<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22</volume><submitter>Seidemann L</submitter><pubmed_abstract>Loss of differentiation of primary human hepatocytes (PHHs) &lt;i>ex vivo&lt;/i> is a known problem of &lt;i>in vitro&lt;/i> liver models. Culture optimizations using collagen type I and Matrigel reduce the dedifferentiation process but are not able to prevent it. While neither of these extracellular matrices (ECMs) on their own correspond to the authentic hepatic ECM, a combination of them could more closely resemble the &lt;i>in vivo&lt;/i> situation. Our study aimed to systematically analyze the influence of mixed matrices composed of collagen type I and Matrigel on the maintenance and reestablishment of hepatic functions. Therefore, PHHs were cultured on mixed collagen-Matrigel matrices in monolayer and sandwich cultures and viability, metabolic capacity, differentiation markers, cellular arrangement an</pubmed_abstract><journal>EXCLI journal</journal><pagination>12-34</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9837384</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Optimization of extracellular matrix for primary human hepatocyte cultures using mixed collagen-Matrigel matrices.</pubmed_title><pmcid>PMC9837384</pmcid><pubmed_authors>Prinz S</pubmed_authors><pubmed_authors>Scherbel JC</pubmed_authors><pubmed_authors>Damm G</pubmed_authors><pubmed_authors>Seehofer D</pubmed_authors><pubmed_authors>Gotz C</pubmed_authors><pubmed_authors>Seidemann L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimization of extracellular matrix for primary human hepatocyte cultures using mixed collagen-Matrigel matrices.</name><description>Loss of differentiation of primary human hepatocytes (PHHs) &lt;i>ex vivo&lt;/i> is a known problem of &lt;i>in vitro&lt;/i> liver models. Culture optimizations using collagen type I and Matrigel reduce the dedifferentiation process but are not able to prevent it. While neither of these extracellular matrices (ECMs) on their own correspond to the authentic hepatic ECM, a combination of them could more closely resemble the &lt;i>in vivo&lt;/i> situation. Our study aimed to systematically analyze the influence of mixed matrices composed of collagen type I and Matrigel on the maintenance and reestablishment of hepatic functions. Therefore, PHHs were cultured on mixed collagen-Matrigel matrices in monolayer and sandwich cultures and viability, metabolic capacity, differentiation markers, cellular arrangement an</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T11:10:36.359Z</modification><creation>2025-04-04T11:10:36.359Z</creation></dates><accession>S-EPMC9837384</accession><cross_references><pubmed>36660192</pubmed><doi>10.17179/excli2022-5459</doi></cross_references></HashMap>