2B). KUP5 cells exhibited a stable proliferative capacity, as demonstrated by the successful passage at 4–5 days intervals for more than 5 months with a constant population doubling time of approximately 19 h (Fig. 2C). The expression of human c-myc oncogene was confirmed by RT-PCR analysis in KUP5 cells (data not shown). In addition, KUP5 cells can be frozen in a conventional cell-freezing medium. After cryopreservation in liquid nitrogen for 3 years, followed by thawing, KUP5 cells still retained its morphological

properties and stable proliferative capacity (data not shown). The primary Kupffer cells, KUP5, MG6 and BMDM cells were strongly positive for mouse macrophage markers, such as Mac-1 and F4/80 (Fig. 3). Mac-1 and Everolimus research buy F4/80 are cell surface markers, but the antibody–antigen reaction was so intense that the cellular and nuclear structures were difficult to distinguish under a phase contrast microscope. A negative control, rat IgG showed only faint immunostaining (Fig. 3). In addition, multinucleated Epigenetics inhibitor giant cells were occasionally observed in the KUP5 culture (Fig. 3, arrowheads), suggesting that these cells tend to fuse with each other during culture. Multinucleated giant cell formation is associated

with the inflammation associated with macrophages [24], [25] and [26], including Kupffer cells [27]. These results suggest that KUP5 cells have the typical biological properties of macrophages, i. e. Kupffer cells Cyclic nucleotide phosphodiesterase or their precursors, and proliferated in the mixed primary culture of mouse liver cells. Using the same retroviral vector, we previously established microglial cell lines from a C57BL/6 mouse strain (MG6, deposited at RIKEN, Cell Bank, RCB2403) [18], as well as transgenic and gene-knockout mouse strains [28] and [29].

In addition, this retroviral vector has a capacity for infectivity of mouse bone marrow-derived macrophages in culture [20], suggesting that the present retroviral vector is a powerful tool for immortalizing mouse macrophages. Bioassay revealed that there is no infectious viral particles produced in the culture supernatant of KUP5 cells or other microglial and macrophage cell lines immortalized by the same retroviral vector (data not shown). The primary Kupffer cells, KUP5, MG6 and BMDM cells phagocytosed polystyrene microbeads. The phagocytic activities of the cells were quantitatively demonstrated by FC (Fig. 4), indicating that the proportion of the fluorescence-positive cells increased to more than 95% after 2 h of administration. The levels of phagocytosis did not differ among these cell types. These results demonstrate the substantial phagocytic activity of KUP5 cells, which is a distinctive characteristic of macrophages in the liver [22], [23] and [30].