Evaluation of the metabolic capability of primary human hepatocytes in three‐dimensional cultures on microstructural plates

摘要

Abstract The NanoCulture Plate (NCP) is a novel microstructural plate designed as a base for the three‐dimensional culture of cells/tissues. This study examined whether or not the metabolic capability of human primary hepatocytes is well maintained during culture on NCPs. The hepatocytes formed aggregates after seeding and their ATP content was well maintained during culture for 21?days. Expression of CYP1A2, 2B6, 2C9, 2C19, 2D6, 2E1 and 3A4 mRNAs was detected throughout the 21‐day culture period. Addition of CYP substrate drugs (midazolam, diclofenac, lamotrigine and acetaminophen) resulted in the formation of multiple metabolites with a corresponding decrease in the amounts of the unchanged compounds. The inducers omeprazole, phenobarbital and rifampicin increased the levels of CYP1A2, 2B6 and 3A4 mRNAs by 110‐fold, 12.5‐fold and 5.4‐fold, respectively, at day 2, compared with control human hepatocytes. CYP activities were also increased at 2?days after inducer treatment (CYP1A2, 2.2‐fold; CYP2B6, 20.6‐fold; CYP3A4, 3.3‐fold). The results indicate that the hepatocyte spheroids on NCP have detectable and inducible metabolic abilities during the 7‐day culture period.