Literature DB >> 8745335

Culture matrix configuration and composition in the maintenance of hepatocyte polarity and function.

P V Moghe1, F Berthiaume, R M Ezzell, M Toner, R G Tompkins, M L Yarmush.   

Abstract

Several extracellular matrix (ECM) configurations involving type I collagen and Matrigel were examined for their ability to support differentiated function and polarity of cultured adult rat hepatocytes. Collagen sandwich- and Matrigel-based cultures yielded superior and comparable albumin secretion for at least 2 weeks. In collagen sandwich, hepatocytes were polygonal, and formed multicellular arrays. Collagen sandwich was also found to promote in vivo-like polarization of F-actin, cell adhesion molecules (E-cadherin), and lateral (Na+, K(+)-ATPase, glucose transporter) and apical (dipeptidyl peptidase, aminopeptidase) membrane polarity markers, but not the expression of the gap junction protein connexin 32 and the epidermal growth factor (EGF) receptor. In contrast, hepatocytes cultured in or on Matrigel were more rounded and formed aggregates. Matrigel-based cultures also elicited detectable levels of connexin and EGF receptor and an altered distribution of F-actin, E-cadherin, and apical and lateral membrane proteins. Composite sandwich configurations containing collagen I and Matrigel restored markers lacking in the collagen sandwich, and showed a variable morphology and membrane polarity. Hepatocyte polarity could thus be manipulated by the overall ECM composition. Furthermore, in composite sandwich cultures, these manipulations can be effected largely independent of changes in hepatocyte morphology and albumin secretion.

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Year:  1996        PMID: 8745335     DOI: 10.1016/0142-9612(96)85576-1

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  51 in total

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4.  A comparative study of genome-wide transcriptional profiles of primary hepatocytes in collagen sandwich and monolayer cultures.

Authors:  Yeonhee Kim; Christopher D Lasher; Logan M Milford; T M Murali; Padmavathy Rajagopalan
Journal:  Tissue Eng Part C Methods       Date:  2010-06-07       Impact factor: 3.056

5.  Development of a quantitative 96-well method to image glycogen storage in primary rat hepatocytes.

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Journal:  Mol Cell Biochem       Date:  2010-03-24       Impact factor: 3.396

6.  Characterization of the secreted proteome of rat hepatocytes cultured in collagen sandwiches.

Authors:  Dora Farkas; Vadiraja B Bhat; Saraswathi Mandapati; John S Wishnok; Steven R Tannenbaum
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7.  Rho kinase, myosin-II, and p42/44 MAPK control extracellular matrix-mediated apical bile canalicular lumen morphogenesis in HepG2 cells.

Authors:  Hilde Herrema; Dominika Czajkowska; Delphine Théard; Johanna M van der Wouden; Dharamdajal Kalicharan; Behnam Zolghadr; Dick Hoekstra; Sven C D van Ijzendoorn
Journal:  Mol Biol Cell       Date:  2006-05-10       Impact factor: 4.138

8.  Gene expression profiling of extracellular matrix as an effector of human hepatocyte phenotype in primary cell culture.

Authors:  Jeanine L Page; Mary C Johnson; Katy M Olsavsky; Steven C Strom; Helmut Zarbl; Curtis J Omiecinski
Journal:  Toxicol Sci       Date:  2007-02-27       Impact factor: 4.849

9.  Long-term culture and coculture of primary rat and human hepatocytes.

Authors:  Maria Shulman; Yaakov Nahmias
Journal:  Methods Mol Biol       Date:  2013

10.  Osteogenic and angiogenic potentials of monocultured and co-cultured human-bone-marrow-derived mesenchymal stem cells and human-umbilical-vein endothelial cells on three-dimensional porous beta-tricalcium phosphate scaffold.

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Journal:  Acta Biomater       Date:  2012-08-16       Impact factor: 8.947

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