enabling high resolution bright-field and fluorescence imaging. Within this coculture model of a human epithelium/stroma interface, we simulated the functional development of the in vivo human prostate gland. We observed the successful differentiation of basal epithelial cells into luminal secretory cells determined biochemically by immunostaining with known differentiation biomarkers, particularly androgen receptor expression. We also observed morphological changes where glandlike mounds appeared with relatively empty centers reminiscent of prostatic glandular acini structures. This prostate-on-a-chip will facilitate the direct evaluation of paracrine and endocrine cross talk between these two cell types as well as studies associated with normal vs disease-related events such as prostate cancer.en_US
dc.description.sponsorshipUniversity of Arizonaen_US
dc.language.isoenen_US
dc.publisherAMER INST PHYSICSen_US
dc.rightsCopyright © 2019 Author(s). Published under license by AIP Publishing.en_US
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.titleHuman stroma and epithelium co-culture in a microfluidic model of a human prostate glanden_US
dc.typeArticleen_US
dc.contributor.departmentUniv Arizona, Dept Aerosp & Mech Engnen_US
dc.contributor.departmentUniv Arizona, Dept Biomed Engnen_US
dc.contributor.departmentUniv Arizona, Dept Cellular & Mol Meden_US
dc.contributor.departmentUniv Arizona, Arizona Canc Ctren_US
dc.identifier.journalBIOMICROFLUIDICSen_US
dc.description.note12 month embargo; published online: 20 November 2019en_US
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en_US
dc.eprint.versionFinal published versionen_US
dc.source.journaltitleBiomicrofluidics
dc.source.volume13
dc.source.issue6
dc.source.beginpage064116
dc.source.endpage
dc.source.countryUnited States


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