Extended proliferation of chicken‐ and Okinawa rail‐derived fibroblasts by expression of cell cycle regulators. Issue 5 (11th November 2018)

• Record Type: Journal Article
• Authors: Katayama, Masafumi; Kiyono, Tohru; Ohmaki, Hitomi; Eitsuka, Takahiro; Endoh, Daiji; Inoue‐Murayama, Miho; Nakajima, Nobuyoshi; Onuma, Manabu; Fukuda, Tomokazu
• Is Part Of: Journal of cellular physiology. Volume 234:Issue 5(2019:May)
• Page Start: 6709
• Page End: 6720
• Publication Date: 2018-11-11
• Subjects: avian -- cell cycle -- cellular senescence -- endangered animal -- immortalized cell; Physiology -- Periodicals; Cell physiology -- Periodicals; 571.6
• DOI: 10.1002/jcp.27417
• Languages: English
• ISSNs: 0021-9541

Abstract

Abstract: 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 introduced the simian virus 40 T antigen ( SV40T) and human papillomavirus (HPV)‐E6E7 to chick and Okinawa rail (endangered species)derived fibroblast. As a result, neither the SV40T nor E6E7 genes could induce avian cell immortality. Accordingly, we attempted to use a recently developed immortalization method, which involved the coexpression of mutant cyclin‐dependent kinase 4 (CDK4), Cyclin D, and TERT (K4DT method) in these avian cells. Although the K4DT method could not efficiently induce the efficient immortalization in mass cell population, cellular division until the senescence was significantly extended by K4DT, we succeeded to obtain the immortalized avian cells (chick K4DT: one clone, Okinawa rail K4DT: three clones, Okinawa rail K4DT + telomerase RNA component: one clone) with K4DT expression. We conclude that K4DT expression is used to extend the cell division and immortalization of avian‐derived cells.