Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/90298
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dc.contributor.authorBrown, Jessica H.en
dc.contributor.authorDas, Prativaen
dc.contributor.authorDiVito, Michael D.en
dc.contributor.authorIvancic, Daviden
dc.contributor.authorTan, Lay Pohen
dc.contributor.authorWertheim, Jason A.en
dc.date.accessioned2019-05-30T02:46:28Zen
dc.date.accessioned2019-12-06T17:45:10Z-
dc.date.available2019-05-30T02:46:28Zen
dc.date.available2019-12-06T17:45:10Z-
dc.date.issued2018en
dc.identifier.citationBrown, J. H., Das, P., DiVito, M. D., Ivancic, D., Tan, L. P., & Wertheim, J. A. (2018). Nanofibrous PLGA electrospun scaffolds modified with type I collagen influence hepatocyte function and support viability in vitro. Acta Biomaterialia, 73, 217-227. doi:10.1016/j.actbio.2018.02.009en
dc.identifier.issn1742-7061en
dc.identifier.urihttps://hdl.handle.net/10356/90298-
dc.identifier.urihttp://hdl.handle.net/10220/48478en
dc.description.abstractA major challenge of maintaining primary hepatocytes in vitro is progressive loss of hepatocyte-specific functions, such as protein synthesis and cytochrome P450 (CYP450) catalytic activity. We developed a three-dimensional (3D) nanofibrous scaffold made from poly(l-lactide-co-glycolide) (PLGA) polymer using a newly optimized wet electrospinning technique that resulted in a highly porous structure that accommodated inclusion of primary human hepatocytes. Extracellular matrix (ECM) proteins (type I collagen or fibronectin) at varying concentrations were chemically linked to electrospun PLGA using amine coupling to develop an in vitro culture system containing the minimal essential ECM components of the liver micro-environment that preserve hepatocyte function in vitro. Cell-laden nanofiber scaffolds were tested in vitro to maintain hepatocyte function over a two-week period. Incorporation of type I collagen onto PLGA scaffolds (PLGA-Chigh: 100 µg/mL) led to 10-fold greater albumin secretion, 4-fold higher urea synthesis, and elevated transcription of hepatocyte-specific CYP450 genes (CYP3A4, 3.5-fold increase and CYP2C9, 3-fold increase) in primary human hepatocytes compared to the same cells grown within unmodified PLGA scaffolds over two weeks. These indices, measured using collagen-bonded scaffolds, were also higher than scaffolds coupled to fibronectin or an ECM control sandwich culture composed of type I collagen and Matrigel. Induction of CYP2C9 activity was also higher in these same type I collagen PLGA scaffolds compared to other ECM-modified or unmodified PLGA constructs and was equivalent to the ECM control at 7 days. Together, we demonstrate a minimalist ECM-based 3D synthetic scaffold that accommodates primary human hepatocyte inclusion into the matrix, maintains long-term in vitro survival and stimulates function, which can be attributed to coupling of type I collagen.en
dc.format.extent44 p.en
dc.language.isoenen
dc.relation.ispartofseriesActa Biomaterialiaen
dc.rights© 2018 Acta Materialia Inc. All rights reserved. This paper was published by Elsevier Ltd in Acta Biomaterialia and is made available with permission of Acta Materialia Inc.en
dc.subjectTissue Engineeringen
dc.subjectElectrospun Nanofibersen
dc.subjectDRNTU::Engineering::Materialsen
dc.titleNanofibrous PLGA electrospun scaffolds modified with type I collagen influence hepatocyte function and support viability in vitroen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Materials Science and Engineeringen
dc.contributor.schoolInterdisciplinary Graduate School (IGS)en
dc.identifier.doihttp://dx.doi.org/10.1016/j.actbio.2018.02.009en
dc.description.versionAccepted versionen
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