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pubmed-article:16719396pubmed:dateCreated2006-5-24lld:pubmed
pubmed-article:16719396pubmed:abstractTextMimicking the in vivo microenvironment is one of the current strategies to maintain liver-specific functionality in primary cultured hepatocytes for long periods. Freshly isolated hepatocytes entrapped in collagen gel type I (collagen gel immobilization culture) or sandwiched between two layers of hydrated collagen type I (collagen gel sandwich culture) are known to display liver-specific functions (e.g., biotransformation capacity) for more than 6 wk. We describe how to set up both types of organotypical hepatocyte culture systems. Besides a detailed protocol, we give some practical tips, taken from our own experience with long-term hepatocyte culture.lld:pubmed
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pubmed-article:16719396pubmed:authorpubmed-author:RogiersVeraVlld:pubmed
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pubmed-article:16719396pubmed:authorpubmed-author:VinkenMathieu...lld:pubmed
pubmed-article:16719396pubmed:authorpubmed-author:SnykersSarahSlld:pubmed
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pubmed-article:16719396pubmed:volume320lld:pubmed
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pubmed-article:16719396pubmed:pagination247-54lld:pubmed
pubmed-article:16719396pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:16719396pubmed:year2006lld:pubmed
pubmed-article:16719396pubmed:articleTitleRat hepatocyte cultures: collagen gel sandwich and immobilization cultures.lld:pubmed
pubmed-article:16719396pubmed:affiliationDepartment of Toxicology, Vrije Universiteit Brussel, Belgium.lld:pubmed
pubmed-article:16719396pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16719396pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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