Establishment of the immortalized cell line derived from Okinawa rail (endangered species)

As part of the cellular conservation of endangered avian species, our group initiated a primary cell culture project aimed at preserving endangered avian species in Japan, such as the Okinawa rail. However, primary cells cannot be cultured indefinitely because of cellular senescence and stresses caused by cell culture. To overcome these cell culture limitations, primary cells have to be immortalized. Although immortalized cultured cells are useful for various functional assays or transcriptome analysis, highly efficient and reproducible immortalization methods have not been developed in avian-derived cells. We firstly introduced the simian Virus 40T antigen (SV40T) and human papillomavirus (HPV)-E6E7 to chick and Okinawa rail (endangered species) derived fibroblast. However, neither the SV40T nor E6E7 genes could induce avian cell immortality.

Accordingly, we attempted to use a recently developed immortalization method, which involves the co-expression of mutant CDK4, Cyclin D and TERT (K4DT method) in these avian cells. Cellular division until the senescence was significantly extended by K4DT although the K4DT method could not induce the efficient immortalization in mass cell population. As a result, we succeeded to obtain the immortalized avian cells with K4DT expression. We conclude that the K4DT method is useful to extend the cell division and immortalization of avian-derived cells.