端粒酶维持正常人体细胞中的端粒结构
Kenkichi Masutomi1, Evan Y Yu, Shilagardy Khurts
1Department of Medical Oncology, Dana-Farber Cancer Institute, Brigham and Women's Hospital and Harvard Medical School, 44 Binney Street, Boston, MA 02115, USA.
Cell
|July 31, 2003
概括
人类细胞表达端粒酶 (hTERT) 的时间比想象的更早,影响细胞寿命和端粒维护. 单靠端粒长度可能不会引发细胞衰老.
科学领域:
- 细胞生物学 细胞生物学
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- 端粒缩短限制了人类正常细胞分裂.
- 细胞不朽化与端粒长度稳定有关.
- 癌细胞通常会激活端粒酶以获得不朽.
研究的目的:
- 为了研究正常人纤维细胞中的hTERT表达.
- 了解端粒酶活性在正常细胞增殖和衰老中的作用.
- 探索端粒结构和细胞寿命之间的关系.
主要方法:
- 评估循环初级存在的人类纤维细胞中的hTERT表达.
- 破坏正常人细胞中端粒酶活性.
- 分析细胞增殖率,细胞寿命和端粒维护 (包括3'悬浮).
- 监测整体端粒缩短的速度.
主要成果:
- 限制速率的端粒酶催化子单元hTERT在循环初级存在的人类纤维细胞中表达.
- 破坏端粒酶活性会减缓细胞增殖,并限制细胞寿命.
- 观察到改变了3'单链端粒突起的维持,但没有改变整体端粒缩短率.
结论:
- 端粒酶和端粒结构在正常人细胞中是动态调节的.
- 在正常细胞中,hTERT表达的时间比以前认为的更早.
- 单独的端粒长度不太可能是复制性衰老的唯一触发因素.
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