We developed a multi-stage microfluidic technology to derive mature cells from pluripotent cells. This technology was implemented with generation

of 1 mm (diameter of hepatic lobule) stable oxygen gradient. Obtained cells have been characterized both with hepatic markers (AFP, CK 18 −19, ALB, CYP3A) and functional tests (proliferation, glycogen storage, indocyanine green uptake, albumin secretion). Results: We developed a microfluidic technology to generate a stable 〇2 gradient and culture and differentiate human pluripotent cells. We efficiently differentiated both hESCs and hiPSCs. Two hepatic lineages were obtained: hepatocyte- and cholangiocyte-like KU-60019 solubility dmso Aloxistatin chemical structure cells showing high CYP3A expression, ICG uptake, glycogen storage and albumin secretion over a 14-day period. This

technology allowed to accurately control hPSC expansion and fate toward early endoderm commitment, hepatic development and functional maturation on a chip. Compared to conventional culture, microfluidic oxygen-defined platform allowed shortening of the time reguired for differentiation and enhanced functional activity. The proportion between hepatocyte- and cholangiocyte-like cells was 3: 1. In particular, we obtained 75% of cells with glycogen storage capacity, whereas the number of CYP3A-positive cells resulted

in 60% of the total, with 20% increase compared to standard hepatocytes differentiation. Albumin production was about 40% higher than standard conditions. Conclusions: The engineerization of hPSC differentiation into hepatic lineages under defined oxygen gradient will allow us to further understand the mechanisms involved in tissue development. Moreover, mature hepatic cells fully integrated selleck inhibitor on a chip could be directly used for temporaldefined toxicological assays and drug screening. Disclosures: The following people have nothing to disclose: Giovanni G. Giobbe, Federica Tonon, Alessandro Zambon, Federica Michielin, Nicola Elvassore, Annarosa Floreani We have identified the TLR4-NANOG oncogenic pathway in the genesis of CD133+CD49f+ tumor initiating stem cell-like cells (TICs) and liver tumor in alcohol-fed HCV Ns5aTg mice and our most recent finding extends this notion to other HCC models including DEN/Pb-treated or Spnb2+/- mice. Although ectopic TLR4 expression is presumed to have occurred primarily in hepatocytes in these models, the evidence also suggests liver progenitor cells (LPCs) may be the source of TLR4+ TICs. [Aim] The present study investigated whether and why hepatocytes (HC) vs. liver progenitor cells (LPCs) are the primary target of the oncogenic TLR4 pathway.