Dissociation of telomerase activity and telomere length maintenance in primitive human hematopoietic cells

被引:48
|
作者
Wang, JCY
Warner, JK
Erdmann, N
Lansdorp, PM
Harrington, L
Dick, JE [1 ]
机构
[1] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Hlth Network, Div Cell & Mol Biol, Toronto, ON M5G 2C1, Canada
[3] British Columbia Canc Agcy, Vancouver, BC V5Z 1L3, Canada
[4] Terry Fox Lab, Vancouver, BC V5Z 1L3, Canada
[5] Univ British Columbia, Dept Med, Vancouver, BC V6T 1Z4, Canada
[6] Univ Toronto, Ontario Canc Inst, Dept Med Biophys, Toronto, ON M5G 2C1, Canada
关键词
hematopoiesis; leukemogenesis;
D O I
10.1073/pnas.0504161102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Primitive human hematopoietic cells have low endogenous telomerase activity, yet telomeres are not maintained. In contrast, ectopic telomerase expression in fibroblasts and other cells leads to telomere length maintenance or elongation. It is unclear whether this disparity can be attributed to telomerase level or stems from fundamentally different telomere biology. Here, we show that telomerase overexpression does not prevent proliferation-associated telomere shortening in human hematopoietic cells, pointing to the existence of cell type-specific differences in telomere dynamics. Furthermore, we observed eventual stabilization of telomere length without detectable changes in telomerase activity during establishment of two leukemic cell lines from normal cord blood cells, indicating that additional cooperating events are required for telomere maintenance in immortalized human hematopoietic cells.
引用
收藏
页码:14398 / 14403
页数:6
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