基底动态的p53显示转录减弱脉冲在循环细胞
Alexander Loewer1, Eric Batchelor, Giorgio Gaglia
1Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Cell
|July 6, 2010
概括
瘤抑制器p53通路在增殖细胞中表现出可刺激的脉冲,平衡对DNA损伤的敏感性和对暂时问题的耐受性. 这可以防止正常生长过程中不适当的细胞循环停止.
科学领域:
- 细胞生物学 细胞生物学
- 分子瘤学分子瘤学
- 遗传学 是一个遗传学.
背景情况:
- 瘤抑制剂p53对于细胞对压力的反应至关重要,包括细胞亡和细胞循环停止.
- 对于适当的细胞损伤反应,p53激活的高灵敏度是必不可少的.
- 增殖细胞面临过渡性DNA损伤,细胞循环停止或细胞亡可能是有害的.
研究的目的:
- 调查p53通路如何在增殖细胞中实现高灵敏度和耐受性对内在DNA损伤的平衡.
- 了解p53在应对细胞压力和正常生长条件时的动态行为.
主要方法:
- 量化时隔显微镜被用来监测个人人体细胞.
- 这项研究的重点是量化p53通路的基础动态在杂的细胞环境中.
主要成果:
- 增殖细胞表现出p53的自发脉冲,由细胞循环阶段与内在DNA损伤的刺激机制驱动.
- 在没有持续的损伤的情况下,翻译后修改维持了p53的不活性,防止了p21的表达和细胞循环的停止.
- 开发了一种方法来量化单个细胞的基底通路动态.
结论:
- p53通路利用一种可刺激的机制产生短暂的p53脉冲,允许对DNA损伤的敏感性,同时容忍正常的细胞噪声.
- 这种动态调节可以防止不必要的细胞循环停止,这对于有效的细胞增殖至关重要.
- 量化方法可用于研究复杂细胞环境中的其他敏感通路.
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