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乙基亚硝基脲在S期积累后以p53依赖的方式诱导神经祖细胞凋亡。

Ethylnitrosourea induces neural progenitor cell apoptosis after S-phase accumulation in a p53-dependent manner.

作者信息

Katayama Kei-ichi, Ueno Masaki, Yamauchi Hirofumi, Nagata Takayuki, Nakayama Hiroyuki, Doi Kunio

机构信息

Department of Veterinary Pathology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.

出版信息

Neurobiol Dis. 2005 Feb;18(1):218-25. doi: 10.1016/j.nbd.2004.09.015.

Abstract

Neural progenitor cells populate the ventricular zone of the fetal central nervous system. In this study, immediately after the administration of ethylnitrosourea (ENU), an alkylating agent, an accumulation of neural progenitor cells in the S phase was observed. This event was caused by the inhibition or arrest of DNA replication rather than acceleration of the G1/S transition. Soon after this accumulation reached its peak, the number of cells in the G2/M phase decreased and the apoptotic cell count increased. In p53-deficient mice, both ENU-induced apoptosis and S-phase accumulation were almost completely abrogated. These findings indicate that ENU inhibits or arrests DNA replication in neural progenitor cells during the S phase and then evokes apoptosis before the cells enter the G2 phase. Furthermore, these data also demonstrate that both ENU-induced apoptosis and cell cycle perturbation in the S phase require p53.

摘要

神经祖细胞聚集在胎儿中枢神经系统的脑室区。在本研究中,在给予烷基化剂乙基亚硝基脲(ENU)后,立即观察到神经祖细胞在S期的积累。该事件是由DNA复制的抑制或停滞引起的,而不是G1/S期转换的加速。在这种积累达到峰值后不久,G2/M期的细胞数量减少,凋亡细胞计数增加。在p53基因缺失的小鼠中,ENU诱导的凋亡和S期积累几乎完全消除。这些发现表明,ENU在S期抑制或阻止神经祖细胞中的DNA复制,然后在细胞进入G2期之前引发凋亡。此外,这些数据还表明,ENU诱导的凋亡和S期的细胞周期扰动都需要p53。

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