Increased expression of hras induces early, but not full, senescence in the immortal fish cell line, EPC

In contrast to most mammals including human, fish cell lines have long been known to be immortal, with little sign of cellular senescence, despite the absence of transformation. Recently, our laboratory reported that DNA demethylation with 5-aza-2'-deoxycytidine (5-Aza-dC) induces telomere-independent cellular senescence and senescence-associated secretory phenotype (SASP) in an immortal fish cell line, EPC (Epithelioma papulosum cyprini). However, it is not known how fish derived cultured cells are usually resistant to aging in vitro. In this study, we focused on Ras, which carries out the main role of Ras-induced senescence (RIS), and investigated the role of Ras in the regulation of senescence in EPC cells. Our results show that 5-Aza-dC induced the expression of the ras (hras, kras, nras) gene in EPC cells. EPC cells overexpressing HRas or its constitutively active form (HRas(v12)) showed p53-dependent senescence-like growth arrest and senescence-associated beta-galactosidase (SA-beta-gal) activity with a large and/or flat morphology characteristic of cell senescence. On the other hand, the SASP was not induced. These results imply that the increased expression of HRas contributes to early senescence in EPC cells, but it alone may not be sufficient for the full senescence, even if HRas is aberrantly activated. Thus, the limited mechanism of RIS may play a role in the senescence-resistance of fish cell lines.

Automated summary

The study showed that DNA demethylation with 5-Aza-dC can induce senescence in telomere-independent fish cell line EPC. Overexpression of HRas gene contributes to early senescence in EPC cells, but may not be sufficient for full senescence. The limited mechanism of Ras-induced senescence may play a role in the senescence-resistance of fish cell lines.