Dnmt1-dependent Chk1 pathway suppression is protective against neuron division

被引:8
|
作者
Oshikawa, Mio [1 ]
Okada, Kei [1 ]
Tabata, Hidenori [2 ]
Nagata, Koh-ichi [2 ]
Ajioka, Itsuki [1 ,3 ]
机构
[1] TMDU, CBIR, Tokyo 1138510, Japan
[2] Aichi Human Serv Ctr, Inst Dev Res, Dept Mol Neurobiol, Kasugai, Aichi 4800392, Japan
[3] Japan Sci & Technol Agcy JST, Precursory Res Embryon Sci & Technol PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan
来源
DEVELOPMENT | 2017年 / 144卷 / 18期
基金
日本科学技术振兴机构;
关键词
Cell cycle; Cerebral cortical neurons; Stroke; Chk1; Dnmt1; Retinoblastoma proteins; CELL-CYCLE REGULATION; RETINOBLASTOMA PROTEIN; THERAPEUTIC TARGET; ECTOPIC EXPRESSION; S-PHASE; RB; DEATH; KINASE; PROLIFERATION; CHECKPOINT;
D O I
10.1242/dev.154013
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neuronal differentiation and cell-cycle exit are tightly coordinated, even in pathological situations. When pathological neurons re-enter the cell cycle and progress through the S phase, they undergo cell death instead of division. However, the mechanisms underlying mitotic resistance are mostly unknown. Here, we have found that acute inactivation of retinoblastoma (Rb) family proteins (Rb, p107 and p130) in mouse postmitotic neurons leads to cell death after S-phase progression. Checkpoint kinase 1 (Chk1) pathway activation during the S phase prevented the cell death, and allowed the division of cortical neurons that had undergone acute Rb family inactivation, oxygen-glucose deprivation (OGD) or in vivo hypoxia-ischemia. During neurogenesis, cortical neurons became protected from S-phase Chk1 pathway activation by the DNA methyltransferase Dnmt1, and underwent cell death after S-phase progression. Our results indicate that Chk1 pathway activation overrides mitotic safeguards and uncouples neuronal differentiation from mitotic resistance.
引用
收藏
页码:3303 / 3314
页数:12
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