Mitogenic signalling and the p16INK4a-Rb pathway cooperate to enforce irreversible cellular senescence

Akiko Takahashi, Naoko Ohtani, Kimi Yamakoshi, Shin Ichi Iida, Hidetoshi Tahara, Keiko Nakayama, Keiichi I. Nakayama, Toshinori Ide, Hideyuki Saya, Eiji Hara

研究成果: Article査読

343 被引用数 (Scopus)

抄録

The p16INK4a cyclin-dependent kinase inhibitor has a key role in establishing stable G1 cell-cycle arrest through activating the retinoblastoma (Rb) tumour suppressor protein pRb1-5 in cellular senescence. Here, we show that the p16INK4a/ Rb-pathway also cooperates with mitogenic signals to induce elevated intracellular levels of reactive oxygen species (ROS), thereby activating protein kinase Cδ (PKCδ) in human senescent cells. Importantly, once activated by ROS, PKCδ promotes further generation of ROS, thus establishing a positive feedback loop to sustain ROS-PKCδ signalling6-8. Sustained activation of ROS-PKCδ signalling irreversibly blocks cytokinesis, at least partly through reducing the level of WARTS (also known as LATS1), a mitotic exit network (MEN) kinase required for cytokinesis9-11, in human senescent cells. This irreversible cytokinetic block is likely to act as a second barrier to cellular immortalization ensuring stable cell-cycle arrest in human senescent cells. These results uncover an unexpected role for the p16INK4a-Rb pathway and provide a new insight into how senescent cell-cycle arrest is enforced in human cells.

本文言語English
ページ(範囲)1291-1297
ページ数7
ジャーナルNature Cell Biology
8
11
DOI
出版ステータスPublished - 11-2006
外部発表はい

All Science Journal Classification (ASJC) codes

  • 細胞生物学

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