International Journal of Hematology

DOI: 10.1007/s12185-011-0882-z Pages: 33-43

Telomere dysfunction and cell cycle checkpoints in hematopoietic stem cell aging

1. Hangzhou Normal University, School of Medicine

2. Chinese Academy of Medical Science, Tianjin Key Laboratory of Molecular Nuclear Medicine, Institute of Radiation Medicine

3. Chinese Academy of Medical Sciences, State Key Laboratory of Experimental Hematology, Institute of Hematology and Center for Stem Cell Medicine

4. University of Pittsburgh School of Medicine, Department of Radiation Oncology

Correspondence to:
Tao Cheng



Stem cells are believed to be closely associated with tissue degeneration during aging. Studies of human genetic diseases and gene-targeted animal models have provided evidence that functional decline of telomeres and deregulation of cell cycle checkpoints contribute to the aging process of tissue stem cells. Telomere dysfunction can induce DNA damage response via key cell cycle checkpoints, leading to cellular senescence or apoptosis depending on the tissue type and developmental stage of a specific stem cell compartment. Telomerase mutation and telomere shortening have been observed in a variety of hematological disorders, such as dyskeratosis congenital, aplastic anemia, myelodysplastic syndromes and leukemia, in which the hematopoietic stem cells (HSC) are a major target during the pathogenesis. Moreover, telomere dysfunction is able to induce both cell-intrinsic checkpoints and environmental factors limiting the self-renewal capacity and differentiation potential of HSCs. Crucial components in the cascade of DNA damage response, including ataxia telangiectasia mutated, CHK2, p53, p21 and p16/p19ARF, play important roles in HSC maintenance and self-renewal in the scenarios of both sufficient telomere reserve and dysfunctional telomere. Therefore, a further understanding of the molecular mechanisms underlying HSC aging may help identity new therapeutic targets for stem cell-based regenerative medicine.

To access the full text, please Sign in

If you have institutional access, please click here

Share the Knowledge